Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Seha Saygili"'
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:
Kubra Yilmaz, Seha Saygili, Nur Canpolat, Ozlem Akgun-Dogan, Zeynep Nagehan Yuruk Yildirim, Rumeysa Yasemin Cicek-Oksuz, Huseyin Adil Oner, Bagdagul Aksu, Nazli Gulsum Akyel, Ozge Oguzhan-Hamis, Hasan Dursun, Sevgi Yavuz, Neslihan Cicek, Nurver Akinci, Esra Karabag Yilmaz, Ayse Agbas, Ahmet Nevzat Nayir, Dildar Konukoglu, Sebuh Kurugoglu, Lale Sever, Salim Caliskan
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionIn the pediatric context, most children with autosomal dominant polycystic kidney disease (ADPKD) maintain a normal glomerular filtration rate (GFR) despite underlying structural kidney damage, highlighting the critical need for early int
Externí odkaz:
https://doaj.org/article/8abcc0af6a03406cad97d638a3faf51a
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:
Kaya Saribeyoglu, Erman Aytac, Salih Pekmezci, Seha Saygili, Hafize Uzun, Gulsen Ozbay, Seval Aydin, Hakki Oktay Seymen
Publikováno v:
Asian Journal of Surgery, Vol 34, Iss 4, Pp 153-157 (2011)
Background/Objective: Clinoptilolite is a natural zeolite crystal. Cytoprotective effects of clinoptilolite have been reported. However, so far there are no data about the effects of clinoptilolite treatment on oxidative stress after partial hepatect
Externí odkaz:
https://doaj.org/article/7a1df46615674e20b3e997023ac3261b
Autor:
Seval Aydin, Erman Aytac, Hafize Uzun, Tuncay Altug, Banu Mansur, Seha Saygili, Nur Buyukpinarbasili, Muzaffer Sariyar
Publikováno v:
Asian Journal of Surgery, Vol 33, Iss 4, Pp 173-180 (2010)
Obstructive jaundice develops after occlusion of the common bile duct. Direct hyperbilirubinaemia, which occurs secondary to the condition, causes various life-threatening pathologies. Cytoprotective effects of Ganoderma lucidum (GL) have previously
Externí odkaz:
https://doaj.org/article/e348eeb67c41408490a406353cba45e2
Autor:
Seha, Saygili, Mehmet, Kocaaga, Gamze, Kaya, Mine, Sukur, Firdevs, Bas, Sukran, Poyrazoglu, Ruveyde, Bundak, Feyza, Darendeliler
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:69-80
Reports on the association between growth hormone therapy and cardiovascular risk factors in children are limited. This study aimed to evaluate carotid intima-media thickness (cIMT) in children treated with recombinant human growth hormone (rhGH) and
Autor:
Ozge Hurdogan, Fatmanur Karakus, Ahmet Burak Dirim, Bagdagul Aksu, Seha Saygili, Aydin Turkmen, Alev Yilmaz, Nur Canpolat, Seyhun Solakoglu, Isin Kilicaslan, Yasemin Ozluk
Publikováno v:
Applied Immunohistochemistry & Molecular Morphology. 31:224-231
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:
Matko Marlais, Tanja Wlodkowski, Nikoleta Printza, Dorothea Kronsteiner, Regina Krisam, Lukas Sauer, Marina Aksenova, Isa Ashoor, Atif Awan, Justine Bacchetta, Ramnath Balasubramanian, Biswanath Basu, Zivile Bekassy, Olivia Boyer, Eugene Yu-hin Chan, Dagmar Csaicsich, Stéphane Decramer, Eiske Dorresteijn, Magdalena Drozynska-Duklas, Loai Akram Eid, Laura Espinosa, Verónica Ferraris, Hana Flögelová, Jessica Forero-Delgadillo, Alessandra Gianviti, Valentina Gracchi, Mercedes López González, Matthias Hansen, Motoshi Hattori, Xu Hong, Nakysa Hooman, Dmytro Ivanov, Hee Gyung Kang, Vasiliki Karava, Ina Kazyra, Adrian Lungu, Stephen Marks, Andrew Maxted, Anna Moczulska, Rebekka Müller, Tatiana Nastausheva, Mattia Parolin, Carmine Pecoraro, Iliana Principi, Cheryl Sanchez-Kazi, Seha Saygili, Raphael Schild, Mohan Shenoy, Rajiv Sinha, Ana Paula Spizzirri, Maria Stack, Maria Szczepanska, Alexey Tsygin, Julia Tzeng, Vaidotas Urbonas, Carlos Zapata, Jakub Zieg, Franz Schaefer, Marina Vivarelli, Kjell Tullus
Publikováno v:
American Journal of Kidney Diseases, 81(1), 119-122. W B SAUNDERS CO-ELSEVIER INC
American Journal of Kidney Diseases, 81(1), 119-122. W.B. Saunders
American Journal of Kidney Diseases, 81(1), 119-122. W.B. Saunders
Autor:
Tugba Tastemel Ozturk, Nur Canpolat, Seha Saygili, Umut Selda Bayrakci, Oguz Soylemezoglu, Fatih Ozaltin, Rezan Topaloglu
Recently, recessive mutations in SGPL1 (sphingosine-1-phosphate lyase), which encodes the final enzyme of sphingolipid metabolism, have been reported to cause steroid-resistant nephrotic syndrome, adrenal insufficiency, and many other organ/system in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d47884959f152f22cba784d882f9a7e6
https://avesis.gazi.edu.tr/publication/details/0a36e17f-779a-4136-952b-1f372521288c/oai
https://avesis.gazi.edu.tr/publication/details/0a36e17f-779a-4136-952b-1f372521288c/oai