Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Nurçin Saka"'
Autor:
Sukran Yildirim, Evrim Kiray Bas, Firdevs Bas, Tulay Guran, Feyza Darendeliler, Asuman Coban, Banu Kucukemre Aydin, Nurçin Saka
Publikováno v:
Journal of the Endocrine Society
Context: Limited data are available on the exact incidence of disorders of sex development (DSD) with genital ambiguity at birth. Objective: To determine frequency of ambiguous genitalia in newborns. Design: Prospective multicenter study. Setting: Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7708113fcafd76d3af79ddf83058b9be
https://doi.org/10.1210/js.2018-00408
https://doi.org/10.1210/js.2018-00408
Autor:
Rüveyde Bundak, Yasin Yilmaz, Bülent Erol, Melike Tuğrul, Aylin Yetim Şahin, Adem Ucar, Feyza Darendeliler, Kemal Nisli, Seher Yıldız, Ensar Yekeler, Banu Kucukemre Aydin, Nurçin Saka, Sukran Poyrazoglu, Firdevs Bas
Publikováno v:
Pediatric Cardiology. 39:786-793
Factors associated with aortic dilation and dissection in patients with Turner syndrome (TS) remain unclear. We assessed magnetic resonance imaging-based aortic diameters at nine predefined anatomic positions and examined associations of increased ao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88f2e5c5530d51c52f4a8901082c673d
https://doi.org/10.1007/s00246-018-1821-z
https://doi.org/10.1007/s00246-018-1821-z
Publikováno v:
Journal of Ege University School of Dentistry. 36:10-18
Turner’s syndrome (TS) is a sex chromosome disorder associated with a female phenotype. The loss of all or part of X chromosome that is affected the shape and the size of craniofacial structures in TS. Several studies have revealed concerning oral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73ff3b2a319ef42e24f72a7b5e3272f4
https://doi.org/10.5505/eudfd.2015.78941
https://doi.org/10.5505/eudfd.2015.78941
Autor:
Nurçin Saka, Oya Ercan, Nihal Memioglu, Tulay Guran, Belma Haliloglu, Pinar Isguven, Yasin Yilmaz, Filiz Tutunculer, Digdem Bezen, Filiz Mine Çizmecioğlu, Feyza Darendeliler, Banu Kucukemre Aydin, Firdevs Bas, Serap Turan, Sukran Poyrazoglu, Nurcan Cebeci, Rüveyde Bundak, Gül Yeşiltepe Mutlu, Abdullah Bereket, Şükrü Hatun
Study Objective To investigate the characteristics of children with ovarian cysts and evaluate treatment strategies. Design Retrospective study. Setting Eight pediatric endocrinology clinics, Turkey. Participants A total of 100 children and adolescen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21acacfad3afb87de0410073e6b6326
https://hdl.handle.net/20.500.12619/71408
https://hdl.handle.net/20.500.12619/71408
Autor:
Oğuz Bülent Erol, Ravza Yilmaz, Ayaz Aghayev, Sukran Poyrazoglu, Ensar Yekeler, Nurçin Saka, Dilek Sahin
Publikováno v:
Polish Journal of Radiology
Summary Background The aim of this study was to describe the gray-scale and color Doppler ultrasonography (US) and magnetic resonance (MR) imaging features of testicular adrenal rest tumors (TART) in patients with congenital adrenal hyperplasia. Mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad3e496758be2070dda80d7be278654a
https://ruj.uj.edu.pl/xmlui/handle/item/46080
https://ruj.uj.edu.pl/xmlui/handle/item/46080
Publikováno v:
SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital. :109-12
Evaluation of the neonates with anomalies of the external genitalia in our hospital Objective: To determine the prevalance of external genital abnormalities among neonates in our hospital. Material and Method: A total 3437 neonates delivered at Sisli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::844d1f2010a9fba68224bfc9268f0139
https://doi.org/10.5350/semb.20140130040119
https://doi.org/10.5350/semb.20140130040119
Autor:
Rüveyde Bundak, Hülya Günöz, Andrzej Furman, Firdevs Bas, Nurçin Saka, Feyza Darendeliler, Olcay Neyzi
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Standard deviation score or Z-score reference charts are used in some countries in preference to percentile charts and are considered as better tools in assessing children with measurements outside the accepted limits of normality. G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d6d901c3e08bde33a0a438d3a4d6c3
https://doi.org/10.4274/jcrpe.1260
https://doi.org/10.4274/jcrpe.1260
Autor:
Feyza Darendeliler, Nurçin Saka, Ahmet Uçar, Rüveyde Bundak, Firdevs Bas, Ceren Çetin, Sukran Poyrazoglu
Publikováno v:
Endocrine. 47:816-824
Children born large for gestational age (LGA) may be at risk for development of obesity and insulin resistance (IR). The reciprocal relationship of adipokines and proinflammatory cytokines is suggested to play a putative role in fine tuning of insuli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::438d04afcd62c23fdbb5f3a02e91a98f
https://doi.org/10.1007/s12020-014-0207-0
https://doi.org/10.1007/s12020-014-0207-0
Autor:
Rüveyde Bundak, Serdar Bozlak, Nurçin Saka, Nurdan Gul, İsmail Yildiz, Ahmet Uçar, Oğuz Bülent Erol, Ayse Kubat Uzum, Feyza Darendeliler, Sukran Poyrazoglu, Ensar Yekeler, Firdevs Bas
Publikováno v:
Clinical Endocrinology. 80:699-705
Precocious adrenarche (PA) refers to the clinical onset of excess androgen in girls before the age of 8. It is associated with an increased risk of functional ovarian hyperandrogenism after puberty. PA may be associated with polycystic ovary syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e29473c128b87a8c2bf062de61021c95
https://doi.org/10.1111/cen.12355
https://doi.org/10.1111/cen.12355
Autor:
Zeynep Tamay, Rüveyde Bundak, Ayşe Süleyman, Banu Küçükemre Aydın, Esen Özkaya, Feyza Darendeliler, Nermin Guler, Nurçin Saka, Gürkan Kılıç, Firdevs Baş
Publikováno v:
Pediatric Dermatology. 31:90-94
Netherton syndrome (NS) is a rare autosomal recessive disorder characterized by ichthyosiform scaling, hair abnormalities, and variable atopic features. Mutations in the serine protease inhibitor Kazal type 5 (SPINK5) gene leading to lymphoepithelial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b4532125aa36f32f4de1ec9da5c01b
https://doi.org/10.1111/pde.12220
https://doi.org/10.1111/pde.12220