Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Demet, Teker Düztaş"'
Autor:
Ödül Eğribaş Gürkan, Hakan Öztürk, Cem Kaya, Neslihan Gürcan Kaya, Neslihan Ekşi Bozbulut, Ayşe Can, Kamercan Ceylan, Aysel Ünlüsoy Aksu, Demet Teker Düztaş, Sinan Sarı, Buket Dalgıç, Alparslan Kapısız, Demet Coşkun, Gökcen emmez, Gözde İnan, İsmail Akdulum, Hasan Kutlu Pampal, Nuray Camgoz Eryılmaz, Selin Erel, Volkan Şıvgın, Ercan Yıldırım, Okan Ermiş, İrfan Güngör, Gülay Kip, Nurdan Bedirli, Berrin Işık, İbrahim Onur Özen, Yusuf Hakan Çavuşoğlu, Ramazan Karabulut, Zafer Türkyılmaz, Kaan Sönmez
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 35, Iss 3, Pp 255-261 (2024)
Background/Aims: Gastric outlet obstruction (GOO) is a rare condition in childhood, with the exception of infantile hypertrophic pyloric stenosis (IHPS). However, no classification exists from a pediatric gastroenterologist’s perspective. Materi
Externí odkaz:
https://doaj.org/article/5449add8de5843c5bc86c94133a0f4af
Autor:
Demet, Teker Düztaş, Sinan, Sarı, Ödül, Eğritaş Gürkan, Gülsüm, Kayhan, Aydın, Dalgıç, Buket, Dalgıç
Publikováno v:
Experimental and Clinical Transplantation. 20:115-117
Ciliopathies are a heterogeneous group of diseases that are observed after deterioration of the ciliary structures on the cell surface that facilitate communication with the environment. Both liver and kidney involvement are frequently observed in th
Autor:
Demet Teker Düztaş, Sinan Sari, Ödül Eğritaş Gürkan, Mustafa Hakan Sözen, Buket Dalgiç, Aydın Dalgiç
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 20(Suppl 3)
Progressive familial intrahepatic cholestasis is a heterogeneous group of autosomal recessive disorders, and liver transplant is the only curative treatment. A biliary diversion operation for disruption of enterohepatic circulation in patients with p