Methylenetetrahydrofolate reductase C677T polymorphism in patients with Henoch-Schonlein purpura

Emre S., Sirin A., Ergen A., Bilge I., Sucu A., Yilmaz A., ...Daha Fazla

PEDIATRICS INTERNATIONAL, cilt.53, sa.3, ss.358-362, 2011 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 53 Sayı: 3
  • Basım Tarihi: 2011
  • Doi Numarası: 10.1111/j.1442-200x.2010.03247.x
  • Dergi Adı: PEDIATRICS INTERNATIONAL
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.358-362
  • İstanbul Üniversitesi Adresli: Evet

Özet

Aim: Associations between several vascular diseases such as Kawasaki disease, venous and arterial thromboembolism, cardiovascular disease, diabetic nephropathy, focal segmental glomerulosclerosis and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism have been reported. This is a clinical study designed to investigate the possible effects of MTHFR C677T polymorphism on the development of Henoch-Schonlein purpura (HSP).