Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Z. Birsin Özçakar"'
Autor:
Dilşah Önerli Salman, Zeynep Şıklar, Eda Nisa Çullas İlarslan, Z. Birsin Özçakar, Pınar Kocaay, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 46-54 (2019)
Objective:There is a growing interest in the relationship between obesity and renal damage. The effect of obesity on renal function in children and adolescents has not been adequately investigated. In addition, there is no complete consensus on the r
Externí odkaz:
https://doaj.org/article/a9063650493a465d8ddf753caf3ac025
Autor:
Eda Nisa Çullas İlarslan, Z. Birsin Özçakar, Pınar Kocaay, Dilsah Onerli Salman, Zeynep Şıklar, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 46-54 (2019)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Objective: There is a growing interest in the relationship between obesity and renal damage. The effect of obesity on renal function in children and adolescents has not been adequately investigated. In addition, there is no complete consensus on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e2152b980b7e28afd3fe70b4d97ac5
https://doi.org/10.4274/jcrpe.galenos.2018.2018.0046
https://doi.org/10.4274/jcrpe.galenos.2018.2018.0046
Autor:
Rezan Topaloglu, Mutlu Hayran, Emine Atayar, Oguz Soylemezoglu, Selçuk Yüksel, Mihriban İnözü, Bora Gülhan, Esra Baskin, Ozum Tutal, Fatih Ozaltin, Seha Saygili, Z. Birsin Özçakar, Ali Duzova
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Cystic kidney diseases are a heterogeneous group of chronic renal disease. Autosomal recessive polycystic kidney disease (ARPKD) is generally diagnosed in utero or at birth due to mutations in PKHD1 gene. Autosomal dominant polycy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::873a444d99990fa9f23ac88dfce58691
https://doi.org/10.1093/ndt/gfab081.008
https://doi.org/10.1093/ndt/gfab081.008
Autor:
Alper Soylu, Mutlu Hayran, Harika Alpay, Emine Atayar, Bora Gülhan, Oguz Soylemezoglu, Cengiz Candan, Fehime Kara Eroglu, Ayşe Ağbaş, Rezan Topaloglu, Nur Canpolat, Belde Kasap Demir, Z. Birsin Özçakar, Fatih Ozaltin, Selçuk Yüksel, Gulsah Ozdemir, Ali Duzova
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Alport syndrome (AS) is an inherited glomerular basement membrane disease caused by mutations in COL4A3, COL4A4 or COL4A5 genes. Recently, it has been reported that focal segmental glomerulosclerosis (FSGS) can be seen in AS and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9e041acdc839232163a02c33550bb4a
https://doi.org/10.1093/ndt/gfaa142.p0063
https://doi.org/10.1093/ndt/gfaa142.p0063
Autor:
Rezan Topaloglu, Z. Birsin Özçakar, Fatih Ozaltin, Fehime Kara Eroglu, Ali Duzova, Safak Gucer, Fatma Tuba Eminoğlu, Diclehan Orhan, Nazli Gonc, Rahsan Gocmen, Ayfer Alikasifoglu, Dilek Yalnizoglu, Hulya Nalcacioglu
Publikováno v:
Pediatric Neurology. 88:71-74
Ozcakar, Zeynep/0000-0002-6376-9189; DUZOVA, ALI/0000-0002-4365-2995; Gocmen, Rahsan/0000-0002-0223-9336 WOS: 000455971500011 PubMed: 30337132 BACKGROUND: COQ2 mutations cause a rare infantile multisystemic disease with heterogeneous clinical feature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7608d9c486249f8b7e0e04925298b7b
https://doi.org/10.1016/j.pediatrneurol.2018.07.008
https://doi.org/10.1016/j.pediatrneurol.2018.07.008
Autor:
Z. Birsin Özçakar, Semanur Özdel, Elif Çelikel, Nilgün Çakar, Seda Sahin, Fatma Aydın, Fatoş Yalçınkaya
Publikováno v:
Modern Rheumatology. 29:647-650
Objectives: Familial Mediterranean fever (FMF) is an autosomal recessive disease characterised by recurrent, self-limited attacks of fever with serositis. Recently, it was shown that FMF patients with early disease onset have more severe disease. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc0cfd0dfa224701d290608da69ae952
https://doi.org/10.1080/14397595.2018.1500874
https://doi.org/10.1080/14397595.2018.1500874
Autor:
Elif Çelikel, Atilla Halil Elhan, Z. Birsin Özçakar, Fatma Aydın, Nilgün Çakar, Semanur Özdel, Fatoş Yalçınkaya
Publikováno v:
Modern Rheumatology. 28:1016-1020
Familial Mediterranean fever (FMF) is characterized by recurrent, self-limited attacks of fever with serositis involving the peritoneum, pleura and joints. Fatigue is a common problem in many pediatric rheumatic diseases; however, has not been evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8d6401d4e82937f2cf5bdcc8d503bcf
https://doi.org/10.1080/14397595.2018.1427459
https://doi.org/10.1080/14397595.2018.1427459
Autor:
Songül Yılmaz, Nilgün Çakar, Banu Acar, Oguz Soylemezoglu, Bora Gülhan, Ayse Yurt, Elif Bahat, Z. Birsin Özçakar, Mustafa Koyun, Fatoş Yalçınkaya, Fatih Ozaltin, Emine Korkmaz
Publikováno v:
Nephron. 139:211-218
Agbas, Ayse/0000-0002-3658-8622; Ozcakar, Zeynep/0000-0002-6376-9189; Cakar, Nilgun/0000-0002-1853-0101 WOS: 000437355600002 PubMed: 29533929 Background: There are limited data on infants with atypical hemolytic uremic syndrome (aHUS). The aim of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a0e82ca77d185b68cc519cc938f6560
https://doi.org/10.1159/000487609
https://doi.org/10.1159/000487609
Autor:
Z. Birsin Özçakar, Fatoş Yalçınkaya
Publikováno v:
Pediatric nephrology (Berlin, Germany). 35(12)
Antenatal hydronephrosis (AHN) is the most frequently detected abnormality by prenatal ultrasonography. Differential diagnosis of AHN includes a wide variety of congenital abnormalities of the kidney and urinary tract ranging from mild abnormalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0830a0b7324647cd2b3c034097f27f8d
https://pubmed.ncbi.nlm.nih.gov/31811536
https://pubmed.ncbi.nlm.nih.gov/31811536
Autor:
Tülay Becerir, Havva Evrengül, Z. Birsin Özçakar, Fatih Ozaltin, Nagihan Yalçın, Emine Korkmaz, Selçuk Yüksel
Publikováno v:
Pediatric Drugs. 18:413-420
Introduction: Studies relating to first-line, early, and long-term eculizumab treatment and outcomes in children with atypical hemolytic uremic syndrome (aHUS) are scarce and unclear. The aim of this case-series study was to evaluate the outcomes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e130be89755aed383af967fe29fa045
https://doi.org/10.1007/s40272-016-0194-0
https://doi.org/10.1007/s40272-016-0194-0