Portal Investigación UEx

Aminopyrine N-Demethylase Activity In Human Liver Microsomes.

Serum Concentrations Of Cytokines In Patients With Restless Legs Syndrome

Copper, Ceruloplasmin, Zinc, And Manganese Levels In Brain And Biological Fluids From Parkinson’s Disease Patients: Systematic Review And Meta-Analysis

Serum Concentrations Of Cytokines In Patients With Restless Legs Syndrome

Copper, Ceruloplasmin, Zinc, And Manganese Levels In Brain And Biological Fluids From Parkinson’s Disease Patients: Systematic Review And Meta-Analysis

Napqi Adducts In Patients With Selective Hypersensitivity To Acetaminophen

Copper, Ceruloplasmin, Zinc, And Manganese Levels In Brain And Biological Fluids From Parkinson’s Disease Patients: Systematic Review And Meta-Analysis

Napqi Adducts In Patients With Selective Hypersensitivity To Acetaminophen

Copy Number Variant Duplications Associated With Essential Tremor

Napqi Adducts In Patients With Selective Hypersensitivity To Acetaminophen

Copy Number Variant Duplications Associated With Essential Tremor

Oxidative Stress And Genetic Susceptibility To Cross-Reactive And Selective Nsaid Hypersensitivity.

Copy Number Variant Duplications Associated With Essential Tremor

Oxidative Stress And Genetic Susceptibility To Cross-Reactive And Selective Nsaid Hypersensitivity.

Potential Of Pharmacogenetics In Treatment Of Chronic Inflammatory Diseases – A Danish Report Overview From 2000 – 2024

Oxidative Stress And Genetic Susceptibility To Cross-Reactive And Selective Nsaid Hypersensitivity.

Potential Of Pharmacogenetics In Treatment Of Chronic Inflammatory Diseases – A Danish Report Overview From 2000 – 2024

Oxidative Stress In Huntington’s Disease

Potential Of Pharmacogenetics In Treatment Of Chronic Inflammatory Diseases – A Danish Report Overview From 2000 – 2024

Oxidative Stress In Huntington’s Disease

Essential Tremor - Drug Treatments Present And Future

Oxidative Stress In Huntington’s Disease

Essential Tremor - Drug Treatments Present And Future

Mdga1 Gene Variants And Risk For Restless Legs Syndrome

Essential Tremor - Drug Treatments Present And Future

Mdga1 Gene Variants And Risk For Restless Legs Syndrome

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii

Mdga1 Gene Variants And Risk For Restless Legs Syndrome

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii

Pharmvar Genefocus: Nat2—genetic Variation And Updated Nomenclature

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii

Pharmvar Genefocus: Nat2—genetic Variation And Updated Nomenclature

Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia

Pharmvar Genefocus: Nat2—genetic Variation And Updated Nomenclature

Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia

Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy

Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia

Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy

Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions

Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy

Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions

Oxidative Stress And Migraine

Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions

Oxidative Stress And Migraine

Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions

Oxidative Stress And Migraine

Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions

Oxidative Stress Markers In Multiple Sclerosis

Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions

Oxidative Stress Markers In Multiple Sclerosis

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy

Oxidative Stress Markers In Multiple Sclerosis

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy

Antioxidant Therapies In The Treatment Of Multiple Sclerosis

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy

Antioxidant Therapies In The Treatment Of Multiple Sclerosis

Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor

Antioxidant Therapies In The Treatment Of Multiple Sclerosis

Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023

Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023

Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023

Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine

Clinical Pharmacogenomics In Asthma Therapy

Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine

Clinical Pharmacogenomics In Asthma Therapy

Sleep Disorders In Patients With Choreic Syndromes

Clinical Pharmacogenomics In Asthma Therapy

Sleep Disorders In Patients With Choreic Syndromes

Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine

Sleep Disorders In Patients With Choreic Syndromes

Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine

Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions

Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine

Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics

Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics

An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease

Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics

An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease

Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting

An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease

Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis

Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis

Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis

Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine

Coenzyme Q10 And Dementia: A Systematic Review

Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine

Coenzyme Q10 And Dementia: A Systematic Review

Fármacos Antineoplásicos

Coenzyme Q10 And Dementia: A Systematic Review

Fármacos Antineoplásicos

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.

Fármacos Antineoplásicos

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.

Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis

Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.

Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis

Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome

Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis

Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome

Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease

Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome

Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease

Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review

Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease

Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review

Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor

Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review

Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor

Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine

Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor

Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine

Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man

Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine

Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021

Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021

Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome

Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021

Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome

Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis

Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome

Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis

Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives

Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis

Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives

Molecular Monitoring Of Patient Response To Painkiller Drugs

Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives

Molecular Monitoring Of Patient Response To Painkiller Drugs

Pharmvar Genefocus: Cyp2c9

Molecular Monitoring Of Patient Response To Painkiller Drugs

Pharmvar Genefocus: Cyp2c9

Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review

Pharmvar Genefocus: Cyp2c9

Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review

Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema

Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review

Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema

Pharmvar Genefocus: Cyp2c19

Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema

Pharmvar Genefocus: Cyp2c19

Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases

Pharmvar Genefocus: Cyp2c19

Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases

Editorial: Nsaids Pharmacogenomics

Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases

Editorial: Nsaids Pharmacogenomics

Current Treatment Options For Rem Sleep Behaviour Disorder

Editorial: Nsaids Pharmacogenomics

Current Treatment Options For Rem Sleep Behaviour Disorder

Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids

Current Treatment Options For Rem Sleep Behaviour Disorder

Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids

Neurochemical Features Of Rem Sleep Behaviour Disorder

Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids

Neurochemical Features Of Rem Sleep Behaviour Disorder

Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis

Neurochemical Features Of Rem Sleep Behaviour Disorder

Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis

Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk

Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis

Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk

Sleep Disorders In Patients With Essential Tremor

Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk

Sleep Disorders In Patients With Essential Tremor

Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)

Sleep Disorders In Patients With Essential Tremor

Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome

Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome

Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome

Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis

Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis

Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis

Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome

Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions

Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome

Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.

Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.

Genomic Markers For Essential Tremor

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.

Genomic Markers For Essential Tremor

Exome-Wide Rare Variant Analysis In Familial Essential Tremor

Genomic Markers For Essential Tremor

Exome-Wide Rare Variant Analysis In Familial Essential Tremor

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs

Exome-Wide Rare Variant Analysis In Familial Essential Tremor

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs

Pharmvar Genefocus: Cyp2d6

Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs

Pharmvar Genefocus: Cyp2d6

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.

Pharmvar Genefocus: Cyp2d6

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.

Exome-Wide Rare Variant Analysis In Familial Essential Tremor.

Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.

Exome-Wide Rare Variant Analysis In Familial Essential Tremor.

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.

Exome-Wide Rare Variant Analysis In Familial Essential Tremor.

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.

Pharmvar Genefocus: Cyp2c19.

Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.

Pharmvar Genefocus: Cyp2c19.

The Spanish Multidisciplinary Research Network For Allergic Diseases.

Pharmvar Genefocus: Cyp2c19.

The Spanish Multidisciplinary Research Network For Allergic Diseases.

Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5

The Spanish Multidisciplinary Research Network For Allergic Diseases.

Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5

Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs

Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5

Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs

Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?

Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs

Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis

Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis

Sleep Disorders In Tourette Syndrome

Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis

Sleep Disorders In Tourette Syndrome

Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital

Sleep Disorders In Tourette Syndrome

Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital

Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis

Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital

Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis

Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis

Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis

Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine

Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine

An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine

An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding

Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor

An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding

Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor

An Update On The Neurochemistry Of Essential Tremor

Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor

An Update On The Neurochemistry Of Essential Tremor

Pharmvar Genefocus: Cyp2d6.

An Update On The Neurochemistry Of Essential Tremor

Pharmvar Genefocus: Cyp2d6.

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.

Pharmvar Genefocus: Cyp2d6.

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.

Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients

Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.

Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients

Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury

Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients

Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury

The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer

Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury

The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer

Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer

Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

Neurochemical Features Of Idiopathic Restless Legs Syndrome

Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

Neurochemical Features Of Idiopathic Restless Legs Syndrome

Association Between Restless Legs Syndrome And Other Movement Disorders

Neurochemical Features Of Idiopathic Restless Legs Syndrome

Association Between Restless Legs Syndrome And Other Movement Disorders

Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women

Association Between Restless Legs Syndrome And Other Movement Disorders

Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women

Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor

Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women

Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor

Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy

Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor

Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy

An Update On The Neurochemistry Of Essential Tremor.

Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy

An Update On The Neurochemistry Of Essential Tremor.

Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.

An Update On The Neurochemistry Of Essential Tremor.

Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.

Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs

Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.

Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs

The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol

Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs

The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol

Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels

The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol

Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels

Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome

Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels

Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome

Genetics Of Restless Legs Syndrome: An Update

Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome

Genetics Of Restless Legs Syndrome: An Update

Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine

Genetics Of Restless Legs Syndrome: An Update

Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo

Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo

Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo

Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective

Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies

Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective

Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies

Foreword

Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies

Foreword

Genetics Of Restless Legs Syndrome: An Update.

Foreword

Genetics Of Restless Legs Syndrome: An Update.

Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome

Genetics Of Restless Legs Syndrome: An Update.

Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine

Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine

Editorial: Biomarkers In Drug Hypersensitivity

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine

Editorial: Biomarkers In Drug Hypersensitivity

Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor

Editorial: Biomarkers In Drug Hypersensitivity

Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor

Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome

Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor

Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron

Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy

Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified

Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy

Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified

7th Drug Hypersensitivity Meeting: Part One

Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified

7th Drug Hypersensitivity Meeting: Part One

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.

7th Drug Hypersensitivity Meeting: Part One

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.

Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.

Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.

A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor

Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.

A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor

Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids

A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor

Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids

Pharmacogenomics Of Prostaglandin And Leukotriene Receptors

Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids

Pharmacogenomics Of Prostaglandin And Leukotriene Receptors

Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase

Pharmacogenomics Of Prostaglandin And Leukotriene Receptors

Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase

Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase

Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects

Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis

Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease

Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease

Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease

An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease

Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease

Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives

Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease

Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives

Allergic Reactions To Metamizole: Immediate And Delayed Responses

Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives

Allergic Reactions To Metamizole: Immediate And Delayed Responses

Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease

Allergic Reactions To Metamizole: Immediate And Delayed Responses

Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease

Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole

Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease

Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole

Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study

Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole

Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis

Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis

A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis

A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels

The Genetics Of Drug Hypersensitivity Reactions

A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels

The Genetics Of Drug Hypersensitivity Reactions

Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema

The Genetics Of Drug Hypersensitivity Reactions

Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema

Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins

Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema

Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins

New Advances In The Study Of Ige Drug Recognition

Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins

New Advances In The Study Of Ige Drug Recognition

Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting

New Advances In The Study Of Ige Drug Recognition

Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis

Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population

Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis

Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population

The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis

Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population

The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine

The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine

Drug Metabolism And Hypersensitivity Reactions To Drugs

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine

Drug Metabolism And Hypersensitivity Reactions To Drugs

Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis

Drug Metabolism And Hypersensitivity Reactions To Drugs

Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome

Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome

The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor

Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome

The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor

Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor

The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor

Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor

Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor

Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor

Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome

Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome

Treatment Options For Idiopathic Restless Legs Syndrome

Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome

Treatment Options For Idiopathic Restless Legs Syndrome

Neurochemistry Of Idiopathic Restless Legs Syndrome

Treatment Options For Idiopathic Restless Legs Syndrome

Neurochemistry Of Idiopathic Restless Legs Syndrome

Pharmacogenomics Of Cyclooxygenases

Neurochemistry Of Idiopathic Restless Legs Syndrome

Pharmacogenomics Of Cyclooxygenases

Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)

Pharmacogenomics Of Cyclooxygenases

Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)

Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study

Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)

Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.

Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir

Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.

Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes

Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.

Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes

Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole

Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes

Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole

Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease

Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole

Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease

Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue

Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease

Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue

Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis

Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue

Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis

Slc1a2 Rs3794087 Variant And Risk For Migraine

Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis

Slc1a2 Rs3794087 Variant And Risk For Migraine

Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs

Slc1a2 Rs3794087 Variant And Risk For Migraine

Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs

Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs

Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Importance Of Cyp2d6 Genotype/activity Testing And Applications

Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Importance Of Cyp2d6 Genotype/activity Testing And Applications

The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome

Importance Of Cyp2d6 Genotype/activity Testing And Applications

The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome

An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease

The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome

An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease

Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs

An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease

Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs

Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs

Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America

Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis

Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America

Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease

Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America

Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease

Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting

Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease

Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting

Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions

Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting

Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions

Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process

Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions

Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process

Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine

Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process

Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.

Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.

Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.

Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.

Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases

Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C

Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases

Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C

Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations

Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C

Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations

Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis

Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations

Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis

Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis

Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis

Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis

Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome

Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis

Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?

Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia

Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?

Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome

Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?

Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome

No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population

Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome

No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population

Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts

No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population

Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts

Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans

Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts

Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans

Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome

Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans

Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome

Update On Genetics Of Essential Tremor

Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome

Update On Genetics Of Essential Tremor

Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis

Update On Genetics Of Essential Tremor

Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis

Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids

Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis

Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids

Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic

Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids

Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic

High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity

Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic

High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity

Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.

High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity

Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.

Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C

Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.

Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C

Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain

Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C

Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations

Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk

Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations

Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk

Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria

Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk

Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria

The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs

Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria

The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs

Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology

The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs

Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology

The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype

Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology

The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype

H1-Mapt And The Risk For Familial Essential Tremor

The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype

H1-Mapt And The Risk For Familial Essential Tremor

Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808

H1-Mapt And The Risk For Familial Essential Tremor

Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808

Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis

Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808

Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis

Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease

Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis

Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease

Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma

Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease

Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor

Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data

Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population

Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data

Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.

Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.

Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing

The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.

Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .

Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .

Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor

The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .

Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor

Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity

Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor

Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity

Influence Of Age And Gender In Motor Performance In Healthy Subjects

Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity

Influence Of Age And Gender In Motor Performance In Healthy Subjects

Lingo1 Gene Analysis In Parkinson's Disease Phenotypes

Influence Of Age And Gender In Motor Performance In Healthy Subjects

Lingo1 Gene Analysis In Parkinson's Disease Phenotypes

Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles

Lingo1 Gene Analysis In Parkinson's Disease Phenotypes

Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles

A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease

Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles

A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease

Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor

A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease

Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor

Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor

Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor

Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor

N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians

Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor

N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians

Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing

N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians

Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing

Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test

Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing

Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test

Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response

Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test

Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk

Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos

Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk

Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos

Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis

Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos

Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine

Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine

Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine

Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine

Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma

Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine

Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma

Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury

Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma

Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury

Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes

Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury

Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes

Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis

Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes

Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor

Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor

Alcohol Dehydrogenase 2 Genotype And Risk For Migraine

Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor

Alcohol Dehydrogenase 2 Genotype And Risk For Migraine

Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease

Alcohol Dehydrogenase 2 Genotype And Risk For Migraine

Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease

Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome

Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease

Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome

Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))

Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome

Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))

Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor

Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))

Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor

Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.

Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor

Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.

Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease

Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.

Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease

Pharmacogenomics In Drug Induced Liver Injury

Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease

Pharmacogenomics In Drug Induced Liver Injury

Pharmacogenomics In Aspirin Intolerance

Pharmacogenomics In Drug Induced Liver Injury

Pharmacogenomics In Aspirin Intolerance

Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor

Pharmacogenomics In Aspirin Intolerance

Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor

Histamine Pharmacogenomics

Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor

Histamine Pharmacogenomics

Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?

Histamine Pharmacogenomics

Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?

Polymorphic Drug Metabolism In Anaesthesia

Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?

Polymorphic Drug Metabolism In Anaesthesia

Reply

Polymorphic Drug Metabolism In Anaesthesia

Reply

Current Drug Metabolism: Editorial

Reply

Current Drug Metabolism: Editorial

Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs

Current Drug Metabolism: Editorial

Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs

Motor Performance In Patients With Restless Legs Syndrome

Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs

Motor Performance In Patients With Restless Legs Syndrome

Recent Advances In Drug Intolerance.

Motor Performance In Patients With Restless Legs Syndrome

Recent Advances In Drug Intolerance.

The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor

Recent Advances In Drug Intolerance.

The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor

Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor

Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission

Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission

Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury

Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission

Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury

Unraveling Ambiguous Nat2 Genotyping Data

Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury

Unraveling Ambiguous Nat2 Genotyping Data

Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease

Unraveling Ambiguous Nat2 Genotyping Data

Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease

Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease

Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease

Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease

Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor

Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease

Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor

Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding

Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor

Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding

Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer

Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding

Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer

Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research

Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer

Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research

Polymorphisms Of Human N-Acetyltransferases And Cancer Risk

Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research

Polymorphisms Of Human N-Acetyltransferases And Cancer Risk

A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3

Polymorphisms Of Human N-Acetyltransferases And Cancer Risk

A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3

Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles

A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3

Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles

Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients

Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles

Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients

Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.

Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients

Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.

Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.

Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.

Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.

Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.

Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity

Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals

Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity

Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans

Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity

Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans

Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis

Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans

Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis

Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor

Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis

Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor

Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic

Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor

Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic

Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding

Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic

Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding

Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor

Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding

Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor

[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]

Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor

[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]

The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma

[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]

The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma

Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia

The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma

Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia

Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma

Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia

Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma

Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene

Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma

Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene

Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids

Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene

Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids

Cyp2c19 Polymorphism And Risk For Essential Tremor

Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids

Cyp2c19 Polymorphism And Risk For Essential Tremor

Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals

Cyp2c19 Polymorphism And Risk For Essential Tremor

Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals

Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population

Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals

Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population

Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans

Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population

Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans

Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8

Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans

Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8

The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases

Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8

The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases

Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication

The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases

Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication

Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids

Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication

Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids

Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease

Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids

Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease

The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects

Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease

The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects

Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease

The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects

Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease

Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms

Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease

Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms

Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use

Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms

Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use

Cytochrome P450 Gene Polymorphism And Cancer

Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use

Cytochrome P450 Gene Polymorphism And Cancer

Leflunomide-Induced Acute Hepatitis

Cytochrome P450 Gene Polymorphism And Cancer

Leflunomide-Induced Acute Hepatitis

High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region

Leflunomide-Induced Acute Hepatitis

High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region

Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses

High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region

Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses

Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk

Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses

Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk

Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity

Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk

Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity

Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy

Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity

Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy

Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease

Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy

Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease

N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease

Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease

N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease

N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma

N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease

N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma

High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population

N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma

High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population

Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk

High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population

Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk

Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada

Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk

Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada

C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease

Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada

C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease

Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline

C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease

Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline

Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients

Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline

Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients

N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?

Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients

N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?

Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors

N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?

Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors

Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients

Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors

Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients

Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists

Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients

Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists

Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism

Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists

Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism

Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.

Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism

Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.

Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a

Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.

Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a

Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population

Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a

Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population

Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease

Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population

Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease

Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk

Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease

Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk

Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine

Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk

Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine

Polimorfismos Enzimáticos Y Cáncer De Pulmón

Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine

Polimorfismos Enzimáticos Y Cáncer De Pulmón

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]

Polimorfismos Enzimáticos Y Cáncer De Pulmón

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]

Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]

Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe

Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians

Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe

Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians

Hallevorden-Spatz Disease

Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians

Hallevorden-Spatz Disease

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

Hallevorden-Spatz Disease

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine

Polymorphism Is Not Associated With Essential Tremor

Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine

Polymorphism Is Not Associated With Essential Tremor

Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis

Polymorphism Is Not Associated With Essential Tremor

Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis

Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus

Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis

Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus

Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population

Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus

Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population

Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]

Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population

Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]

Cyp2d6 Genotypes In Spanish Women With Breast Cancer

Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]

Cyp2d6 Genotypes In Spanish Women With Breast Cancer

Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine

Cyp2d6 Genotypes In Spanish Women With Breast Cancer

Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine

Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease

Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine

Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease

Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma

Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease

Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma

Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers

Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma

Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers

Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine

Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers

Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine

Cyp2d6 Genes And Risk Of Liver Cancer

Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine

Cyp2d6 Genes And Risk Of Liver Cancer

Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus

Cyp2d6 Genes And Risk Of Liver Cancer

Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus

Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways

Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus

Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways

Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease

Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways

Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease

Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients

Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease

Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients

Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population

Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients

Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population

Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis

Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population

Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis

Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis

Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis

Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis

Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography

Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis

Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations

Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.

Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.

Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.

Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype

Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.

Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype

Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity

Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype

Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity

Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody

Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity

Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody

Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases

Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody

Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases

Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine

Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases

Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine

Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy

Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine

Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy

Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate

Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy

Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate

Aminopyrine N-Demethylase Activity In Human Liver Microsomes

Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate

Aminopyrine N-Demethylase Activity In Human Liver Microsomes

Aminopyrine N-Demethylase Activity In Human Liver Microsomes.

Aminopyrine N-Demethylase Activity In Human Liver Microsomes

Aminopyrine N-Demethylase Activity In Human Liver Microsomes.

Serum Concentrations Of Cytokines In Patients With Restless Legs Syndrome