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Showing articles 0 to 13 of 13 Filter Applied: developmental retardation (Click to remove) A Middle-aged Woman with Severe Scoliosis and Encephalopathy JAMA Neurol 78:251-252, Mohan, G.,et al, 2021 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease J Pediatr 123:242-247, Kelly,D.A.,et al, 1993 Infantile CNS Spongy Degeneration-14 Cases:Clinical Update Neurol 40:1876-1882, Gascon,G.G.,et al, 1990 Rett Syndrome:Natural History and Management Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988 Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome Ann Neurol 18:560-566, Belman,A.L.,et al, 1985 Alexander's Disease, A Disease of Astrocytes Brain 108:367-385, Borrett,D.&Becker,L.E., 1985 Santavuori Disease:Diagnosis by Leukocyte Ultrastructure Neurol 32:1277-1281, Baumann,R.J.,et al, 1982 Showing articles 0 to 13 of 13