Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cemile Pehlivanoğlu"'
Autor:
Bağdagül Aksu, Sevinç Emre, Alev Yılmaz, Zeynep Nagehan Yürük, Ümit Dilber Mutlu Demirel, Oğuz Bülent Erol, Cemile Pehlivanoğlu
Publikováno v:
Haseki Tıp Bülteni, Vol 57, Iss 2, Pp 122-128 (2019)
Aim:Nephrotic syndrome is a common type of kidney disease during childhood characterized by proteinuria, edema and hypoalbuminemia. Serum asymmetric dimethylarginine (ADMA) inhibits vascular nitric oxide production and may be an independent risk fact
Externí odkaz:
https://doaj.org/article/13c7c8e284004aac979055a26afaeacd
Autor:
Zeynep Yürük Yıldırım, Alev Yılmaz, Cemile Pehlivanoğlu, Asuman Gedikbaşı, Mehmet Yıldız, Ahmet Dirican, Rüveyde Bundak, Feyza Darendeliler, Sevinç Emre, Ahmet Nayır
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 157-163 (2019)
Objective:Histopathological changes in the kidney in type 1 diabetes mellitus (T1DM) begin before detection of microalbuminuria. Therefore, there is interest in finding a better biomarker for the early detection of diabetic kidney injury. The aim of
Externí odkaz:
https://doaj.org/article/d7efcdb1d32045419da069c13d00c435
Publikováno v:
Turkiye Klinikleri Journal of Case Reports. 30:55-58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07babcc3a5e7682eb468d4328f102a4f
https://doi.org/10.5336/caserep.2021-85827
https://doi.org/10.5336/caserep.2021-85827
Duplex Kidney Anomalies and Associated Pathologies in Children: A Single-Center Retrospective Review
Publikováno v:
Cureus. 14(6)
Duplex renal collecting systems are one of the most common congenital anomalies of the urinary tract. The exact prevalence of this anomaly is difficult to ascertain because most patients are asymptomatic, and the abnormality is frequently detected in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d0207c0ae1f46cfa6d7c3625f7f9934
https://pubmed.ncbi.nlm.nih.gov/35812643
https://pubmed.ncbi.nlm.nih.gov/35812643
Autor:
Serim Pul, İbrahim Gökçe, Ece Demirci Bodur, Serçin Güven, Neslihan Çiçek, Mehtap Sak, Özde Nisa Türkkan, Deniz Filinte, Cemile Pehlivanoğlu, Betül Sözeri, Harika Alpay
Publikováno v:
The Turkish Journal of Pediatrics. 65:330
Background. Antiphospholipid syndrome (APS), particularly the catastrophic antiphospholipid syndrome (CAPS), is one of the rare causes of thrombotic microangiopathy (TMA). CAPS is the most severe form of APS, especially when accompanied by complement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bdac6080a74e6cbb63b4b4d17e77e04
https://doi.org/10.24953/turkjped.2022.288
https://doi.org/10.24953/turkjped.2022.288
Publikováno v:
Pediatric Urology Case Reports.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe04a2cb74780862bd8372b1428742a1
https://doi.org/10.14534/j-pucr.2021267550
https://doi.org/10.14534/j-pucr.2021267550
Autor:
Cemile Pehlivanoğlu, Zeynep Yürük Yıldırım, Alev Yılmaz, Asuman Gedikbaşı, Nurinisa Karagöz, Nurver Akıncı, Aysel Kıyak, Gül Özçelik, Yasemin Özlük, Işın Kılıçaslan, Ayşe Özağarı, Bağdagül Yavaş Aksu, Sevinç Emre
Publikováno v:
Volume: 84, Issue: 4 568-573
Journal of Istanbul Faculty of Medicine
Journal of Istanbul Faculty of Medicine
Objective: The evidences from experimental and epidemiological studies suggests that elevated serum homocysteine levels may lead to renal injury and may be a significant risk factor for the development of chronic kidney disease. The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de55006e52b4395b2660c15fe45a1087
https://dergipark.org.tr/tr/pub/iuitfd/issue/64658/847530
https://dergipark.org.tr/tr/pub/iuitfd/issue/64658/847530
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