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The Clinical Significance of JAK2V617F Mutation for Philadelphia-Negative Chronic Myeloproliferative Neoplasms in Patients with Splanchic Vein Thrombosis
Hindilerden, Fehmi; Hindilerden, Ipek Yonal; Pinarbasi, Binnur; Hancer, Veysel Sabri; Kaymakoglu, Sabahattin; Kucukkaya, Reyhan Diz; Nalcaci, Meliha (Cig Media Group, Lp, 2019)[No abstract available] -
Glycoprotein Ib-alpha Kozak polymorphism in ischemic stroke
Esen, Fatma Inci; Hancer, Veysel Sabri; Kucukkaya, Reyhan Diz; Yesilot, Nilufer; Coban, Oguzhan; Bahar, Sara; Tuncay, Rezzan (MANEY PUBLISHING, 2012)Background: Recently, a T/C polymorphism in the Kozak sequence of glycoprotein Ib-alpha (GPIb-alpha) gene at position 25 from the initiator ATG codons, has been identified. The presence of -5C allele increases the surface ... -
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
Karacan, Ilker; Kucukkaya, Reyhan Diz; Karakus, Fatma Nur; Solakoglu, Seyhun; Tolun, Aslihan; Hancer, Veysel Sabri; Turanli, Eda Tahir (GALENOS YAYINCILIK, 2019)Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose arid elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutations ...