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Lista de obras de José Agundez

7th drug hypersensitivity meeting: part one.

artículo científico publicado en 2016

A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels

artículo científico publicado en 2016

A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor

artículo científico publicado en 2016

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.

artículo científico publicado en 2011

Acetylator status and N-acetyltransferase 2 gene polymorphisms; phenotype-genotype correlation with the sulfamethazine test

artículo científico publicado en 2011

Acquired resistance to the anticancer drug paclitaxel is associated with induction of cytochrome P450 2C8.

artículo científico publicado en 2006

Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease

artículo científico publicado en 2016

Alcohol consumption and risk for Parkinson's disease: a systematic review and meta-analysis

scientific article published on 28 August 2018

Alcohol dehydrogenase 2 genotype and allelic variants are not associated with the risk for essential tremor

artículo científico publicado en 2007

Alcohol dehydrogenase 2 genotype and risk for migraine.

artículo científico publicado en 2009

Allergic Reactions to Metamizole: Immediate and Delayed Responses

artículo científico publicado en 2016

Aminopyrine metabolism in man: the acetylation of aminoantipyrine cosegregates with acetylation of caffeine

scientific article published on 01 February 1995

An Update on the Neurochemistry of Essential Tremor

scientific article published on 01 January 2020

An Update on the Role of Nitric Oxide in the Neurodegenerative Processes of Parkinson's Disease

artículo científico publicado en 2016

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease

artículo científico publicado en 2014

An update on the pharmacogenomics of NSAID metabolism and the risk of gastrointestinal bleeding

scientific article published on 29 March 2020

Analysis of a non-synonymous single nucleotide polymorphism of the human diamine oxidase gene (ref. SNP ID: rs1049793) in patients with Crohn's disease

article

Analysis of midazolam and metabolites in plasma by high-performance liquid chromatography: probe of CYP3A.

artículo científico publicado en 1998

Analysis of the Functional Polymorphism in the Cytochrome P450 CYP2C8 Gene rs11572080 with Regard to Colorectal Cancer Risk.

artículo científico publicado en 2012

Anti-Inflammatory Effects of Amantadine and Memantine: Possible Therapeutics for the Treatment of Covid-19?

artículo científico publicado en 2020

Arylamine N-acetyltransferase 2 genotypes in a Mexican population

artículo científico publicado en 2012

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.

artículo científico publicado en 2015

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.

artículo científico publicado en 2017

Association Study Among Candidate Genetic Polymorphisms and Chemotherapy-Related Severe Toxicity in Testicular Cancer Patients

article

Association between endothelial nitric oxide synthase (NOS3) rs2070744 and the risk for migraine

scientific article published on 03 December 2019

Association between restless legs syndrome and other movement disorders

artículo científico publicado en 2019

Association between the missense alcohol dehydrogenase rs1229984T variant with the risk for Parkinson's disease in women

scientific article published on 27 November 2018

Association between the oxidative polymorphism and early onset of Parkinson's disease

artículo científico publicado en 1995

Association of CYP2C9 genotypes leading to high enzyme activity and colorectal cancer risk.

artículo científico publicado en 2001

Asthma and Rhinitis Induced by Selective Immediate Reactions to Paracetamol and Non-steroidal Anti-inflammatory Drugs in Aspirin Tolerant Subjects.

artículo científico publicado en 2016

COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis

artículo científico publicado en 2014

CYP2A6 gene polymorphism and risk of liver cancer and cirrhosis

artículo científico publicado en 1997

CYP2C19 polymorphism and risk for essential tremor

artículo científico publicado en 2006

CYP2D6 genes and risk of liver cancer

artículo científico publicado en 1995

CYP2D6 genotypes in Spanish women with breast cancer

article

CYP2D6 polymorphism is not associated with essential tremor

scientific article published on 01 January 1997

CYP2D6, NAT2 and CYP2E1 genetic polymorphisms in nonagenarians

artículo científico publicado en 1997

CYP2W1 variant alleles in Caucasians and association of the CYP2W1 G541A (Ala181Thr) polymorphism with increased colorectal cancer risk

artículo científico publicado en 2010

CYP3A4 variant alleles in white individuals with low CYP3A4 enzyme activity

artículo científico publicado en 2002

Caffeine demethylase activity in human and Dark Agouti rat liver microsomes. Comparison with aminopyrine N-demethylase activity

scientific article published on 01 May 1992

Cerebrospinal fluid biochemical studies in patients with Parkinson's disease: toward a potential search for biomarkers for this disease.

artículo científico publicado en 2014

Changes at the CYP2C locus and disruption of CYP2C8/9 linkage disequilibrium in patients with essential tremor

artículo científico publicado en 2007

Characteristics of subjects experiencing hypersensitivity to non-steroidal anti-inflammatory drugs: patterns of response

artículo científico publicado en 2010

Clarifying haplotype ambiguity of NAT2 in multi-national cohorts.

artículo científico publicado en 2013

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C9 and Nonsteroidal Anti-inflammatory Drugs

scientific article published on 19 March 2020

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP2C19 and Voriconazole Therapy.

artículo científico publicado en 2016

Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 genotype and use of ondansetron and tropisetron

artículo científico publicado en 2016

Clinical pharmacogenomic testing of KRAS, BRAF and EGFR mutations by high resolution melting analysis and ultra-deep pyrosequencing

artículo científico publicado en 2011

Clinical practice guidelines for translating pharmacogenomic knowledge to bedside. Focus on anticancer drugs

artículo científico publicado en 2014

Copy number variation in ALOX5 and PTGER1 is associated with NSAIDs-induced urticaria and/or angioedema

artículo científico publicado en 2016

Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor

scientific article published on 24 January 2020

Cytochrome P450 CYP2B6 genotypes and haplotypes in a Colombian population

artículo científico publicado en 2011

Cytochrome P450 CYP2C9 Polymorphism and NSAID-Related Acute Gastrointestinal Bleeding

scientific article published on 01 December 2007

Cytochrome P450 gene polymorphism and cancer

artículo científico publicado en 2004

Debrisoquin oxidation genotype and susceptibility to lung cancer

artículo científico publicado en 1994

Debrisoquine polymorphism: mechanism for very rapid oxidative phenotype

artículo científico publicado en 1993

Delta-amino-levulinic acid dehydratase gene and essential tremor

artículo científico publicado en 2017

Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing ⬇️

artículo científico publicado el 16 de marzo de 2012

Determination of aminopyrine and dipyrone metabolites in urine

scientific article published on 01 February 1996

Determination of aminopyrine, dipyrone and its metabolites in urine by high-performance liquid chromatography

scientific article published on 01 June 1994

Detoxifying Enzymes at the Cross-Roads of Inflammation, Oxidative Stress, and Drug Hypersensitivity: Role of Glutathione Transferase P1-1 and Aldose Reductase

artículo científico publicado en 2016

Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine

artículo científico publicado en 2015

Dopamine receptor 3 (DRD3) polymorphism and risk for migraine

artículo científico publicado en 2010

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

artículo científico publicado en 2013

Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.

artículo científico publicado en 2009

Drug and xenobiotic biotransformation in the blood-brain barrier: a neglected issue. ⬇️

artículo científico publicado en 2014

Drug metabolism and hypersensitivity reactions to drugs

artículo científico

Editorial [Hot Topic: N-Acetyltransferases: Lessons Learned from Eighty Years of Research (Guest Editor: Jose A.G. Agundez) ]

artículo científico publicado en 2008

Editorial on Cerebral endothelial and glial cells are more than bricks in the Great Wall of the brain: insights into the way the blood-brain barrier actually works (celebrating the centenary of Goldman's experiments).

artículo científico publicado en 2015

Editorial: Biomarkers in Drug Hypersensitivity.

artículo científico publicado en 2017

Editorial: clinical use of biomarkers in drug metabolism and adverse drug reactions

artículo científico publicado en 2014

Effect of common NAT2 variant alleles in the acetylation of the major clonazepam metabolite, 7-aminoclonazepam

artículo científico publicado en 2007

Effect of neurotransmitters on NADPH-cytochrome P450 reductase in vitro activity

artículo científico publicado en 2007

Evaluation of immediate allergic reactions to dipyrone using dipyrone metabolites in basophil activation test

artículo científico publicado en 2014

Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: implications for drug therapy

artículo científico publicado en 2002

FCERI and Histamine Metabolism Gene Variability in Selective Responders to NSAIDS

artículo científico publicado en 2016

Farmacogenómica clínica de CYP2C8 y CYP2C9: conceptos generales y aplicación al uso de AINE

scientific article published on 01 July 2006

Frequencies of 23 functionally significant variant alleles related with metabolism of antineoplastic drugs in the chilean population: comparison with caucasian and asian populations.

artículo científico publicado en 2012

Frequency of CYP2D6 allelic variants in multiple sclerosis

artículo científico publicado en 1995

Functionally active duplications of the CYP2D6 gene are more prevalent among larynx and lung cancer patients.

artículo científico publicado en 2001

Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in Europeans

artículo científico publicado en 2013

GC Gene Polymorphism and Unbound Serum Retinol-Binding Protein 4 Are Related to the Risk of Insulin Resistance in Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study.

artículo científico publicado en 2016

GSTT1 and GSTM1 null genotypes may facilitate hepatitis C virus infection becoming chronic

artículo científico publicado en 2007

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.

artículo científico

Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor

artículo científico publicado en 2010

Gamma-aminobutyric acid (GABA) receptors GABRA4, GABRE, and GABRQ gene polymorphisms and risk for migraine

artículo científico publicado en 2018

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.

artículo científico publicado en 2018

Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor

artículo científico publicado en 2011

Gender and functional CYP2C and NAT2 polymorphisms determine the metabolic profile of metamizole

artículo científico publicado en 2014

Gene variants and haplotypes modifying transcription factor binding sites in the human cyclooxygenase 1 and 2 (PTGS1 and PTGS2) genes.

artículo científico publicado en 2014

Genetic analysis of the NAT2 and CYP2D6 polymorphisms in white patients with non-insulin-dependent diabetes mellitus

artículo científico publicado en 1996

Genetic basis for differences in debrisoquin polymorphism between a Spanish and other white populations

scientific article published on 01 April 1994

Genetic determinants of metamizole metabolism modify the risk of developing anaphylaxis

artículo científico publicado en 2015

Genetic predisposition to acute gastrointestinal bleeding after NSAIDs use

artículo científico publicado en 2004

Genetic variability of histamine receptors in patients with Parkinson's disease.

artículo científico publicado en 2008

Genetic variability of human diamine oxidase: occurrence of three nonsynonymous polymorphisms and study of their effect on serum enzyme activity

artículo científico publicado en 2007

Genetic variants of the arachidonic acid pathway in non-steroidal anti-inflammatory drug-induced acute urticaria

artículo científico publicado en 2012

Genetically based impairment in CYP2C8- and CYP2C9-dependent NSAID metabolism as a risk factor for gastrointestinal bleeding: Is a combination of pharmacogenomics and metabolomics required to improve personalized medicine?

artículo científico publicado en 2009

Genetics of restless legs syndrome: An update

artículo científico publicado en 2017

Genome-wide association study raised biomarker SLC1A2 rs3794087 and essential tremor: is it too early to say?

artículo científico publicado en 2013

Genomic and pharmacogenomic biomarkers of Parkinson's disease.

artículo científico publicado en 2014

Glutathione S-transferase GSTT1 and GSTM1 allozymes: beyond null alleles

artículo científico publicado en 2008

Glutathione S-transferase M1 and T1 genetic polymorphisms are not related to the risk of hepatocellular carcinoma: a study in the Spanish population

artículo científico publicado en 2005

Glutathione S-transferase m1 and t1 null genotypes increase susceptibility to idiosyncratic drug-induced liver injury.

artículo científico publicado en 2008

Glutathione S-transferases mu 1, theta 1, pi 1, alpha 1 and mu 3 genetic polymorphisms and the risk of colorectal and gastric cancers in humans.

artículo científico publicado en 2006

Glutathione-S-transferase P1 polymorphism and risk for essential tremor

artículo científico publicado en 2008

GlutathioneS-transferases π1, α1 and µ3 genetic polymorphisms and the risk of hepatocellular carcinoma in humans

scientific article published on 01 August 2007

H1-MAPT and the risk for familial essential tremor

artículo científico publicado en 2012

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor.

artículo científico publicado en 2015

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

artículo científico publicado en 2016

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.

artículo científico publicado en 2015

Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia

artículo científico publicado en 2013

High frequency of mutations related to impaired CYP2C9 metabolism in a Caucasian population

scientific article published on 01 April 2001

High resolution mapping and mutation analyses of candidate genes in the urofacial syndrome (UFS) critical region

artículo científico publicado en 2003

High-resolution melting analysis of the common c.1905+1G>A mutation causing dihydropyrimidine dehydrogenase deficiency and lethal 5-fluorouracil toxicity.

artículo científico publicado en 2012

Histamine pharmacogenomics.

scientific article published on May 2009

Histamine-N-methyl transferase polymorphism and risk for migraine

artículo científico publicado en 2008

Hypersensitivity reactions to non-steroidal anti-inflammatory drugs.

artículo científico publicado en 2009

Hypersensitivity reactions to nonsteroidal anti-inflammatory drugs: an update on pharmacogenetics studies

artículo científico publicado en 2018

Identification and characterisation of novel polymorphisms in the CYP2A locus: implications for nicotine metabolism

artículo científico publicado en 1999

Identification and prevalence study of 17 allelic variants of the human NAT2 gene in a white population

artículo científico publicado en 1996

Identification of Novel Biomarkers for Drug Hypersensitivity After Sequencing of the Promoter Area in 16 Genes of the Vitamin D Pathway and the High-Affinity IgE Receptor

scientific article published on 25 June 2019

Identification of subtypes of CYP2D gene rearrangements among carriers of CYP2D6 gene deletion and duplication

artículo científico publicado en 2005

Immediate hypersensitivity reactions to ibuprofen and other arylpropionic acid derivatives

artículo científico publicado en 2016

Immediate reactions to more than one NSAID must not be considered as cross-hypersensitivity unless asa tolerance is verified

artículo científico publicado en 2016

Impairment of rapid repetitive finger movements and visual reaction time in patients with essential tremor

artículo científico publicado en 2009

Improved analytical sensitivity reveals the occurrence of gender-related variability in diamine oxidase enzyme activity in healthy individuals

scientific article published on 11 August 2007

Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process

artículo científico publicado en 2014

Increased frequency of rapid acetylator genotypes in patients with brain astrocytoma and meningioma

artículo científico publicado en 2006

Increased risk for hepatocellular carcinoma in NAT2-slow acetylators and CYP2D6-rapid metabolizers

scientific article published on 01 December 1996

Influence of age and gender in motor performance in healthy subjects

artículo científico publicado en 2010

Influence of cytochrome P450 CYP2C9 genotypes in lung cancer risk

artículo científico publicado en 2002

Influence of genetic admixture on polymorphisms of drug-metabolizing enzymes: analyses of mutations on NAT2 and C gamma P2E1 genes in a mixed Hispanic population

artículo científico publicado en 1998

Influence of vitamin D-related gene polymorphisms (CYP27B and VDR) on the response to interferon/ribavirin therapy in chronic hepatitis C

artículo científico publicado en 2013

Interaction of CYP2C8 and CYP2C9 genotypes modifies the risk for nonsteroidal anti-inflammatory drugs-related acute gastrointestinal bleeding

artículo científico publicado en 2008

Interethnic and intraethnic variability of CYP2C8 and CYP2C9 polymorphisms in healthy individuals

artículo científico publicado en 2006

Interindividual variability in ibuprofen pharmacokinetics is related to interaction of cytochrome P450 2C8 and 2C9 amino acid polymorphisms

artículo científico publicado en 2004

LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.

artículo científico publicado en 2012

LINGO1 gene analysis in Parkinson's disease phenotypes.

artículo científico publicado en 2011

LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson’s disease: Results of a meta-analysis

article

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

artículo científico publicado en 2013

Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor.

artículo científico publicado en 2010

Leflunomide-induced acute hepatitis

artículo científico publicado en 2004

Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

artículo científico publicado en 2010

Loss-of-function mutations in HPSE2 cause the autosomal recessive urofacial syndrome

scientific journal article

Lung cancer and mutations at the polymorphic NAT2 gene locus

scientific article published on 01 August 1995

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

artículo científico publicado en 2013

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.

artículo científico publicado en 2012

Metabolic considerations of drugs in the treatment of allergic diseases.

artículo científico

Metabolism of aminopyrine and derivatives in man: in vivo study of monomorphic and polymorphic metabolic pathways

scientific article published on 01 April 1995

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo.

artículo científico publicado en 2018

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

artículo científico publicado en 2015

Mitochondrial superoxide dismutase and glutathione peroxidase in idiosyncratic drug-induced liver injury.

artículo científico publicado en 2010

Modulation of CYP1A2 enzyme activity by indoleamines: inhibition by serotonin and tryptamine

artículo científico publicado en 1998

Modulation of GSTP1-1 oligomerization by electrophilic inflammatory mediators and reactive drugs.

artículo científico publicado en 2013

Modulation of midazolam 1-hydroxylation activity in vitro by neurotransmitters and precursors

artículo científico publicado en 2000

Molecular Interactions and Implications of Aldose Reductase Inhibition by PGA1 and Clinically Used Prostaglandins.

artículo científico publicado en 2015

Molecular analysis of the arylamine N-acetyltransferase polymorphism in a Spanish population

scientific article published on 01 August 1994

Molecular heterogeneity at the CYP2D gene locus in Nicaraguans: impact of gene-flow from Europe ⬇️

artículo científico publicado el 1 de agosto de 1997

Motor performance in patients with restless legs syndrome.

artículo científico publicado en 2009

N-acetyltransferase 2 polymorphism is not related to the risk of advanced alcoholic liver disease

artículo científico publicado en 2002

N-acetyltransferase 2 polymorphisms and risk of anti-tuberculosis drug-induced hepatotoxicity in Caucasians

artículo científico publicado en 2011

N-acetyltransferase 2 single-nucleotide polymorphisms and risk of gastric carcinoma

scientific article published on 17 April 2002

NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis

artículo científico publicado en 2016

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

artículo científico publicado en 2014

NSAIDs-hypersensitivity often induces a blended reaction pattern involving multiple organs

artículo científico publicado en 2018

Neurochemical features of idiopathic restless legs syndrome

artículo científico publicado en 2019

Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine

artículo científico publicado en 2015

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

artículo científico publicado en 2014

New Advances in the Study of IgE Drug Recognition.

artículo científico publicado en 2016

Next-Generation Sequencing of Genes Reveals an Increased Frequency of Non-synonymous Variants Among Patients With NSAID-Induced Liver Injury

article

No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population

artículo científico publicado en 2013

Nonsynonymous polymorphisms of histamine-metabolising enzymes in patients with Parkinson's disease

artículo científico publicado en 2007

Oxidative stress in skin fibroblasts cultures from patients with Parkinson's disease

artículo científico publicado en 2010

PITX3 and risk for Parkinson's disease: a systematic review and meta-analysis.

artículo científico

Paraoxonase 1 (PON1) polymorphisms and risk for essential tremor

artículo científico publicado en 2009

Paraoxonase 1 (PON1) polymorphisms and risk for migraine

scientific article published on 21 April 2010

Paraoxonase 1 Polymorphisms Are Not Related with the Risk for Multiple Sclerosis

artículo científico publicado en 2009

Perception of the usefulness of drug/gene pairs and barriers for pharmacogenomics in Latin America.

artículo científico publicado en 2014

Perspective on the use of genomic biomarkers in the clinical setting

artículo científico publicado en 2014

PharmVar GeneFocus: CYP2D6

artículo científico publicado en 2019

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

artículo científico publicado en 2019

Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.

artículo científico publicado en 2015

Pharmacogenomics in aspirin intolerance.

artículo científico publicado en 2009

Pharmacogenomics of Prostaglandin and Leukotriene Receptors

artículo científico publicado en 2016

Pharmacogenomics of cyclooxygenases

artículo científico

Pharmacogenomics testing for type B adverse drug reactions to anti-infective drugs: the example of hypersensitivity to abacavir

artículo científico publicado en 2014

Pharmacokinetic Interaction of Fluvoxamine and Thioridazine in Schizophrenic Patients

artículo científico publicado en 1999

Polymorphic drug metabolism in anaesthesia.

artículo científico publicado en 2009

Polymorphism of the TLR4 gene reduces the risk of hepatitis C virus-induced hepatocellular carcinoma

artículo científico publicado en 2012

Polymorphisms in the transforming growth factor-beta gene (TGF-beta) and the risk of advanced alcoholic liver disease

artículo científico publicado en 2005

Polymorphisms of histamine-metabolizing enzymes and clinical manifestations of asthma and allergic rhinitis

artículo científico publicado en 2007

Polymorphisms of human N-acetyltransferases and cancer risk

artículo científico publicado en 2008

Polymorphisms of the glutathione S-transferases mu-1 (GSTM1) and theta-1 (GSTT1) and the risk of advanced alcoholic liver disease

artículo científico publicado en 2005

Possible implications of doxycycline-rifampin interaction for treatment of brucellosis

artículo científico publicado en 1994

Predicting response to therapy in chronic hepatitis C: an approach combining interleukin-28B gene polymorphisms and clinical data.

artículo científico publicado en 2012

Prevalence of CYP2D6 gene duplication and its repercussion on the oxidative phenotype in a white population

artículo científico publicado en 1995

Pyrazolones metabolites are relevant for identifying selective anaphylaxis to metamizole

artículo científico publicado en 2016

Recent advances in drug intolerance

artículo científico publicado en 2009

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article

Relation of IL28B gene polymorphism with biochemical and histological features in hepatitis C virus-induced liver disease

artículo científico publicado en 2012

Rsa I polymorphism at the cytochrome P4502E1 locus is not related to the risk of alcohol-related severe liver disease

artículo científico publicado en 1996

SLC1A2 rs3794087 variant and risk for essential tremor: a systematic review and meta-analysis.

artículo científico

SLC1A2 rs3794087 variant and risk for migraine

artículo científico publicado en 2013

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

artículo científico publicado en 2020

Single nucleotide polymorphisms and microsatellite alleles of tumor necrosis factor alpha and interleukin-10 genes and the risk of advanced chronic alcoholic liver disease

artículo científico publicado en 2002

Sleep Disorders in Essential Tremor: Systematic Review and Meta-Analysis

artículo científico publicado en 2020

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

artículo científico publicado en 2014

The Genetics of Drug Hypersensitivity Reactions

artículo científico publicado en 2016

The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs

artículo científico publicado en 2012

The differential effect of NAT2 variant alleles permits refinement in phenotype inference and identifies a very slow acetylation genotype

artículo científico publicado en 2012

The effect of the cytochrome P450 CYP2C8 polymorphism on the disposition of (R)-ibuprofen enantiomer in healthy subjects.

artículo científico publicado en 2005

The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor

artículo científico publicado en 2008

The potential of LINGO-1 as a therapeutic target for essential tremor.

artículo científico publicado en 2015

The potential role of pharmacogenomics and biotransformation in hypersensitivity reactions to paracetamol

artículo científico publicado en 2018

The relationship between Parkinson's disease and essential tremor: review of clinical, epidemiologic, genetic, neuroimaging and neuropathological data, and data on the presence of cardinal signs of parkinsonism in essential tremor

artículo científico publicado en 2012

The role of phase I and II genetic polymorphisms, smoking, alcohol and cancer family history, in the risk of developing testicular cancer

artículo científico publicado en 2019

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

artículo científico publicado en 2013

Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis

artículo científico publicado en 2016

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

artículo científico publicado en 2016

Tryptamine: a possible endogenous substrate for CYP2D6.

artículo científico publicado en 1997

Two common nonsynonymous paraoxonase 1 (PON1) gene polymorphisms and brain astrocytoma and meningioma.

artículo científico publicado en 2010

Update on genetics of essential tremor.

artículo científico

Variability in ethanol biodisposition in whites is modulated by polymorphisms in the ADH1B and ADH1C genes

artículo científico publicado en 2010

Variability in histamine receptor genes HRH1, HRH2 and HRH4 in patients with hypersensitivity to NSAIDs.

artículo científico publicado en 2013

Variability of the L-Histidine decarboxylase gene in allergic rhinitis

artículo científico publicado en 2010

Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs

artículo científico publicado en 2014

Vitamin D deficiency and vitamin D therapy in chronic hepatitis C.

artículo científico publicado en 2013

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis

artículo científico publicado en 2013

[The H63D mutation in the HFE gene is related to the risk of hepatocellular carcinoma]

scientific article published on 01 July 2007

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