Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Fatih Özaltın"'
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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Kurt-Şükür, Eda Didem1, Gülhan, Bora1, Özdemir, Gülşah1, Öztürk, Tuğba Taştemel1, Baltu, Demet1, Özaltın, Fatih1, Düzova, Ali1, Topaloğlu, Rezan1 rezantopaloglu@hacettepe.edu.tr
Publikováno v:
Turkish Journal of Nephrology. Oct2023, Vol. 32 Issue 4, p353-360. 8p.
Publikováno v:
Pediatric Nephrology. 2023 Suppl2, Vol. 38, p43-257. 215p. 10 Color Photographs, 2 Black and White Photographs, 15 Diagrams, 47 Charts, 56 Graphs.
Autor:
Improda, Nicola1,2 nicolaimproda@gmail.com, Rosanio, Francesco1, De Martino, Lucia3, Picariello, Stefania3, Mozzillo, Enza1, Franzese, Adriana1, Quaglietta, Lucia3
Publikováno v:
Turkish Archives of Pediatrics. Jan2023, Vol. 58 Issue 1, p115-118. 4p.
Publikováno v:
Pediatric Nephrology. Oct2021, Vol. 36 Issue 10, p3285-3491. 207p. 1 Color Photograph, 14 Charts, 8 Graphs.