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Pediatric Neurology|September 13, 2011
Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopiaMaria Descartes, Fady M Mikhail, Judith C Franklin, et al.Pediatric Neurology|January 1, 1990
Ultrasonography, CT, and MRI of muscles in congenital nemaline myopathyC Wallgren-Pettersson, L Kivisaari, J Jääskeläinen, et al.Pediatric Neurology|January 1, 1990
Mosaic pattern of dystrophins in Duchenne muscular dystrophyN Tachi, K Sasaki, T Yamada, et al.Pediatric Neurology|August 10, 2011
Laterality of brain and ocular lesions in Aicardi syndromeMichelle T Cabrera, Bryan J Winn, Travis Porco, et al.Pediatric Neurology|August 10, 2011
Thyroid hormone levels in children receiving carbamazepine or valproateAnju Aggarwal, Neha Rastogi, Hema Mittal, et al.Pediatric Neurology|August 10, 2011
Quality of life in children and adolescents with cerebral palsy and myelomeningoceleBożena Okurowska-Zawada, Wojciech Kułak, Dorota Otapowicz, et al.Pediatric Neurology|August 10, 2011
Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutationSawako Yamazaki, Kanju Ikeno, Tokinari Abe, et al.Pediatric Neurology|August 10, 2011
MRI findings and steroid therapy for neuralgic amyotrophy in childrenKeitaro Yamada, Toshiyuki Mano, Yasuhisa Toribe, et al.Pediatric Neurology|February 23, 2012
Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencingHalil Dündar, Rıza Köksal Ozgül, Dilek Yalnızoğlu, et al.Pageof 597