PUBLICACIÓN

Central nervous system chemotoxicity during treatment of pediatric acute lymphoblastic leukemia/lymphoma

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Vagace J.M., de la Maya M.D., Caceres-Marzal C., Gonzalez de Murillo S., Gervasini G.

2012 Critical Reviews in Oncology/Hematology

Geriatrics and Gerontology (Q1), Hematology (Q1), Oncology (Q1)

JCR: 4.637

SJR: 1.908

CITAS

50

DOI

10.1016/j.critrevonc.2012.04.003

EID

2-s2.0-84867842532

ISSN

1040-8428

EISSN

1879-0461

BIBTEX

@article{PMID:22578745, title = {Central nervous system chemotoxicity during treatment of pediatric acute lymphoblastic leukemia/lymphoma.}, author = {Vagace JM and de la Maya MD and Caceres-Marzal C and Gonzalez de Murillo S and Gervasini G}, doi = {10.1016/j.critrevonc.2012.04.003}, journal = {Critical reviews in oncology/hematology}, month = {11}, year = {2012} }

AUTORES DE LA UEX

Guillermo Gervasini Rodríguez
José Manuel Vagace Valero
Cristina Cáceres Marzal

OTRAS PUBLICACIONES DE INTERÉS

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