Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fatih Özaltın"'
Autor:
Rezan Topaloglu, Ayşe Gültekingil Keser, Bora Gülhan, Fatih Ozaltin, Hülya Demir, Türkmen Çiftci, Numan Demir, Çağrı Mesut Temucin, Aysel Yuce, Okhan Akhan
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background Cystinosis is a multisystemic disease resulting from cystine accumulation primarily in kidney and many other tissues. We intended to study the evolution of less commonly seen extrarenal complications of cystinosis in a group of pa
Externí odkaz:
https://doaj.org/article/892e8d37c2be497ea606f2735e785b1c
Autor:
Rezan Topaloglu, Ayşe Gültekingil, Bora Gülhan, Fatih Ozaltin, Hülya Demir, Türkmen Çiftci, Numan Demir, Çağrı Mesut Temucin, Aysel Yuce, Okhan Akhan
Publikováno v:
BMC Gastroenterology, Vol 22, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/4304b247cf21457ea431bd27c1b32ef4
Autor:
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, Olivier Gribouval, Szymon Ziętkiewicz, Jameela A Kari, Mohamed A Shalaby, Fatih Ozaltin, Jiri Dusek, Anette Melk, Aysun K Bayazit, Laura Massella, Lidia Hyla-Klekot, Sandra Habbig, Astrid Godron, Maria Szczepańska, Beata Bieniaś, Dorota Drożdż, Rasha Odeh, Wioletta Jarmużek, Katarzyna Zachwieja, Agnes Trautmann, Corinne Antignac, Franz Schaefer, PodoNet Consortium
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0180926 (2017)
Schimke immuno-osseous dysplasia (SIOD) is a rare multisystem disorder with early mortality and steroid-resistant nephrotic syndrome (SRNS) progressing to end-stage kidney disease. We hypothesized that next-generation gene panel sequencing may unsurf
Externí odkaz:
https://doaj.org/article/ea42cc11ba6a483999137f6d15f84b6c
Autor:
Eda Didem Kurt-Şükür, Bora Gülhan, Gülşah Özdemir, Tuğba Taştemel Öztürk, Demet Baltu, Fatih Özaltın, Ali Düzova, Rezan Topaloğlu
Publikováno v:
Turkish Journal of Nephrology, Vol 32, Iss 4, Pp 353-360 (2023)
Externí odkaz:
https://doaj.org/article/e9e472e54ae1402d8977ce57543577ac
Autor:
Evra, Çelikkaya, Tülin, Güngör, Deniz, Karakaya, Evrim, Kargın Çakıcı, Fatma, Yazılıtaş, Fatih, Özaltın, Mehmet, Bülbül
Publikováno v:
Experimental and Clinical Transplantation. 20:45-48
Membranoproliferative glomerulonephritis and renal microangiopathies may manifest similar clinical presentations and histology. Many genetic mutations that cause these diseases have been reported. Studies on mutations in the gene encoding diacylglyce
Autor:
Gözdem Kaykı, Diclehan Orhan, Bora Gülhan, Rezan Topaloğlu, Zuhal Akçören, Ali Düzova, Fatih Özaltın, Seza Özen, Yelda Bilginer, Şafak Güçer
Publikováno v:
The Turkish journal of pediatrics. 64(1)
Crescentic glomerulonephritis (CGN) is a rapidly progressive and rare cause of glomerulonephritis in childhood. The aim of this study is to evaluate demographic data of children with crescentic glomerulonephritis, to classify the etiologies and to in
Autor:
Bora, Gülhan, Fatih, Özaltın
Publikováno v:
Turkish archives of pediatrics. 56(5)
Hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy (TMA), mainly affecting the kidney. The disease is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. It is one of the most common causes of a
Autor:
Sare Gülfem Özlü, Bora Gülhan, Özlem Aydoğ, Emine Atayar, Ali Delibaş, Gönül Parmaksız, Elif Bahat Özdoğan, Elif Çomak, Mehmet Taşdemir, Banu Acar, Zeynep Birsin Özçakar, Rezan Topaloğlu, Oğuz Söylemezoğlu, Fatih Özaltın
Publikováno v:
Turkish Journal of Pediatrics
Background: atypical hemolytic uremic syndrome (aHUS) occurs due to defective regulation of the alternative complement pathway (ACP) on vascular endothelial cells. Plasma based therapy (PT) was the mainstay of the treatment for aHUS for many years un
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Autor:
Emirhan Nemutlu, Fatih Ozaltin, Samiye Yabanoglu-Ciftci, Bora Gulhan, Cemil Can Eylem, İpek Baysal, Elif Damla Gök-Topak, Kezban Ulubayram, Osman Ugur Sezerman, Gulberk Ucar, Sedef Kır, Rezan Topaloglu
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2603 (2023)
Cystinosis is a rare, devastating hereditary disease secondary to recessive CTNS gene mutations. The most commonly used diagnostic method is confirmation of an elevated leukocyte cystine level; however, this method is expensive and difficult to perfo
Externí odkaz:
https://doaj.org/article/e37bd383588b4a949b8510db4a1252d3