Factor V Leiden and prothrombin gene G20210A mutations in ocular Behcet disease

ŞERMET F., Atmaca L., KARABULUT H. G., Sayin D.

ACTA OPHTHALMOLOGICA SCANDINAVICA, cilt.81, sa.3, ss.283-285, 2003 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 81 Sayı: 3
  • Basım Tarihi: 2003
  • Doi Numarası: 10.1034/j.1600-0420.2003.00068.x
  • Dergi Adı: ACTA OPHTHALMOLOGICA SCANDINAVICA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.283-285
  • Anahtar Kelimeler: Behcet's disease, procoagulant factors, factor V Leiden mutation, prothrombin G20210A-mutation, vascular occlusion, COAGULATION-FACTOR-V, ACTIVATED PROTEIN-C, PERIPHERAL RETINAL NEOVASCULARIZATION, VENOUS THROMBOSIS, TURKISH POPULATION, VEIN OCCLUSION, RESISTANCE, RISK
  • Ankara Üniversitesi Adresli: Evet

Özet

Purpose: To investigate genetic prothrombotic factors (factor V Leiden and prothrombin gene G20210A mutations) and their relation with retinal vascular occlusions in ocular Behcet disease.