Atıf İçin Kopyala
Genc A., GÜNAŞTI S., TULİ A., ÇÜRÜK M. A., UZUN S.
POSTEPY DERMATOLOGII I ALERGOLOGII, cilt.29, sa.1, ss.25-29, 2012 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
29
Sayı:
1
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Basım Tarihi:
2012
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Dergi Adı:
POSTEPY DERMATOLOGII I ALERGOLOGII
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.25-29
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Anahtar Kelimeler:
thiopurine S-methyltransferase, azathioprine, pemphigus vulgaris, pharmacogenetic, INFLAMMATORY-BOWEL-DISEASE, AZATHIOPRINE THERAPY, CROHNS-DISEASE, PHARMACOGENETICS, GENOTYPE, PHENOTYPE, TPMT, POPULATION, FREQUENCY, LEUKEMIA
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Akdeniz Üniversitesi Adresli:
Evet
Özet
Introduction: Thiopurine S-methyltransferase (TPMT) genotypes or phenotypes are important as a predictive factor for thiopurine-induced toxicity. Individuals who are TPMT deficient or have intermediate TPMT activity are at risk of developing myelosuppression and life-threatening leucopenia when treated with standard doses of thiopurines; thus, pretreatment identification of these individuals is very important.