Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tuba Nur Tahtakesen Güçer"'
Autor:
Esra Arslantaş, Ali Ayçiçek, Sibel Akpınar Tekgündüz, Duygu Özkorucu Yıldırgan, Ayşe Özkan Karagenç, Tuba Nur Tahtakesen Güçer, Ayşe Gonca Kaçar, Cengiz Bayram, Nihal Özdemir
Publikováno v:
Turkish Archives of Pediatrics, Vol 59, Iss 2, Pp 193-199 (2024)
Objective: To investigate the effect of switching from deferasirox dispersible tablet (DT) to deferasirox film-coated tablet (FCT) on serum ferritin (SF) levels in transfusion-dependent patients. Materials and Methods: Patients who received regula
Externí odkaz:
https://doaj.org/article/5415c1b9a6b34f4a9c3a8f9b9e5cc3bf
Autor:
Ali Er, Arda Kayhan, Tevfik Guzelbey, Demet Deniz Doğancı, Ezgi Kartal, Zafer Salcioglu, Tuba Nur Tahtakesen Güçer, Nail Uzunlulu
Publikováno v:
İstanbul Kanuni Sultan Süleyman Tıp Dergisi. 13:74-79
Autor:
Ferhan Akici, Zafer Salcioglu, Ezgi Paslı Uysalol, Gül Nihal Özdemir, Cengiz Bayram, Elif Böncüoğlu, Gönül Aydoğan, Işık Odaman Al, Tuba Nur Tahtakesen Güçer, Gizem Ersoy, Müge Gökçe, Ali Aycicek
Publikováno v:
İstanbul Kanuni Sultan Süleyman Tıp Dergisi. 13:92-97
Autor:
Fahri Şahin, Ekrem Unal, Birol Baytan, Fatma Burcu Belen, Ferda Ozkinay, Yeşim Oymak, Vildan Çulha, Gülen Tüysüz, Adalet Meral Güneş, Kaan Kavakli, Bilçağ Akgün, Melike Sezgin Evim, Namik Ozbek, Alphan Kupesiz, Tahir Atik, Esra Isik, Hüseyin Onay, Moharram Shamsali, Can Balkan, Ebru Yılmaz Keskin, Zafer Salcioglu, Canan Albayrak, Tuba Nur Tahtakesen Güçer
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey,
Autor:
Gizem Ersoy, Nihal Özdemir, Salim Keskin, Cengiz Bayram, Ferhan Akici, Zafer Salcioglu, Gonul Aydogan, Ezgi Paslı Uysalol, Tuba Nur Tahtakesen Güçer
Publikováno v:
Journal of pediatric hematology/oncology. 41(4)
Most common causes of microcytic anemia in children are iron deficiency anemia (IDA) and thalassemia. Differentiation of these and detection of coexistence is essential for genetic counseling and to set a treatment plan. Aim is to characterize the fr
Autor:
Zafer Salcioglu, Gül Nihal Özdemir, Cengiz Bayram, Gonul Aydogan, Tugberk Akca, Tuba Nur Tahtakesen Güçer
Publikováno v:
Blood. 132:5887-5887
Aim: The aim of the study is to evaluate the efficacy, complications and long term results of splenectomy in children with hematologic diseases. Patients and Methods: This study includes retrospective analysis of the medical records of 158 children b