Portal Investigación UEx

Tamaño De La Fontanela En El Recién Nacido Normal. Relación Con Parámetros Antropométricos Y Bioquímicos

Prognostic Significance Of Mutation Type And Chromosome Fragility In Fanconi Anemia

Oral Administration Of Hydrolyzed Collagen Alleviates Pain And Enhances Functionality In Knee Osteoarthritis: Results From A Randomized, Double-Blind, Placebo-Controlled Study

Prognostic Significance Of Mutation Type And Chromosome Fragility In Fanconi Anemia

Oral Administration Of Hydrolyzed Collagen Alleviates Pain And Enhances Functionality In Knee Osteoarthritis: Results From A Randomized, Double-Blind, Placebo-Controlled Study

Association Of Genetic Variation In The Leptin-Melanocortin System With Drive For Thinness In Patients With Eating Disorders: A Pilot Study

Oral Administration Of Hydrolyzed Collagen Alleviates Pain And Enhances Functionality In Knee Osteoarthritis: Results From A Randomized, Double-Blind, Placebo-Controlled Study

Association Of Genetic Variation In The Leptin-Melanocortin System With Drive For Thinness In Patients With Eating Disorders: A Pilot Study

Impact Of Combined Macronutrient Diet On Amino Acids And Amines Plasma Levels

Association Of Genetic Variation In The Leptin-Melanocortin System With Drive For Thinness In Patients With Eating Disorders: A Pilot Study

Impact Of Combined Macronutrient Diet On Amino Acids And Amines Plasma Levels

Association Between Adherence To Patient Blood Management Recommendations And Postoperative Complications In Hip And Knee Arthroplasty

Impact Of Combined Macronutrient Diet On Amino Acids And Amines Plasma Levels

Association Between Adherence To Patient Blood Management Recommendations And Postoperative Complications In Hip And Knee Arthroplasty

Contaminants In Dietary Supplements: Toxicity, Doping Risk, And Current Regulation

Association Between Adherence To Patient Blood Management Recommendations And Postoperative Complications In Hip And Knee Arthroplasty

Contaminants In Dietary Supplements: Toxicity, Doping Risk, And Current Regulation

Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation

Contaminants In Dietary Supplements: Toxicity, Doping Risk, And Current Regulation

Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation

Impact Of Variability In The Delta Opioid Receptor (Oprd1) Gene On Body Mass Index And Psychometric Characteristics Of Eating Disorders Patients

Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation

Impact Of Variability In The Delta Opioid Receptor (Oprd1) Gene On Body Mass Index And Psychometric Characteristics Of Eating Disorders Patients

Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)

Impact Of Variability In The Delta Opioid Receptor (Oprd1) Gene On Body Mass Index And Psychometric Characteristics Of Eating Disorders Patients

Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)

Association Of Oprd1 Gene Variants With Changes In Body Weight And Psychometric Indicators In Patients With Eating Disorders

Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)

Association Of Oprd1 Gene Variants With Changes In Body Weight And Psychometric Indicators In Patients With Eating Disorders

Effect Of Leptin Concentrations And Leptin Receptor Gene Polymorphisms On The Outcome Of Renal Transplantation

Association Of Oprd1 Gene Variants With Changes In Body Weight And Psychometric Indicators In Patients With Eating Disorders

Effect Of Leptin Concentrations And Leptin Receptor Gene Polymorphisms On The Outcome Of Renal Transplantation

Role Of Obesity And Mediators Of Adipose Tissue In Renal Transplant And Disease

Effect Of Leptin Concentrations And Leptin Receptor Gene Polymorphisms On The Outcome Of Renal Transplantation

Role Of Obesity And Mediators Of Adipose Tissue In Renal Transplant And Disease

Haploidentical Vs. Hla-Matched Donor Hematopoietic Stem-Cell Transplantation For Pediatric Patients With Acute Lymphoblastic Leukemia In Second Remission: A Collaborative Retrospective Study Of The Spanish Group For Bone Marrow Transplantation In Children (Getmon/geth) And The Spanish Childhood Relapsed All Board (Reallnet)

Role Of Obesity And Mediators Of Adipose Tissue In Renal Transplant And Disease

Haploidentical Vs. Hla-Matched Donor Hematopoietic Stem-Cell Transplantation For Pediatric Patients With Acute Lymphoblastic Leukemia In Second Remission: A Collaborative Retrospective Study Of The Spanish Group For Bone Marrow Transplantation In Children (Getmon/geth) And The Spanish Childhood Relapsed All Board (Reallnet)

Recent Advances And Remaining Challenges In The Management Of Diabetic Kidney Disease

Haploidentical Vs. Hla-Matched Donor Hematopoietic Stem-Cell Transplantation For Pediatric Patients With Acute Lymphoblastic Leukemia In Second Remission: A Collaborative Retrospective Study Of The Spanish Group For Bone Marrow Transplantation In Children (Getmon/geth) And The Spanish Childhood Relapsed All Board (Reallnet)

Recent Advances And Remaining Challenges In The Management Of Diabetic Kidney Disease

Prognostic Significance Of Amino Acid And Biogenic Amines Profiling In Chronic Kidney Disease

Recent Advances And Remaining Challenges In The Management Of Diabetic Kidney Disease

Prognostic Significance Of Amino Acid And Biogenic Amines Profiling In Chronic Kidney Disease

Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization

Prognostic Significance Of Amino Acid And Biogenic Amines Profiling In Chronic Kidney Disease

Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization

Influence Of Variability In The Cyclooxygenase Pathway On Cardiovascular Outcomes Of Nephrosclerosis Patients

Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization

Influence Of Variability In The Cyclooxygenase Pathway On Cardiovascular Outcomes Of Nephrosclerosis Patients

Adolescent Cancer Care: What Has Changed In Spain In The Past Decade?

Influence Of Variability In The Cyclooxygenase Pathway On Cardiovascular Outcomes Of Nephrosclerosis Patients

Adolescent Cancer Care: What Has Changed In Spain In The Past Decade?

Genetic Diagnosis Of Basal Ganglia Disease In Childhood

Adolescent Cancer Care: What Has Changed In Spain In The Past Decade?

Genetic Diagnosis Of Basal Ganglia Disease In Childhood

Body Fat Distribution, Adipocytokines Levels And Variability In Associated Genes And Kidney Transplant Outcomes

Genetic Diagnosis Of Basal Ganglia Disease In Childhood

Body Fat Distribution, Adipocytokines Levels And Variability In Associated Genes And Kidney Transplant Outcomes

Tag-Snps In Phospholipase-Related Genes Modify The Susceptibility To Nephrosclerosis And Its Associated Cardiovascular Risk

Body Fat Distribution, Adipocytokines Levels And Variability In Associated Genes And Kidney Transplant Outcomes

Tag-Snps In Phospholipase-Related Genes Modify The Susceptibility To Nephrosclerosis And Its Associated Cardiovascular Risk

Polymorphisms In Glucose Homeostasis Genes Are Associated With Cardiovascular And Renal Parameters In Patients With Diabetic Nephropathy

Tag-Snps In Phospholipase-Related Genes Modify The Susceptibility To Nephrosclerosis And Its Associated Cardiovascular Risk

Polymorphisms In Glucose Homeostasis Genes Are Associated With Cardiovascular And Renal Parameters In Patients With Diabetic Nephropathy

Venous Thromboembolism In Pediatric Patients With Acute Lymphoblastic Leukemia Under Chemotherapy Treatment. Risk Factors And Usefulness Of Thromboprophylaxis. Results Of Lal-Sehop-Pethema-2013

Polymorphisms In Glucose Homeostasis Genes Are Associated With Cardiovascular And Renal Parameters In Patients With Diabetic Nephropathy

Venous Thromboembolism In Pediatric Patients With Acute Lymphoblastic Leukemia Under Chemotherapy Treatment. Risk Factors And Usefulness Of Thromboprophylaxis. Results Of Lal-Sehop-Pethema-2013

A New Case Of Acquired Haemophilia B In The Context Of Liver Autoimmune Disease

Venous Thromboembolism In Pediatric Patients With Acute Lymphoblastic Leukemia Under Chemotherapy Treatment. Risk Factors And Usefulness Of Thromboprophylaxis. Results Of Lal-Sehop-Pethema-2013

A New Case Of Acquired Haemophilia B In The Context Of Liver Autoimmune Disease

Phase 2 Clinical Trial Of Infusing Haploidentical K562-Mb15-41bbl–activated And Expanded Natural Killer Cells As Consolidation Therapy For Pediatric Acute Myeloblastic Leukemia

A New Case Of Acquired Haemophilia B In The Context Of Liver Autoimmune Disease

Phase 2 Clinical Trial Of Infusing Haploidentical K562-Mb15-41bbl–activated And Expanded Natural Killer Cells As Consolidation Therapy For Pediatric Acute Myeloblastic Leukemia

A Custom Target Next-Generation Sequencing 70-Gene Panel And Replication Study To Identify Genetic Markers Of Diabetic Kidney Disease

Phase 2 Clinical Trial Of Infusing Haploidentical K562-Mb15-41bbl–activated And Expanded Natural Killer Cells As Consolidation Therapy For Pediatric Acute Myeloblastic Leukemia

A Custom Target Next-Generation Sequencing 70-Gene Panel And Replication Study To Identify Genetic Markers Of Diabetic Kidney Disease

Variability In Cannabinoid Receptor Genes Is Associated With Psychiatric Comorbidities In Anorexia Nervosa

A Custom Target Next-Generation Sequencing 70-Gene Panel And Replication Study To Identify Genetic Markers Of Diabetic Kidney Disease

Variability In Cannabinoid Receptor Genes Is Associated With Psychiatric Comorbidities In Anorexia Nervosa

Genetics Variants In The Epoxygenase Pathway Of Arachidonic Metabolism Are Associated With Eicosanoids Levels And The Risk Of Diabetic Nephropathy

Variability In Cannabinoid Receptor Genes Is Associated With Psychiatric Comorbidities In Anorexia Nervosa

Genetics Variants In The Epoxygenase Pathway Of Arachidonic Metabolism Are Associated With Eicosanoids Levels And The Risk Of Diabetic Nephropathy

Genetic Variants In Pge2 Receptors Modulate The Risk Of Nephrosclerosis And Clinical Outcomes In These Patients

Genetics Variants In The Epoxygenase Pathway Of Arachidonic Metabolism Are Associated With Eicosanoids Levels And The Risk Of Diabetic Nephropathy

Genetic Variants In Pge2 Receptors Modulate The Risk Of Nephrosclerosis And Clinical Outcomes In These Patients

Variants In The Obesity-Linked Fto Gene Locus Modulates Psychopathological Features Of Patients With Anorexia Nervosa

Genetic Variants In Pge2 Receptors Modulate The Risk Of Nephrosclerosis And Clinical Outcomes In These Patients

Variants In The Obesity-Linked Fto Gene Locus Modulates Psychopathological Features Of Patients With Anorexia Nervosa

Genetic Variants In Dopamine Pathways Affect Personality Dimensions Displayed By Patients With Eating Disorders

Variants In The Obesity-Linked Fto Gene Locus Modulates Psychopathological Features Of Patients With Anorexia Nervosa

Genetic Variants In Dopamine Pathways Affect Personality Dimensions Displayed By Patients With Eating Disorders

Variability In The Antioxidant Msra Gene Affects The Psychopathology Of Patients With Anorexia Nervosa

Genetic Variants In Dopamine Pathways Affect Personality Dimensions Displayed By Patients With Eating Disorders

Variability In The Antioxidant Msra Gene Affects The Psychopathology Of Patients With Anorexia Nervosa

Plasma And Urinary Concentrations Of Arachidonic Acid-Derived Eicosanoids Are Associated With Diabetic Kidney Disease

Variability In The Antioxidant Msra Gene Affects The Psychopathology Of Patients With Anorexia Nervosa

Plasma And Urinary Concentrations Of Arachidonic Acid-Derived Eicosanoids Are Associated With Diabetic Kidney Disease

Sacubitril-Valsartan Improves Anemia Of Cardiorenal Syndrome (Crs)

Plasma And Urinary Concentrations Of Arachidonic Acid-Derived Eicosanoids Are Associated With Diabetic Kidney Disease

Sacubitril-Valsartan Improves Anemia Of Cardiorenal Syndrome (Crs)

Measurable Residual Disease Assessed By Flow-Cytometry Is A Stable Prognostic Factor For Pediatric T-Cell Acute Lymphoblastic Leukemia In Consecutive Sehop Protocols Whereas The Impact Of Oncogenetics Depends On Treatment

Sacubitril-Valsartan Improves Anemia Of Cardiorenal Syndrome (Crs)

Measurable Residual Disease Assessed By Flow-Cytometry Is A Stable Prognostic Factor For Pediatric T-Cell Acute Lymphoblastic Leukemia In Consecutive Sehop Protocols Whereas The Impact Of Oncogenetics Depends On Treatment

Study Protocol For A Phase Ii, Multicentre, Prospective, Non-Randomised Clinical Trial To Assess The Safety And Efficacy Of Infusing Allogeneic Activated And Expanded Natural Killer Cells As Consolidation Therapy For Paediatric Acute Myeloblastic Leukaemia

Measurable Residual Disease Assessed By Flow-Cytometry Is A Stable Prognostic Factor For Pediatric T-Cell Acute Lymphoblastic Leukemia In Consecutive Sehop Protocols Whereas The Impact Of Oncogenetics Depends On Treatment

Study Protocol For A Phase Ii, Multicentre, Prospective, Non-Randomised Clinical Trial To Assess The Safety And Efficacy Of Infusing Allogeneic Activated And Expanded Natural Killer Cells As Consolidation Therapy For Paediatric Acute Myeloblastic Leukaemia

Management Of Iron Deficiency In Various Clinical Conditions And The Role Of Intravenous Iron: Recommendations Of The Spanish Erythropathology Group Of The Spanish Society Of Haematology And Haemotherapy

Study Protocol For A Phase Ii, Multicentre, Prospective, Non-Randomised Clinical Trial To Assess The Safety And Efficacy Of Infusing Allogeneic Activated And Expanded Natural Killer Cells As Consolidation Therapy For Paediatric Acute Myeloblastic Leukaemia

Management Of Iron Deficiency In Various Clinical Conditions And The Role Of Intravenous Iron: Recommendations Of The Spanish Erythropathology Group Of The Spanish Society Of Haematology And Haemotherapy

Combined Donor-Recipient Genotypes Of Leptin Receptor And Adiponectin Gene Polymorphisms Affect The Incidence Of Complications After Renal Transplantation

Management Of Iron Deficiency In Various Clinical Conditions And The Role Of Intravenous Iron: Recommendations Of The Spanish Erythropathology Group Of The Spanish Society Of Haematology And Haemotherapy

Combined Donor-Recipient Genotypes Of Leptin Receptor And Adiponectin Gene Polymorphisms Affect The Incidence Of Complications After Renal Transplantation

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients

Combined Donor-Recipient Genotypes Of Leptin Receptor And Adiponectin Gene Polymorphisms Affect The Incidence Of Complications After Renal Transplantation

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients

Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients

Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies

C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?

Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies

C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients.

C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients.

Polymorphisms In Vasoactive Eicosanoid Genes Of Kidney Donors Affect Biopsy Scores And Clinical Outcomes In Renal Transplantation

Association Of Polymorphisms In Leptin And Adiponectin Genes With Long-Term Outcomes In Renal Transplant Recipients.

Polymorphisms In Vasoactive Eicosanoid Genes Of Kidney Donors Affect Biopsy Scores And Clinical Outcomes In Renal Transplantation

Pharmacogenetics And Personalized Medicine. Are Expectations Being Met?

Polymorphisms In Vasoactive Eicosanoid Genes Of Kidney Donors Affect Biopsy Scores And Clinical Outcomes In Renal Transplantation

Pharmacogenetics And Personalized Medicine. Are Expectations Being Met?

Variability In The Leptin Receptor Gene And Other Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant Recipients

Pharmacogenetics And Personalized Medicine. Are Expectations Being Met?

Variability In The Leptin Receptor Gene And Other Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant Recipients

Clinical Implications Of Methotrexate Pharmacogenetics In Childhood Acute Lymphoblastic Leukaemia

Variability In The Leptin Receptor Gene And Other Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant Recipients

Clinical Implications Of Methotrexate Pharmacogenetics In Childhood Acute Lymphoblastic Leukaemia

Expanding The Clinical And Genetic Spectra Of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected And Unexpected Findings

Clinical Implications Of Methotrexate Pharmacogenetics In Childhood Acute Lymphoblastic Leukaemia

Expanding The Clinical And Genetic Spectra Of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected And Unexpected Findings

Burkitt-Like Lymphoma With 11q Aberration: A Germinal Center-Derived Lymphoma Genetically Unrelated To Burkitt Lymphoma

Expanding The Clinical And Genetic Spectra Of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected And Unexpected Findings

Burkitt-Like Lymphoma With 11q Aberration: A Germinal Center-Derived Lymphoma Genetically Unrelated To Burkitt Lymphoma

Effect Of Dopamine Receptor D4 (Drd4) Haplotypes On General Psychopathology In Patients With Eating Disorders

Burkitt-Like Lymphoma With 11q Aberration: A Germinal Center-Derived Lymphoma Genetically Unrelated To Burkitt Lymphoma

Effect Of Dopamine Receptor D4 (Drd4) Haplotypes On General Psychopathology In Patients With Eating Disorders

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients

Effect Of Dopamine Receptor D4 (Drd4) Haplotypes On General Psychopathology In Patients With Eating Disorders

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients

Association Of Comt Val158met Polymorphism With Psychopathological Symptoms In Patients With Eating Disorders

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients

Association Of Comt Val158met Polymorphism With Psychopathological Symptoms In Patients With Eating Disorders

Cyp3a Genotypes Of Donors But Not Those Of The Patients Increase The Risk Of Acute Rejection In Renal Transplant Recipients On Calcineurin Inhibitors: A Pilot Study

Association Of Comt Val158met Polymorphism With Psychopathological Symptoms In Patients With Eating Disorders

Cyp3a Genotypes Of Donors But Not Those Of The Patients Increase The Risk Of Acute Rejection In Renal Transplant Recipients On Calcineurin Inhibitors: A Pilot Study

Recomendaciones Para El Abordaje Del Déficit De Hierro: Papel Del Hierro Intravenoso

Cyp3a Genotypes Of Donors But Not Those Of The Patients Increase The Risk Of Acute Rejection In Renal Transplant Recipients On Calcineurin Inhibitors: A Pilot Study

Recomendaciones Para El Abordaje Del Déficit De Hierro: Papel Del Hierro Intravenoso

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients.

Recomendaciones Para El Abordaje Del Déficit De Hierro: Papel Del Hierro Intravenoso

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients.

Research Update For Articles Published In Ejci In 2015

Polymorphisms In Genes Involved In Vasoactive Eicosanoid Synthesis Affect Cardiovascular Risk In Renal Transplant Recipients.

Research Update For Articles Published In Ejci In 2015

Effect Of Polymorphisms In Transporter Genes On Dosing, Efficacy And Toxicity Of Maintenance Therapy In Children With Acute Lymphoblastic Leukemia

Research Update For Articles Published In Ejci In 2015

Effect Of Polymorphisms In Transporter Genes On Dosing, Efficacy And Toxicity Of Maintenance Therapy In Children With Acute Lymphoblastic Leukemia

Influence Of Tfap2b And Kctd15 Genetic Variability On Personality Dimensions In Anorexia And Bulimia Nervosa

Effect Of Polymorphisms In Transporter Genes On Dosing, Efficacy And Toxicity Of Maintenance Therapy In Children With Acute Lymphoblastic Leukemia

Influence Of Tfap2b And Kctd15 Genetic Variability On Personality Dimensions In Anorexia And Bulimia Nervosa

Potential Beneficial Effects Of Sacubitril-Valsartan In Renal Disease: A New Field For A New Drug

Influence Of Tfap2b And Kctd15 Genetic Variability On Personality Dimensions In Anorexia And Bulimia Nervosa

Potential Beneficial Effects Of Sacubitril-Valsartan In Renal Disease: A New Field For A New Drug

Polymorphisms In The Snrpn Gene Are Associated With Obesity Susceptibility In A Spanish Population

Potential Beneficial Effects Of Sacubitril-Valsartan In Renal Disease: A New Field For A New Drug

Polymorphisms In The Snrpn Gene Are Associated With Obesity Susceptibility In A Spanish Population

Different Distribution Of The Common Hfe Variants Between Western And Eastern Spanish Populations Evidences An Independent Haplotype Gene Flow

Polymorphisms In The Snrpn Gene Are Associated With Obesity Susceptibility In A Spanish Population

Different Distribution Of The Common Hfe Variants Between Western And Eastern Spanish Populations Evidences An Independent Haplotype Gene Flow

Dihydrofolate Reductase Genetic Polymorphisms Affect Methotrexate Dose Requirements In Pediatric Patients With Acute Lymphoblastic Leukemia On Maintenance Therapy

Different Distribution Of The Common Hfe Variants Between Western And Eastern Spanish Populations Evidences An Independent Haplotype Gene Flow

Dihydrofolate Reductase Genetic Polymorphisms Affect Methotrexate Dose Requirements In Pediatric Patients With Acute Lymphoblastic Leukemia On Maintenance Therapy

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients

Dihydrofolate Reductase Genetic Polymorphisms Affect Methotrexate Dose Requirements In Pediatric Patients With Acute Lymphoblastic Leukemia On Maintenance Therapy

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients

Blastic Plasmacytoid Dendritic Cell Neoplasm

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients

Blastic Plasmacytoid Dendritic Cell Neoplasm

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients.

Blastic Plasmacytoid Dendritic Cell Neoplasm

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients.

Etiopathological Mechanisms And Clinical Characteristics Of Hyperhemolysis Syndrome In Spanish Patients With Thalassemia

Polymorphisms In Abcb1 And Cyp19a1 Genes Affect Anastrozole Plasma Concentrations And Clinical Outcomes In Postmenopausal Breast Cancer Patients.

Etiopathological Mechanisms And Clinical Characteristics Of Hyperhemolysis Syndrome In Spanish Patients With Thalassemia

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism

Etiopathological Mechanisms And Clinical Characteristics Of Hyperhemolysis Syndrome In Spanish Patients With Thalassemia

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism

Congenital Dyserythropoietic Anemia Associated To A Gata1 Mutation Aggravated By Pyruvate Kinase Deficiency

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism

Congenital Dyserythropoietic Anemia Associated To A Gata1 Mutation Aggravated By Pyruvate Kinase Deficiency

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism.

Congenital Dyserythropoietic Anemia Associated To A Gata1 Mutation Aggravated By Pyruvate Kinase Deficiency

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism.

Management And Monitoring Of Patients With Duchenne Disease

Risk Factors For Post-Transplant Diabetes Mellitus In Renal Transplant: Role Of Genetic Variability In The Cyp450-Mediated Arachidonic Acid Metabolism.

Management And Monitoring Of Patients With Duchenne Disease

Polymorphisms In Cyp-Mediated Arachidonic Acid Routes Affect The Outcome Of Renal Transplantation

Management And Monitoring Of Patients With Duchenne Disease

Polymorphisms In Cyp-Mediated Arachidonic Acid Routes Affect The Outcome Of Renal Transplantation

A 3′-Utr Polymorphism In Soluble Epoxide Hydrolase Gene Is Associated With Acute Rejection In Renal Transplant Recipients

Polymorphisms In Cyp-Mediated Arachidonic Acid Routes Affect The Outcome Of Renal Transplantation

A 3′-Utr Polymorphism In Soluble Epoxide Hydrolase Gene Is Associated With Acute Rejection In Renal Transplant Recipients

Discussing The Putative Role Of Obesity-Associated Genes In The Etiopathogenesis Of Eating Disorders

A 3′-Utr Polymorphism In Soluble Epoxide Hydrolase Gene Is Associated With Acute Rejection In Renal Transplant Recipients

Discussing The Putative Role Of Obesity-Associated Genes In The Etiopathogenesis Of Eating Disorders

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders

Discussing The Putative Role Of Obesity-Associated Genes In The Etiopathogenesis Of Eating Disorders

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders

Functional Consequences Of Transferrin Receptor-2 Mutations Causing Hereditary Hemochromatosis Type 3

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders

Functional Consequences Of Transferrin Receptor-2 Mutations Causing Hereditary Hemochromatosis Type 3

Clinical Relevance Of Erythrocyte Ferritin In Microcytic Anemias

Functional Consequences Of Transferrin Receptor-2 Mutations Causing Hereditary Hemochromatosis Type 3

Clinical Relevance Of Erythrocyte Ferritin In Microcytic Anemias

Melanocortin-4 Receptor Gene Variants Are Not Associated With Binge-Eating Behavior In Nonobese Patients With Eating Disorders

Clinical Relevance Of Erythrocyte Ferritin In Microcytic Anemias

Melanocortin-4 Receptor Gene Variants Are Not Associated With Binge-Eating Behavior In Nonobese Patients With Eating Disorders

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders.

Melanocortin-4 Receptor Gene Variants Are Not Associated With Binge-Eating Behavior In Nonobese Patients With Eating Disorders

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders.

Thalassemia Diagnosis In A Blood Donor From A Unique Trimorphic Red Blood Cell Population Observed In The Recipient

Impact Of Negr1 Genetic Variability On Psychological Traits Of Patients With Eating Disorders.

Thalassemia Diagnosis In A Blood Donor From A Unique Trimorphic Red Blood Cell Population Observed In The Recipient

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms

Thalassemia Diagnosis In A Blood Donor From A Unique Trimorphic Red Blood Cell Population Observed In The Recipient

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders

Diagnostic And Therapeutic Challenges Of Primary Autoimmune Haemolytic Anaemia In Children

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders

Diagnostic And Therapeutic Challenges Of Primary Autoimmune Haemolytic Anaemia In Children

Novel Variants In The Mc4r And Lepr Genes Among Severely Obese Children From The Iberian Population

Diagnostic And Therapeutic Challenges Of Primary Autoimmune Haemolytic Anaemia In Children

Novel Variants In The Mc4r And Lepr Genes Among Severely Obese Children From The Iberian Population

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders.

Novel Variants In The Mc4r And Lepr Genes Among Severely Obese Children From The Iberian Population

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders.

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms.

Bdnf Genetic Variability Modulates Psychopathological Symptoms In Patients With Eating Disorders.

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms.

Relevancia De Los Polimorfismos Genéticos En La Respuesta Farmacológica

Hyperhaemolysis Syndrome Responsive To Splenectomy In A Patient With Δβ-Thalassaemia: A Discussion On Underlying Mechanisms.

Relevancia De Los Polimorfismos Genéticos En La Respuesta Farmacológica

Ethylenediaminetetraacetic Acid-Dependent Pseudomacrocytosis

Relevancia De Los Polimorfismos Genéticos En La Respuesta Farmacológica

Ethylenediaminetetraacetic Acid-Dependent Pseudomacrocytosis

Influence Of Dopamine Polymorphisms On The Risk For Anorexia Nervosa And Associated Psychopathological Features

Ethylenediaminetetraacetic Acid-Dependent Pseudomacrocytosis

Influence Of Dopamine Polymorphisms On The Risk For Anorexia Nervosa And Associated Psychopathological Features

Cyp2c83 Polymorphism And Donor Age Are Associated With Allograft Dysfunction In Kidney Transplant Recipients Treated With Calcineurin Inhibitors

Influence Of Dopamine Polymorphisms On The Risk For Anorexia Nervosa And Associated Psychopathological Features

Cyp2c83 Polymorphism And Donor Age Are Associated With Allograft Dysfunction In Kidney Transplant Recipients Treated With Calcineurin Inhibitors

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients

Cyp2c83 Polymorphism And Donor Age Are Associated With Allograft Dysfunction In Kidney Transplant Recipients Treated With Calcineurin Inhibitors

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients

Haplotypes In The 5′-Untranslated Region Of The Cyp1a2gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients

Haplotypes In The 5′-Untranslated Region Of The Cyp1a2gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia

Haplotypes In The 5′-Untranslated Region Of The Cyp1a2gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia

Comparative Cytochrome P450 In Vitro Inhibition By Atypical Antipsychotic Drugs.

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia

Comparative Cytochrome P450 In Vitro Inhibition By Atypical Antipsychotic Drugs.

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia.

Comparative Cytochrome P450 In Vitro Inhibition By Atypical Antipsychotic Drugs.

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia.

Haplotypes In The 5'-Untranslated Region Of The Cyp1a2 Gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism.

Diagnostic Utility Of Hfe Variants In Spanish Patients: Association With Hla Alleles And Role In Susceptibility To Acute Lymphoblastic Leukemia.

Haplotypes In The 5'-Untranslated Region Of The Cyp1a2 Gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism.

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients.

Haplotypes In The 5'-Untranslated Region Of The Cyp1a2 Gene Are Inversely Associated With Lung Cancer Risk But Do Not Correlate With Caffeine Metabolism.

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients.

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

Abcb1 Polymorphisms Are Associated With Cyclosporine-Induced Nephrotoxicity And Gingival Hyperplasia In Renal Transplant Recipients.

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

Impact Of Genetic Polymorphisms On Chemotherapy Toxicity In Childhood Acute Lymphoblastic Leukemia

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

Impact Of Genetic Polymorphisms On Chemotherapy Toxicity In Childhood Acute Lymphoblastic Leukemia

Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma

Impact Of Genetic Polymorphisms On Chemotherapy Toxicity In Childhood Acute Lymphoblastic Leukemia

Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma

Polymorphisms In Serotonergic Genes And Psychopathological Traits In Eating Disorders

Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma

Polymorphisms In Serotonergic Genes And Psychopathological Traits In Eating Disorders

Impact Of Genetic Polymorphisms On Tacrolimus Pharmacokinetics And The Clinical Outcome Of Renal Transplantation

Polymorphisms In Serotonergic Genes And Psychopathological Traits In Eating Disorders

Impact Of Genetic Polymorphisms On Tacrolimus Pharmacokinetics And The Clinical Outcome Of Renal Transplantation

A Neutron Diagnostic For High Current Deuterium Beams.

Impact Of Genetic Polymorphisms On Tacrolimus Pharmacokinetics And The Clinical Outcome Of Renal Transplantation

A Neutron Diagnostic For High Current Deuterium Beams.

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population

A Neutron Diagnostic For High Current Deuterium Beams.

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population

Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population

Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis

Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties

Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis

Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Cyp1a1 Gene Polymorphisms Increase Lung Cancer Risk In A High-Incidence Region Of Spain: A Case Control Study

Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis

Cyp1a1 Gene Polymorphisms Increase Lung Cancer Risk In A High-Incidence Region Of Spain: A Case Control Study

Pharmacogenetic Testing And Therapeutic Drug Monitoring Are Complementary Tools For Optimal Individualization Of Drug Therapy

Cyp1a1 Gene Polymorphisms Increase Lung Cancer Risk In A High-Incidence Region Of Spain: A Case Control Study

Pharmacogenetic Testing And Therapeutic Drug Monitoring Are Complementary Tools For Optimal Individualization Of Drug Therapy

Gst Polymorphisms Interact With Dietary Factors To Modulate Lung Cancer Risk: Study In A High-Incidence Area

Pharmacogenetic Testing And Therapeutic Drug Monitoring Are Complementary Tools For Optimal Individualization Of Drug Therapy

Gst Polymorphisms Interact With Dietary Factors To Modulate Lung Cancer Risk: Study In A High-Incidence Area

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

Gst Polymorphisms Interact With Dietary Factors To Modulate Lung Cancer Risk: Study In A High-Incidence Area

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

In Vivo Evaluation Of Cyp2a6 And Xanthine Oxidase Enzyme Activities In The Serbian Population

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

In Vivo Evaluation Of Cyp2a6 And Xanthine Oxidase Enzyme Activities In The Serbian Population

Terapéutica Y Farmacología Práctica Veterinaria, 2010-2011

In Vivo Evaluation Of Cyp2a6 And Xanthine Oxidase Enzyme Activities In The Serbian Population

Terapéutica Y Farmacología Práctica Veterinaria, 2010-2011

Chronic Haemolytic Anaemia Because Of Pyruvate Kinase (Pk) Deficiency In A Child Heterozygous For Haemoglobin S And No Clinical Features Of Sickle Cell Disease

Terapéutica Y Farmacología Práctica Veterinaria, 2010-2011

Chronic Haemolytic Anaemia Because Of Pyruvate Kinase (Pk) Deficiency In A Child Heterozygous For Haemoglobin S And No Clinical Features Of Sickle Cell Disease

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population.

Chronic Haemolytic Anaemia Because Of Pyruvate Kinase (Pk) Deficiency In A Child Heterozygous For Haemoglobin S And No Clinical Features Of Sickle Cell Disease

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population.

Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico

N-Acetyltransferase-2 (Nat2) Gene Polymorphisms And Enzyme Activity In Serbs: Unprecedented High Prevalence Of Rapid Acetylators In A White Population.

Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico

Polymorphisms In Methotrexate Pathways: What Is Clinically Relevant, What Is Not, And What Is Promising

Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico

Polymorphisms In Methotrexate Pathways: What Is Clinically Relevant, What Is Not, And What Is Promising

Promoting Appropriate Drug Use Through The Application Of The Spanish Drug-Related Problem Classification System In The Primary Care Setting

Polymorphisms In Methotrexate Pathways: What Is Clinically Relevant, What Is Not, And What Is Promising

Promoting Appropriate Drug Use Through The Application Of The Spanish Drug-Related Problem Classification System In The Primary Care Setting

Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment

Promoting Appropriate Drug Use Through The Application Of The Spanish Drug-Related Problem Classification System In The Primary Care Setting

Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment

Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)

Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment

Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)

Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome

Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)

Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome

A Common Polymorphism In The Bile Acid Receptor Farnesoid X Receptor Is Associated With Decreased Hepatic Target Gene Expression

Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome

A Common Polymorphism In The Bile Acid Receptor Farnesoid X Receptor Is Associated With Decreased Hepatic Target Gene Expression

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

A Common Polymorphism In The Bile Acid Receptor Farnesoid X Receptor Is Associated With Decreased Hepatic Target Gene Expression

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

Retinal Toxic Reactions Following Photopheresis

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

Retinal Toxic Reactions Following Photopheresis

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

Retinal Toxic Reactions Following Photopheresis

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.

Infection Caused By Fusarium Species In Non-Neutropenic Oncological Patients [4]

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

Infection Caused By Fusarium Species In Non-Neutropenic Oncological Patients [4]

Resolution Of Disseminated Fusariosis In A Child With Acute Leukemia Treated With Combined Antifungal Therapy: A Case Report

Infection Caused By Fusarium Species In Non-Neutropenic Oncological Patients [4]

Resolution Of Disseminated Fusariosis In A Child With Acute Leukemia Treated With Combined Antifungal Therapy: A Case Report

Observation Of The Effects Of Dust Particles On Plasma Fluctuation Spectra.

Resolution Of Disseminated Fusariosis In A Child With Acute Leukemia Treated With Combined Antifungal Therapy: A Case Report

Observation Of The Effects Of Dust Particles On Plasma Fluctuation Spectra.

Adinosine Triphosphate-Binding Cassette B1 (Abcb1) (Multidrug Resistance 1) G2677t/a Gene Polymorphism Is Associated With High Risk Of Lung Cancer

Observation Of The Effects Of Dust Particles On Plasma Fluctuation Spectra.

Adinosine Triphosphate-Binding Cassette B1 (Abcb1) (Multidrug Resistance 1) G2677t/a Gene Polymorphism Is Associated With High Risk Of Lung Cancer

The Effect Of Cyp2j2, Cyp3a4, Cyp3a5 And The Mdr1 C3435t Polymorphisms And Gender On The Urinary Excretion Of The Metabolites Of The H1-Receptor Antihistamine Ebastine: A Pilot Study

Adinosine Triphosphate-Binding Cassette B1 (Abcb1) (Multidrug Resistance 1) G2677t/a Gene Polymorphism Is Associated With High Risk Of Lung Cancer

The Effect Of Cyp2j2, Cyp3a4, Cyp3a5 And The Mdr1 C3435t Polymorphisms And Gender On The Urinary Excretion Of The Metabolites Of The H1-Receptor Antihistamine Ebastine: A Pilot Study

Pharmacogenetics Of Cytochrome P450 (Cyp) 1a2 And Variability In Psychotropic Drug Response

The Effect Of Cyp2j2, Cyp3a4, Cyp3a5 And The Mdr1 C3435t Polymorphisms And Gender On The Urinary Excretion Of The Metabolites Of The H1-Receptor Antihistamine Ebastine: A Pilot Study

Pharmacogenetics Of Cytochrome P450 (Cyp) 1a2 And Variability In Psychotropic Drug Response

Early Mitochondrial Dysfunction In An Infant With Alexander Disease

Pharmacogenetics Of Cytochrome P450 (Cyp) 1a2 And Variability In Psychotropic Drug Response

Early Mitochondrial Dysfunction In An Infant With Alexander Disease

Differences In Cyp3a5*3 Genotype Distribution And Combinations With Other Polymorphisms Between Spaniards And Other Caucasian Populations

Early Mitochondrial Dysfunction In An Infant With Alexander Disease

Differences In Cyp3a5*3 Genotype Distribution And Combinations With Other Polymorphisms Between Spaniards And Other Caucasian Populations

Evaluation Of A Drug-Drug Interaction Alert Structure Through The Retrospective Analysis Of Statins-Macrolides Co-Prescriptions

Differences In Cyp3a5*3 Genotype Distribution And Combinations With Other Polymorphisms Between Spaniards And Other Caucasian Populations

Evaluation Of A Drug-Drug Interaction Alert Structure Through The Retrospective Analysis Of Statins-Macrolides Co-Prescriptions

Polymorphisms In Human Organic Anion-Transporting Polypeptide 1a2 (Oatp1a2): Implications For Altered Drug Disposition And Central Nervous System Drug Entry

Evaluation Of A Drug-Drug Interaction Alert Structure Through The Retrospective Analysis Of Statins-Macrolides Co-Prescriptions

Polymorphisms In Human Organic Anion-Transporting Polypeptide 1a2 (Oatp1a2): Implications For Altered Drug Disposition And Central Nervous System Drug Entry

Potential Role Of Cerebral Cytochrome P450 In Clinical Pharmacokinetics: Modulation By Endogenous Compounds

Polymorphisms In Human Organic Anion-Transporting Polypeptide 1a2 (Oatp1a2): Implications For Altered Drug Disposition And Central Nervous System Drug Entry

Potential Role Of Cerebral Cytochrome P450 In Clinical Pharmacokinetics: Modulation By Endogenous Compounds

Using A Computerized Drug Prescription Screening System To Trace Drug Interactions In An Outpatient Setting

Potential Role Of Cerebral Cytochrome P450 In Clinical Pharmacokinetics: Modulation By Endogenous Compounds

Using A Computerized Drug Prescription Screening System To Trace Drug Interactions In An Outpatient Setting

Early Detection Of Drug Interactions Utilizing A Computerized Drug Prescription Handling System - Focus On Cerivastatin-Gemfibrozil

Using A Computerized Drug Prescription Screening System To Trace Drug Interactions In An Outpatient Setting

Early Detection Of Drug Interactions Utilizing A Computerized Drug Prescription Handling System - Focus On Cerivastatin-Gemfibrozil

Holt-Oram Syndrome [4]

Early Detection Of Drug Interactions Utilizing A Computerized Drug Prescription Handling System - Focus On Cerivastatin-Gemfibrozil

Holt-Oram Syndrome [4]

Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association

Holt-Oram Syndrome [4]

Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association

Thrombocytopenia And Fatality Associated With Olanzapine.

Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association

Thrombocytopenia And Fatality Associated With Olanzapine.

Thrombocytopenia And Fatality Associated With Olanzapine [2]

Thrombocytopenia And Fatality Associated With Olanzapine.

Thrombocytopenia And Fatality Associated With Olanzapine [2]

Zellweger Syndrome. Reports On Two New Cases

Thrombocytopenia And Fatality Associated With Olanzapine [2]

Zellweger Syndrome. Reports On Two New Cases

Fotoféresis: Nueva Terapia Inmunomoduladora Para Enfermedades Mediadas Por Linfocitos T.

Zellweger Syndrome. Reports On Two New Cases

Fotoféresis: Nueva Terapia Inmunomoduladora Para Enfermedades Mediadas Por Linfocitos T.

Photopheresis: New Immunomodulatory Therapy For T-Lymphocyte Mediated Diseases

Fotoféresis: Nueva Terapia Inmunomoduladora Para Enfermedades Mediadas Por Linfocitos T.

Photopheresis: New Immunomodulatory Therapy For T-Lymphocyte Mediated Diseases

Applicability Of An Assay For Routine Monitoring Of Highly Variable Concentrations Of Olanzapine Based On Hplc With Mass Spectrometric Detection

Photopheresis: New Immunomodulatory Therapy For T-Lymphocyte Mediated Diseases

Applicability Of An Assay For Routine Monitoring Of Highly Variable Concentrations Of Olanzapine Based On Hplc With Mass Spectrometric Detection

Genotype-Phenotype Associations For Common Cyp3a4 And Cyp3a5 Variants In The Basal And Induced Metabolism Of Midazolam In European- And African-American Men And Women

Applicability Of An Assay For Routine Monitoring Of Highly Variable Concentrations Of Olanzapine Based On Hplc With Mass Spectrometric Detection

Genotype-Phenotype Associations For Common Cyp3a4 And Cyp3a5 Variants In The Basal And Induced Metabolism Of Midazolam In European- And African-American Men And Women

Role Of The Smoking-Induced Cytochrome P450 (Cyp)1a2 And Polymorphic Cyp2d6 In Steady-State Concentration Of Olanzapine

Genotype-Phenotype Associations For Common Cyp3a4 And Cyp3a5 Variants In The Basal And Induced Metabolism Of Midazolam In European- And African-American Men And Women

Role Of The Smoking-Induced Cytochrome P450 (Cyp)1a2 And Polymorphic Cyp2d6 In Steady-State Concentration Of Olanzapine

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

Role Of The Smoking-Induced Cytochrome P450 (Cyp)1a2 And Polymorphic Cyp2d6 In Steady-State Concentration Of Olanzapine

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

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

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

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

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

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

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

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

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

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

Aplastic Anemia During Treatment With Albendazole [8]

Tryptamine: A Possible Endogenous Substrate For Cyp2d6

Aplastic Anemia During Treatment With Albendazole [8]

Changes In Platelet Count: A Primary Or Secondary Effect Of Rhu-Epo Therapy?

Aplastic Anemia During Treatment With Albendazole [8]

Changes In Platelet Count: A Primary Or Secondary Effect Of Rhu-Epo Therapy?

Assessment Of Iron Status By Erythrocyte Ferritin In Uremic Patients With Or Without Recombinant Human Erythropoietin Therapy

Changes In Platelet Count: A Primary Or Secondary Effect Of Rhu-Epo Therapy?

Assessment Of Iron Status By Erythrocyte Ferritin In Uremic Patients With Or Without Recombinant Human Erythropoietin Therapy

Tamaño De La Fontanela En El Recién Nacido Normal. Relación Con Parámetros Antropométricos Y Bioquímicos

Assessment Of Iron Status By Erythrocyte Ferritin In Uremic Patients With Or Without Recombinant Human Erythropoietin Therapy

Tamaño De La Fontanela En El Recién Nacido Normal. Relación Con Parámetros Antropométricos Y Bioquímicos

Prognostic Significance Of Mutation Type And Chromosome Fragility In Fanconi Anemia