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Volumn 44, Issue 11, 2001, Pages 2525-2530
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The C677T mutation in the methylenetetrahydrofolate reductase gene: A genetic risk factor for methotrexate-related elevation of liver enzymes in rheumatoid arthritis patients
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Author keywords
[No Author keywords available]
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Indexed keywords
5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);
ALANINE AMINOTRANSFERASE;
FOLIC ACID;
HOMOCYSTEINE;
LIVER ENZYME;
METHOTREXATE;
PLACEBO;
ADULT;
AGED;
ARTICLE;
CLINICAL TRIAL;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
DOUBLE BLIND PROCEDURE;
DRUG EFFICACY;
FEMALE;
GASTROINTESTINAL SYMPTOM;
GENE MUTATION;
GENETIC RISK;
GENOTYPE;
HAIR LOSS;
HETEROZYGOSITY;
HOMOZYGOSITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
MULTICENTER STUDY;
PRIORITY JOURNAL;
RHEUMATOID ARTHRITIS;
TREATMENT OUTCOME;
ALANINE TRANSAMINASE;
ANTIRHEUMATIC AGENTS;
ARTHRITIS, RHEUMATOID;
DOUBLE-BLIND METHOD;
FEMALE;
FOLIC ACID;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HEMATINICS;
HUMANS;
LIVER;
MALE;
METHOTREXATE;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MIDDLE AGED;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
POINT MUTATION;
SEVERITY OF ILLNESS INDEX;
TREATMENT OUTCOME;
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EID: 0035157121
PISSN: 00043591
EISSN: None
Source Type: Journal
DOI: 10.1002/1529-0131(200111)44:11<2525::AID-ART432>3.0.CO;2-B Document Type: Article |
Times cited : (215)
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References (16)
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