Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Orhan Görukmez"'
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 11, Iss 2, Pp 133-136 (2024)
In some cases, making of physical abuse diagnosis can be difficult if the findings were derived from an unusual disease or an unexpected finding of a common disease. A female infant was admitted to emergency department of our hospital, who was suffer
Externí odkaz:
https://doaj.org/article/f5415a8843c44f4984decb6d2c990fd0
Autor:
Orhan Gorukmez, Ozlem Gorukmez, Ali Topak, Meral Seferoglu, Ali O Sivaci, Asuman Ali, Nermin Tepe, Sibel C Kabay, Ozlem Taskapilioglu
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 4, Pp 484-490 (2023)
Background: Cerebral autosomal dominant arteriopathy with subcortical infarctions and leukoencephalopathy (CADASIL) is the most common hereditary form of cerebral small vessel disease. It is clinically, radiologically, and genetically heterogeneous a
Externí odkaz:
https://doaj.org/article/6029d47c199540d0940b793ba7a031e5
Autor:
Nafiye Emel Çakar, Orhan Görükmez
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 3, Pp 372-378 (2021)
Objective: 3-Hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency is a rare metabolic disease of valine metabolism. Only 22 cases of HIBCH deficiency have been reported in the literature. Our algorithm could help in the diagnosis of this disease. Metho
Externí odkaz:
https://doaj.org/article/74db4053e6fb4c2795db2a21837fc712
Autor:
Veysel GOK, Firdevs AYDIN, Alper OZCAN, Ebru YILMAZ, Ekrem UNAL, Musa KARAKUKCU, Türkan PATIROGLU, Mehmet Akif OZDEMIR, Filiz KARAMAN, Orhan GORUKMEZ, Ozlem GORUKMEZ, Atil BISGIN
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S65- (2021)
Objective: The programmed cell death 1 (PD-1) receptor is an immune checkpoint receptor expressed by activated T cells. PD-1 inhibits the immune system by binding to its ligands expressed on tumor cells. Nivolumab and pembrolizumab are some of the mo
Externí odkaz:
https://doaj.org/article/8fc9fac9b6054cc2b9b1c3e60f6e9bd4
Autor:
Mustafa Ferhat Öksuz, Mutlu Karkucak, Orhan Görukmez, Gökhan Ocakoğlu, Abdulmecit Yıldız, Mehmet Ture, Tahsin Yakut, Kamil Dilek
Publikováno v:
Revista Brasileira de Reumatologia, Vol 57, Iss 6, Pp 501-506
Abstract Aim: Various mutations have been identified in the Mediterranean fever (MEFV) gene which is reported to be responsible from Familial Mediterranean fever (FMF). In our study, we aimed to determine the frequency of the MEFV mutations in our re
Externí odkaz:
https://doaj.org/article/e9df650824be4705a663d07ac8d72b56
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 59, Iss 5, Pp 706-710 (2020)
Objective: Intrahepatic cholestasis of pregnancy (ICP) is a liver disorder of pregnancy characterized by pruritus, elevated liver enzymes and fasting serum bile acids. Genetic predisposition has been suggested to play a role in its etiology and mutat
Externí odkaz:
https://doaj.org/article/184f5564257c4bc5ae45d9df005dca55
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 3, Pp 401-403 (2020)
Externí odkaz:
https://doaj.org/article/7e02545ed5d04a93984a9abdc8768b3c