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Showing articles 0 to 14 of 14 Filter Applied: developmental retardation (Click to remove) Duchenne Muscular Dystrophy BMJ 368:L7012, Fox, H.,et al, 2020 Case 35-2006: A Newborn Boy with Hypotonia NEJM 355:2132-2142, Brown,R.H.,et al, 2006 Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form Neurol 46:815-818, Kobayashi,O.,et al, 1996 Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining Neurol 46:810-814, Connolly,A.M.,et al, 1996 Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 Recognising & Preventing Duchenne Muscular Dystrophy BMJ 287:1083-1084, Firth,M.A.,et al, 1983 Diagnostic Delay in Duchenne's Muscular Dystrophy JAMA 247:478-480, Crisp,D.E.,et al, 1982 Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification Neurol 87:e56-e57, Saini, A.G.,et al, 2016 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 Joubert Syndrome:A Clinico-Radiological Study Neuroradiology 31:502-506, Kendall,B.,et al, 1990 Santavuori Disease:Diagnosis by Leukocyte Ultrastructure Neurol 32:1277-1281, Baumann,R.J.,et al, 1982 Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980 Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979 Showing articles 0 to 14 of 14