Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficiency Anemia

por Demir Yenigürbüz, Fatma, Deveci, Ugur, Tuncez, Ebru
Publicado 2019

Micronuclei frequencies in lymphocytes and cervical cells of women with polycystic ovarian syndrome

por Karataylı, Rengin, Gül Zamani, Ayşe, Gezginç, Kazım, Tuncez, Ebru, Soysal, Sema, Karanfil, Fikriye, Acar, Aynur, Yıldırım, M. Selman
Publicado 2017

High diagnostic yield with algorithmic molecular approach on hereditary neuropathies

por Ceylan, Gülay Güleç, Habiloğlu, Esra, Çavdarlı, Büşranur, Tuncez, Ebru, Bilen, Sule, Köken, Özlem Yayıcı, Gündüz, C. Nur Semerci
Publicado 2023

Are angiotensin converting enzyme (ACE1/ACE2) gene variants associated with the clinical severity of COVID-19 pneumonia? A single-center cohort study

por Baştuğ, Serdal, Çavdarlı, Büşranur, Baştuğ, Aliye, Şencan, İrfan, Tunçez, Ebru, Çakır, Esra Yakışık, Kemirtlek, Nizamettin, Sakar, Cihad, Erdem, Deniz, Ceylan, Gülay Güleç, Turan, Işıl Özkoçak, Kazancıoğlu, Sümeyye, Bodur, Hürrem
Publicado 2021