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Journal of Child Neurology|March 29, 2006
Central core disease: atypical case with respiratory insufficiency in an intensive care unitMuzaffer Polat, Ayse Tosun, Yilmaz Ay, et al.Pediatric Neurology|November 3, 2004
Value of biochemical markers for outcome in term infants with asphyxiaHasan Tekgul, Mehmet Yalaz, Necil Kutukculer, et al.Journal of Child Neurology|March 23, 2006
Vigabatrin caused rapidly progressive deterioration in two cases with early myoclonic encephalopathy associated with nonketotic hyperglycinemiaHasan Tekgul, Gul Serdaroğlu, Bulent Karapinar, et al.Pediatric Neurology|October 13, 2009
Neuropsychologic impairment in children with rolandic epilepsyYilmaz Ay, Sarenur Gokben, Gül Serdaroglu, et al.Brain & Development|July 2, 2015
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorderSanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 27, 2020
A transcranial magnetic stimulation study for the investigation of corticospinal motor pathways in children with cerebral palsyHasan Tekgul, Ulas Saz, Sanem Yilmaz, et al.Pediatric Neurology|July 4, 2006
Electrodiagnostic pattern approach for childhood polyneuropathiesMuzaffer Polat, Hasan Tekgul, Ahmet Kilincer, et al.Acta Neurologica Belgica|November 24, 2020
Clinical spectrum, treatment and outcome of myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease in children: a tertiary care experienceHepsen Mine Serin, Sanem Yilmaz, Erdem Simsek, et al.Seizure|January 4, 2011
Convulsive status epilepticus in children: etiology, treatment protocol and outcomeEylem Ulas Saz, Bulent Karapinar, Mustafa Ozcetin, et al.Metabolic Brain Disease|March 11, 2017
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencySanem Yilmaz, Mine Serin, Ebru Canda, et al.Pageof 5