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Showing articles 0 to 8 of 8 Filter Applied: developmental retardation (Click to remove) The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 A Middle-aged Woman with Severe Scoliosis and Encephalopathy JAMA Neurol 78:251-252, Mohan, G.,et al, 2021 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 Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest Radiology 182:493-499, Barkovich,A.J.&Kjos,B.O., 1992 Rett Syndrome:Natural History and Management Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988 Showing articles 0 to 8 of 8