A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

por Balta, Burhan, Erdoğan, Murat, Kiraz, Aslıhan, Korkmaz, Serdal, Ağadayı, Alperen
Publicado 2019

Investigation of the relationship between inherited thrombophilia and novel coronavirus pneumonia

por Kiraz, Aslihan, Guzeldag, Seda, Eren, Esma, Goksu, Musa, Bayram, Arslan
Publicado 2021

Osteopontin as an early predictor of atherosclerosis in attack-free Familial Mediterranean fever patients

por Baspinar, Osman, Kocer, Derya, Kiraz, Aslihan, Tokmak, Turgut Tursem, Dizdar, Oguzhan Sitki
Publicado 2023

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome.

por Akın, Mustafa Ali, Güneş, Tamer, Akın, Leyla, Çoban, Dilek, Kara Oncu, Sena, Kiraz, Aslıhan, Kurtoğlu, Selim
Publicado 2011

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients

por Dundar, Munis, Kiraz, Aslihan, Emirogullari, Elif Funda, Saatci, Çetin, Taheri, Serpil, Baskol, Mevlut, Polat, Seher, Özkul, Yusuf
Publicado 2012

The Genetic Analysis of Cystic Fibrosis Patients with Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

por Erdoğan, Murat, Köse, Mehmet, Pekcan, Sevgi, Hangül, Melih, Balta, Burhan, Kiraz, Aslıhan, Akıncı Gönen, Gizem, Gül Zamani, Ayşe, Selman Yıldırım, Mahmut, Ramaslı Gürsoy, Tuğba, Ezgu, Fatih, Şişmanlar Eyüpoğlu, Tuğba, Tana Aslan, Ayse
Publicado 2021