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Case Reports in Genetics|July 23, 2014
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan geneGulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, 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.Pediatric Neurology|July 4, 2006
Electrodiagnostic pattern approach for childhood polyneuropathiesMuzaffer Polat, Hasan Tekgul, Ahmet Kilincer, et al.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.Seizure|January 4, 2011
Convulsive status epilepticus in children: etiology, treatment protocol and outcomeEylem Ulas Saz, Bulent Karapinar, Mustafa Ozcetin, et al.Pediatric Neurology|May 7, 2005
T-cell subsets and interleukin-6 response in Rasmussen's encephalitisHasan Tekgul, Muzaffer Polat, Omer Kitis, 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.Orphanet Journal of Rare Diseases|June 25, 2011
Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineationMarianne Rohrbach, Anthony Vandersteen, Uluç Yiş, et al.Pageof 4