Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ali Düzova"'
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:
Rezan Topaloğlu, Bora Gülhan, Kübra Çelegen, Mihriban İnözü, Mutlu Hayran, Ali Düzova, Fatih Ozaltin
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Since the early 2000s rituximab (RTX) has been thought of as an alternative treatment for steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS).Objective: This study aimed to determine the effects of
Externí odkaz:
https://doaj.org/article/ba2bafb54d29480da67579f47dfe1fb4
Autor:
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
Publikováno v:
Pediatric Nephrology.
Autor:
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
Publikováno v:
Pediatric Nephrology.
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:
Anar Gurbanov, Bora Gülhan, Barış Kuşkonmaz, Fatma Visal Okur, Fatih Ozaltin, Ali Düzova, Duygu Uçkan Çetinkaya, Rezan Topaloglu
Publikováno v:
Pediatric nephrology (Berlin, Germany).
This study aimed to determine incidence of kidney complications in pediatric allogeneic hematopoietic stem cell transplantation (HSCT) patients.Pediatric allogeneic HSCT patients were included. Post-transplantation urinary system complications were c
Publikováno v:
The Turkish Journal of Pediatrics. 65:1
Autor:
Bagdagul Aksu, Alberto Caldas Afonso, Ipek Akil, Harika Alpay, Bahriye Atmis, Ozlem Aydog, Sevcan Bakkaloglu, Aysun Karabay Bayazıt, Meral Torun Bayram, Ilmay Bilge, Ipek Kaplan Bulut, Ayse Pinar Goksu Cetinkaya, Elif Comak, Belde Kasap Demir, Nida Dincel, Osman Donmez, Mehmet Akif Durmus, Hasan Dursun, Ruhan Dusunsel, Ali Duzova, Pelin Ertan, Asuman Gedikbasi, Nilufer Goknar, Sercin Guven, Duygu Hacihamdioglu, Augustina Jankauskiene, Mukaddes Kalyoncu, Salih Kavukcu, Bahriye Uzun Kenan, Nuran Kucuk, Bahar Kural, Mieczysław Litwin, Giovanni Montini, William Morello, Lukasz Obrycki, Beyhan Omer, Ebru Misirli Ozdemir, Nese Ozkayin, Dusan Paripovic, Cemile Pehlivanoglu, Seha Saygili, Franz Schaefer, Susanne Schaefer, Ferah Sonmez, Yilmaz Tabel, Nesrin Tas, Mehmet Tasdemir, Ana Teixeira, Demet Tekcan, Rezan Topaloglu, Sebahat Tulpar, Ozde Nisa Turkkan, Berfin Uysal, Metin Uysalol, Renata Vitkevic, Sevgi Yavuz, Sibel Yel, Tarik Yildirim, Zeynep Yuruk Yildirim, Nurdan Yildiz, Selcuk Yuksel, Eray Yurtseven, Alev Yilmaz
Publikováno v:
Frontiers in Urology, Vol 3 (2024)
BackgroundCongenital anomalies of the kidney and urinary tract (CAKUT) are defined as structural malformations of the kidney and/or urinary tract. Heat shock proteins (HSPs) are expressed in the kidney in response to cellular changes, such as thermal
Externí odkaz:
https://doaj.org/article/a80c88e2313546b599114335aabc3870
Autor:
Lale Guliyeva, Yılmaz Tabel, Ali Düzova, Nusret Akpolat, Seza Özen, Rezan Topaloğlu, Betül Sözeri
Publikováno v:
Pediatric Nephrology. 35:619-620
Autor:
Rosalie Sterenborg, Irena Jankowska, Malgorzata Stanczyk, Anna Niemirska, Max Christoph Liebau, ALI DÜZOVA, Dorota Wicher, Bjoern Buchholz, Rukshana Shroff, Patryk Lipinski, Marcin Tkaczyk, ASLIHAN KARA, Salih Kavukcu, Jolanta Antoniewicz, Przemyslaw Sikora, Dušan Paripović, Mieczyslaw Litwin, SELCUK YUKSEL, Nur Canpolat, İbrahim Gökce, Miguel Garcia Gonzalez, Larisa Prikhodina, Maria Szczepanska, Karolis Azukaitis, Ann Raes, Djalila Mekahli, Svetlana Papizh, Julia Hoefele, Kevin Kunzmann, Hulya Nalcacioglu, Katarzyna Taranta-Janusz, Salim Çalışkan, Alberto Caldas Afonso
Publikováno v:
Europe PubMed Central
Frontiers in Pediatrics
FRONTIERS IN PEDIATRICS
Frontiers in Pediatrics
FRONTIERS IN PEDIATRICS
Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phenotype often presenting prenatally or in early childhood. With its obligate renal and hepatic involvement, ARPKD is one of the most important indicatio