Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Onur Cura D."'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 18, Iss 1, Pp 65-70 (2015)
The CHARGE (coloboma, heart defects, atresia, retardation, genital, ear) syndrome is a genetic disease characterized by ocular coloboma, choanal atresia or stenosis and semicircular canal abnormalities. Most of the patients clinically diagnosed with
Externí odkaz:
https://doaj.org/article/3ed29d0d886f4af289e3d101863573e1
Autor:
Onur Cura D; Faculty of Medicine, Department of Medical Genetics, Dokuz Eylul University, Izmir, Turkey., Yildiz S; Faculty of Medicine, Department of Nephrology, Dokuz Eylul University, Izmir, Turkey., Ataman E; Faculty of Medicine, Department of Medical Genetics, Dokuz Eylul University, Izmir, Turkey., Ersan S; Department of Nephrology, Tepecik Education and Research Hospital, University of Health Sciences, İzmir, Turkey., Tanrisev M; Department of Nephrology, Tepecik Education and Research Hospital, University of Health Sciences, İzmir, Turkey., Ulgenalp A; Faculty of Medicine, Department of Medical Genetics, Dokuz Eylul University, Izmir, Turkey., Camsari T; Faculty of Medicine, Department of Nephrology, Dokuz Eylul University, Izmir, Turkey., Ercal D; Faculty of Medicine, Department of Pediatric Genetics, Dokuz Eylul University, Izmir, Turkey.
Publikováno v:
Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy [Ther Apher Dial] 2021 Feb; Vol. 25 (1), pp. 97-102. Date of Electronic Publication: 2020 Jun 01.
Autor:
Onur Cura D; Department of Molecular Medicine, Institute of Health Sciences, Dokuz Eylul University, 35330 Izmir, Turkey. duyguonur_05@hotmail.com.
Publikováno v:
International journal of molecular sciences [Int J Mol Sci] 2019 Oct 01; Vol. 20 (19). Date of Electronic Publication: 2019 Oct 01.
Publikováno v:
Cytogenetic and genome research [Cytogenet Genome Res] 2019; Vol. 158 (2), pp. 83-87. Date of Electronic Publication: 2019 Jun 14.
Autor:
Onur Cura D; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey. Electronic address: duyguonur_05@hotmail.com., Iscan B; Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey., Gursoy S; Division of Pediatric Genetic Disorders, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey., Guleryuz H; Division of Pediatric Radiology, Department of Radiology, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey., Cankaya T; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey., Ozturk T; Division of Pediatric Radiology, Department of Radiology, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey., Giray Bozkaya O; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey; Division of Pediatric Genetic Disorders, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Publikováno v:
Pediatrics and neonatology [Pediatr Neonatol] 2017 Oct; Vol. 58 (5), pp. 455-457. Date of Electronic Publication: 2016 Nov 28.
Autor:
Çankaya, Tufan1, Cura, Duygu Onur2 duyguonur_05@hotmail.com, Özkalaycı, Hande1, Ülgenalp, Ayfer2
Publikováno v:
Erciyes Medical Journal / Erciyes Tip Dergisi. 2021, Vol. 43 Issue 2, p166-169. 4p.
Publikováno v:
Duzce Medical Journal. 2020, Vol. 22 Issue 3, p226-229. 4p.
Autor:
Bora, Feyza, Aslan, Bengisu, Sarı, Funda, Yılmaz, Fatih, Ersoy, Fettah Fevzi, Köksoy, Sadi, Özdem, Sebahat, Küçükçetin, İkbal Özen, Sipahioğlu, Murat, Karakaya, İbrahim, Koç, Yener, Ulu, Memnune Sena
Publikováno v:
Therapeutic Apheresis & Dialysis; Apr2023, Vol. 27 Issue 2, p353-360, 8p
Publikováno v:
Clinical Endocrinology; Jul2022, Vol. 97 Issue 1, p3-12, 10p
Autor:
Peining Li, Thomas Liehr
This book presents chromosome-wise clinical cases following an evidence-based protocol, in addition to providing the scientific background on the mechanisms of human ring chromosome (RC) formation. Presence of RCs in a genome can lead to several rare
