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Serdar Ceylaner

Showing results (81-90 of 244) with videos related to

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Dermatologic Therapy|August 9, 2020
Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from TurkeyIşıl Göğem İmren, Efsun Tanacan, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|April 7, 2018
Beta-ketothiolase deficiency: An unusual cause of recurrent ketoacidosisGonca Kılıç-Yıldırım, Sultan Durmuş-Aydoğdu, Serdar Ceylaner, et al.
Brain & Development|December 24, 2014
Giant axonal disease: Report of eight casesFaruk Incecik, Ozlem M Herguner, Serdar Ceylaner, et al.
Clinics and Research in Hepatology and Gastroenterology|April 23, 2022
A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblingsKhaled Warasnhe, Figen Özçay, Halil İbrahim Aydin, et al.
The Journal of Obstetrics and Gynaecology Research|July 30, 2019
Analysis of TP53 gene in uterine myomas: No mutations but P72R polymorphism is associated with myoma developmentS Ozlem Altinkaya, Sumeyra N Avcioglu, Selda D Sezer, et al.
Anatolian Journal of Cardiology|December 20, 2017
A novel mutation in the desmoplakin gene in two female siblings with a rare form of dilated cardiomyopathy: Carvajal syndromeMehmet Gökhan Ramoğlu, Tayfun Uçar, Serdar Ceylaner, et al.
Archives of Gynecology and Obstetrics|April 5, 2007
Neu-Laxova syndrome, grossly appearing normal on 20 weeks ultrasonographic scan, that manifested late in pregnancy: a case reportSerkan Kahyaoglu, Inci Turgay, Ibrahim E Ertas, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 9, 2006
A case of fetal anticonvulsant syndrome with severe bilateral upper limb defectMelih Atahan Guven, Cem Batukan, Serdar Ceylaner, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Vici syndrome in siblings born to consanguineous parentsSener Tasdemir, Ibrahim Sahin, Atilla Cayır, et al.
Acta Neurologica Belgica|April 29, 2023
Could miglustat be a potential candidate in the treatment of action myoclonus renal failure syndrome?Seyda Erdoğan, Gül Yalçın Çakmaklı, Bülent Elibol, et al.
Pageof 25

Showing results (81-90 of 244) with videos related to

Sort By:
Pageof 25
Dermatologic Therapy|August 9, 2020
Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from TurkeyIşıl Göğem İmren, Efsun Tanacan, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|April 7, 2018
Beta-ketothiolase deficiency: An unusual cause of recurrent ketoacidosisGonca Kılıç-Yıldırım, Sultan Durmuş-Aydoğdu, Serdar Ceylaner, et al.
Brain & Development|December 24, 2014
Giant axonal disease: Report of eight casesFaruk Incecik, Ozlem M Herguner, Serdar Ceylaner, et al.
Clinics and Research in Hepatology and Gastroenterology|April 23, 2022
A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblingsKhaled Warasnhe, Figen Özçay, Halil İbrahim Aydin, et al.
The Journal of Obstetrics and Gynaecology Research|July 30, 2019
Analysis of TP53 gene in uterine myomas: No mutations but P72R polymorphism is associated with myoma developmentS Ozlem Altinkaya, Sumeyra N Avcioglu, Selda D Sezer, et al.
Anatolian Journal of Cardiology|December 20, 2017
A novel mutation in the desmoplakin gene in two female siblings with a rare form of dilated cardiomyopathy: Carvajal syndromeMehmet Gökhan Ramoğlu, Tayfun Uçar, Serdar Ceylaner, et al.
Archives of Gynecology and Obstetrics|April 5, 2007
Neu-Laxova syndrome, grossly appearing normal on 20 weeks ultrasonographic scan, that manifested late in pregnancy: a case reportSerkan Kahyaoglu, Inci Turgay, Ibrahim E Ertas, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 9, 2006
A case of fetal anticonvulsant syndrome with severe bilateral upper limb defectMelih Atahan Guven, Cem Batukan, Serdar Ceylaner, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Vici syndrome in siblings born to consanguineous parentsSener Tasdemir, Ibrahim Sahin, Atilla Cayır, et al.
Acta Neurologica Belgica|April 29, 2023
Could miglustat be a potential candidate in the treatment of action myoclonus renal failure syndrome?Seyda Erdoğan, Gül Yalçın Çakmaklı, Bülent Elibol, et al.
Pageof 25