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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 IşıkayThe Turkish Journal of Pediatrics|January 30, 2018
The behavior pattern of parents of patients with subacute sclerosing panencephalitis concerning alternative medicineSedat IşıkayPediatric Neurology|March 25, 2014
Prevalence of celiac disease in children with idiopathic epilepsy in southeast TurkeySedat Işıkay, Halil KocamazJournal of Pediatric Neurosciences|April 3, 2019
Congenital Muscular Dystrophy due to Novel Compound Heterozygote Mutations in POMGNT1 GeneSedat Işıkay, Akif ŞirikçiThe Turkish Journal of Pediatrics|December 30, 2022
Evaluation of hair structural abnormalities in children with different neurological diseasesSüleyman Hilmi Sevinç, Sedat IşıkayThe Turkish Journal of Pediatrics|January 30, 2018
An infant with glutaric aciduria type IIc diagnosed with a novel mutationSedat Işıkay, Ayhan Yaman, Serdar CeylanerJournal of Clinical Research in Pediatric Endocrinology|March 8, 2012
Pseudohypoparathyroidism presenting with ventricular arrhythmia: a case reportSedat Işıkay, İlyas Akdemir, Kutluhan YılmazTurkiye Parazitolojii Dergisi|March 28, 2012
[Two cases of rare cerebral hydatid cyst]Sedat Işıkay, Kutluhan Yılmaz, Akgün ÖlmezIranian Journal of Pediatrics|March 21, 2015
A case of congenital disorder of glycosylation ia presented with recurrent pericardial effusionSedat Işıkay, Osman Başpınar, Kutluhan YılmazThe American Journal of Emergency Medicine|January 17, 2012
Neurobrucellosis developing unilateral oculomotor nerve paralysisSedat Işıkay, Kutluhan Yılmaz, Akgün ÖlmezPageof 2