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Pediatric Neurology|October 22, 2013
Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutationsMaina Kava, David Chitayat, Susan Blaser, et al.Pediatric Neurology|October 22, 2013
Successful clinical treatment of child stroke using mechanical embolectomySophie Dubedout, Christophe Cognard, Claude Cances, et al.Pediatric Neurology|October 22, 2013
Lambert-Eaton syndrome, an unrecognized treatable pediatric neuromuscular disorder: three patients and literature reviewMirna Hajjar, Jennifer Markowitz, Basil T Darras, et al.Pediatric Neurology|October 22, 2013
Cerebrospinal fluid TNF-α, IL-6, and IL-8 in children with bacterial meningitisRajniti Prasad, Rishi Kapoor, Ragini Srivastava, et al.Pediatric Neurology|October 22, 2013
Automatically quantified diffuse excessive high signal intensity on MRI predicts cognitive development in preterm infantsNehal A Parikh, Lili He, Eliana Bonfante-Mejia, et al.Pediatric Neurology|October 22, 2013
Cystathionine beta-synthase deficiency heralded by cerebral sinus venous thrombosis and strokeIlene S Ruhoy, J Lawrence Merritt, Catherine Amlie-LefondPediatric Neurology|November 9, 2013
A three-year-old boy with glucose transporter type 1 deficiency syndrome presenting with episodic ataxiaAkiko Ohshiro-Sasaki, Hiroko Shimbo, Kyoko Takano, et al.Pediatric Neurology|February 23, 2012
Risk factors for isolated periventricular leukomalaciaKhalil I Al Tawil, Heba S El Mahdy, Muhammad T Al Rifai, et al.Pediatric Neurology|February 23, 2012
Developmental coordination disorder: a pilot diffusion tensor imaging studyJill G Zwicker, Cheryl Missiuna, Susan R Harris, et al.Pediatric Neurology|February 23, 2012
Dual diagnosis of dihydropyrimidine dehydrogenase deficiency and GM₁ gangliosidosisMin T Ong, Gabriel C S Chow, Richard E MortonPageof 597