Zobrazeno 1 - 10
of 174
pro vyhledávání: '"Rezan, Topaloglu"'
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
Diversity of kidney care referral pathways in national child health systems of 48 European countries
Autor:
Velibor Tasic, Vidar O. Edvardsson, Evgenia Preka, Larisa Prikhodina, Constantinos J. Stefanidis, Rezan Topaloglu, Diamant Shtiza, Ashot Sarkissian, Thomas Mueller-Sacherer, Rena Fataliyeva, Ina Kazyra, Elena Levtchenko, Danka Pokrajac, Dimitar Roussinov, Danko Milošević, Avraam Elia, Tomas Seeman, Mia Faerch, Inga Vainumae, Janne Kataja, Michel Tsimaratos, Irakli Rtskhiladze, Peter F. Hoyer, George Reusz, Atif Awan, Danny Lotan, Licia Peruzzi, Nazim Nigmatullina, Nasira Beishebaeva, Edite Jeruma, Augustina Jankauskiene, Olivier Niel, Valerie Said-Conti, Angela Ciuntu, Snežana Pavićević, Michiel Oosterveld, Anna Bjerre, Marcin Tkaczyk, Ana Teixeira, Adrian C. Lungu, Alexey Tsygin, Vesna Stojanović, Ludmila Podracka, Tanja Kersnik Levart, Mar Espino-Hernández, Per Brandström, Giuseppina Sparta, Harika Alpay, Dmytro Ivanov, Jan Dudley, Komiljon Khamzaev, Dieter Haffner, Jochen Ehrich
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPrimary, secondary and tertiary healthcare services in Europe create complex networks covering pediatric subspecialties, sociology, economics and politics. Two surveys of the European Society for Paediatric Nephrology (ESPN) in 1998 and 201
Externí odkaz:
https://doaj.org/article/f14fb7b985dd4342a50d5e772886dda3
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
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:
Ezgi Ay, Emre Gurses, Filiz Aslan, Bora Gulhan, Asuman Alniacik, Ali Duzova, Munir Demir Bajin, Levent Sennaroglu, Gulsum Aydan Genc, Fatih Ozaltin, Rezan Topaloglu
Publikováno v:
Audiology and Neurotology. :1-10
Introduction: Distal renal tubular acidosis (dRTA) is a disease that may develop either primarily or secondarily, resulting from urinary acidification defects in distal tubules. Hearing loss may accompany primary forms of dRTA. This study aims to det
Autor:
Atif Awan, Michael Riordan, Ipek Kaplan Bulut, Sevgin Taner, Francesco Emma, Jakub Zieg, Olivia Boyer, Nakysa Hooman, Lars Pape, Robert Woroniecki, Timo Jahnukainen, Matthias Hansen, Sarah Wente-Schulz, Marina Aksenova, Cahyani Gita Ambarsari, Francesca Becherucci, Marc Fila, Telma Francisco, Ibrahim Gokce, Bora Gülhan, Mahmoud Kallash, Konstantinos Kamperis, Sherene Mason, Antonio Mastrangelo, Francesca Mencarelli, Bogna Niwinska-Faryna, Rina R Rus, Seha Saygili, Erkin Serdaroglu, Rezan Topaloglu, Enrico Vidal, Sibel Yel, Kathrin Buder, Elisabeth AM Cornelissen, Maria del Mar Espino Hernández, Markus Kemper, Julie Maquet, Fernando Santos, Ulrike Walden
Publikováno v:
BMJ Open, Vol 11, Iss 5 (2021)
Background Acute tubulointerstitial nephritis (TIN) is a significant cause of acute renal failure in paediatric and adult patients. There are no large paediatric series focusing on the aetiology, treatment and courses of acute TIN.Patients, design an
Externí odkaz:
https://doaj.org/article/cd48ca283f8a49d89cde2736d7e18d7c
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:
Ozum Tutal, Bora Gulhan, Emine Atayar, Selcuk Yuksel, Z. Birsin Ozcakar, Oguz Soylemezoglu, Seha Saygili, Salim Caliskan, Mihriban Inozu, Esra Baskin, Ali Duzova, Mutlu Hayran, Rezan Topaloglu, Fatih Ozaltin
Publikováno v:
Nephron. :1-14
Introduction: Autosomal recessive polycystic kidney disease (ARPKD) is associated with pathogenic variants in the PKHD1 gene. Autosomal dominant polycystic kidney disease (ADPKD) is mainly associated with pathogenic variants in PKD1 or PKD2. The pres
Autor:
Zsolt Bognar, Daniele De Luca, Magnus Domellöf, Adamos Hadjipanayis, Dieter Haffner, Mark Johnson, Sanja Kolacek, Berthold Koletzko, Miguel Saenz de Pipaon, Delane Shingadia, Pierre Tissieres, Luigi Titomanlio, Rezan Topaloglu, Johannes Trück
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Pediatric associations have been urged not to interact with and not to accept support from commercial providers of breast milk substitutes (BMSs), based on the assumption that such interaction would lead to diminished promotion and support of breastf
Externí odkaz:
https://doaj.org/article/aae537f3d5384e5aaeae1f710ec1ba72
Autor:
Katharina Hohenfellner, Ewa Elenberg, Gema Ariceta, Galina Nesterova, Neveen A. Soliman, Rezan Topaloglu
Publikováno v:
Cells, Vol 11, Iss 7, p 1109 (2022)
Newborn screening (NBS) programmes are considered to be one of the most successful secondary prevention measures in childhood to prevent or reduce morbidity and/or mortality via early disease identification and subsequent initiation of therapy. Howev
Externí odkaz:
https://doaj.org/article/5bf2274ef7f74bd9b5fdec43ba965123