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Annals of Indian Academy of Neurology|December 23, 2022
Botulinum Toxin Type A for the Treatment of Limb Myokymia: Experiences of Three ChildrenSedat Işıkay
Pediatric Neurology|March 25, 2014
Prevalence of celiac disease in children with idiopathic epilepsy in southeast TurkeySedat Işıkay, Halil Kocamaz
Journal of Pediatric Neurosciences|April 3, 2019
Congenital Muscular Dystrophy due to Novel Compound Heterozygote Mutations in POMGNT1 GeneSedat Işıkay, Akif Şirikçi
The Turkish Journal of Pediatrics|December 30, 2022
Evaluation of hair structural abnormalities in children with different neurological diseasesSüleyman Hilmi Sevinç, Sedat Işıkay
The Turkish Journal of Pediatrics|January 30, 2018
An infant with glutaric aciduria type IIc diagnosed with a novel mutationSedat Işıkay, Ayhan Yaman, Serdar Ceylaner
Journal of Clinical Research in Pediatric Endocrinology|March 8, 2012
Pseudohypoparathyroidism presenting with ventricular arrhythmia: a case reportSedat Işıkay, İlyas Akdemir, Kutluhan Yılmaz
Turkiye Parazitolojii Dergisi|March 28, 2012
[Two cases of rare cerebral hydatid cyst]Sedat Işıkay, Kutluhan Yılmaz, Akgün Ölmez
Iranian Journal of Pediatrics|March 21, 2015
A case of congenital disorder of glycosylation ia presented with recurrent pericardial effusionSedat Işıkay, Osman Başpınar, Kutluhan Yılmaz
The American Journal of Emergency Medicine|January 17, 2012
Neurobrucellosis developing unilateral oculomotor nerve paralysisSedat Işıkay, Kutluhan Yılmaz, Akgün Ölmez
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