How do we encounter rare factor deficiencies in children? Single-centre results from Turkey


Tugcu D., Salcioglu Z., Akcay A., Sen H. S., Aydogan G., Akici F., ...Daha Fazla

BLOOD COAGULATION & FIBRINOLYSIS, cilt.26, sa.2, ss.145-151, 2015 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 26 Sayı: 2
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1097/mbc.0000000000000204
  • Dergi Adı: BLOOD COAGULATION & FIBRINOLYSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.145-151
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet

Özet

Background Rare factor deficiencies (RFDs) are autosomal recessively inherited coagulation factor deficiencies encountered at a frequency of between one in 500 000 and one in two million.