Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience
Berkay Saraymen, Sabahattin Muhtaroğlu, Mustafa Yavuz Köker, Nazan Sarper et autres
Background/aim: Glanzmann thrombasthenia (GT) is a rare autosomal recessively inherited bleeding disorder characterized by the quantitative (type 1 and type 2) or qualitative (type 3) deficiency in platelet membrane glycoprotein (GP) IIb/IIIa (CD41a/CD61) fibrinogen receptors. In type 1, 2, and 3, CD41a/CD61 …
tr (code pays fourni par la source)
10 citations
TURKISH JOURNAL OF MEDICAL SCIENCES