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Serdar Ceylaner

Showing results (181-190 of 244) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 2, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3)Hacer Durmus, Elif Mertoğlu, Heinrich Sticht, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 8, 2015
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavinOzden O Horoz, Neslihan O Mungan, Dincer Yildizdas, et al.
Metabolic Brain Disease|April 1, 2021
Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemiaHarun Bayrak, Yılmaz Yıldız, Asburçe Olgaç, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2019
Mild hypotonia and recurrent seizures in an 8-month-old boy: AnswersSare Gülfem Özlü, Cigdem Seher Kasapkara, Serdar Ceylaner, et al.
Metabolic Brain Disease|July 2, 2018
Recurrent hepatic failure and status epilepticus: an uncommon presentation of hyperargininemiaHusniye Yucel, Çiğdem Seher Kasapkara, Meltem Akcaboy, et al.
Metabolic Brain Disease|April 16, 2018
Four Gaucher disease type II patients with three novel mutations: a single centre experience from TurkeyFatma Derya Bulut, Deniz Kör, Berna Şeker-Yılmaz, et al.
Turk Pediatri Arsivi|June 21, 2019
A rare structural myopathy: Nemaline myopathyOsman Yeşilbaş, Esra Şevketoğlu, Hasan Serdar Kıhtır, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2019
Mild hypotonia and recurrent seizures in an 8-month-old boy: QuestionsSare Gülfem Özlü, Cigdem Seher Kasapkara, Serdar Ceylaner, et al.
Turkish Archives of Pediatrics|September 22, 2023
Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?Gökcan Öztürk, Şule Haskoloğlu, Nazlı Deveci, et al.
The Turkish Journal of Pediatrics|January 10, 2020
Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutationsDeniz Kör, Berna Şeker-Yılmaz, Fatma Derya Bulut, et al.
Pageof 25

Showing results (181-190 of 244) with videos related to

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Pageof 25
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 2, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3)Hacer Durmus, Elif Mertoğlu, Heinrich Sticht, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 8, 2015
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavinOzden O Horoz, Neslihan O Mungan, Dincer Yildizdas, et al.
Metabolic Brain Disease|April 1, 2021
Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemiaHarun Bayrak, Yılmaz Yıldız, Asburçe Olgaç, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2019
Mild hypotonia and recurrent seizures in an 8-month-old boy: AnswersSare Gülfem Özlü, Cigdem Seher Kasapkara, Serdar Ceylaner, et al.
Metabolic Brain Disease|July 2, 2018
Recurrent hepatic failure and status epilepticus: an uncommon presentation of hyperargininemiaHusniye Yucel, Çiğdem Seher Kasapkara, Meltem Akcaboy, et al.
Metabolic Brain Disease|April 16, 2018
Four Gaucher disease type II patients with three novel mutations: a single centre experience from TurkeyFatma Derya Bulut, Deniz Kör, Berna Şeker-Yılmaz, et al.
Turk Pediatri Arsivi|June 21, 2019
A rare structural myopathy: Nemaline myopathyOsman Yeşilbaş, Esra Şevketoğlu, Hasan Serdar Kıhtır, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2019
Mild hypotonia and recurrent seizures in an 8-month-old boy: QuestionsSare Gülfem Özlü, Cigdem Seher Kasapkara, Serdar Ceylaner, et al.
Turkish Archives of Pediatrics|September 22, 2023
Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?Gökcan Öztürk, Şule Haskoloğlu, Nazlı Deveci, et al.
The Turkish Journal of Pediatrics|January 10, 2020
Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutationsDeniz Kör, Berna Şeker-Yılmaz, Fatma Derya Bulut, et al.
Pageof 25