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Showing articles 0 to 11 of 11 Filter Applied: developmental retardation (Click to remove) A Child with Arthrogryposis Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 A Child with Delayed Motor Milestones and Ptosis Neurol 88:e158-e163, Ghosh, P.S., 2017 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 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 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 Joubert Syndrome:A Clinico-Radiological Study Neuroradiology 31:502-506, Kendall,B.,et al, 1990 Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis Ann Neurol 18:614-617, Wolf,B.,et al, 1985 Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin NEJM 304:817-820, Thoene,J.,et al, 1981 Congenital Ocular Motor Apraxia Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979 Showing articles 0 to 11 of 11