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Showing articles 0 to 9 of 9 Filter Applied: developmental retardation (Click to remove) A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever Neurol 102:e209358, Barbosa,A.R.,et al, 2024 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Sturge-Weber Syndrome UptoDate , Nov, Bodensteiner, J.B., 2014 Sturge-Weber Syndrome MedLink Neurology, July, Comi, A.M., 2013 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ Ann Neurol 34:25-31, Koo,B.,et al, 1993 Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest Radiology 182:493-499, Barkovich,A.J.&Kjos,B.O., 1992 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Showing articles 0 to 9 of 9