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Showing articles 0 to 12 of 12 Filter Applied: mental retardation (Click to remove) Arginase Deficiency Presenting as Cerebral Palsy Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 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 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Congenital Muscular Dystrophy J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989 Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration Neurol 37:446-450, Larsen,R.,et al, 1987 Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis Ann Neurol 20:89-91, Argov,Z.,et al, 1986 Neurological Manifestations in Xeroderma Pigmentosum Ann Neurol 20:70-75, Mimaki,T.,et al, 1986 Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Showing articles 0 to 12 of 12