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Showing articles 0 to 8 of 8 Filter Applied: lipid storage disorder of CNS (Click to remove) 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 Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis) NEJM 370:1830-1841, Case 14-2014, 2014 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Niemann-Pick Disease Type C: Two Cases and an Update Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000 Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C Neurol 45:1739-1743, Shulman,L.M.,et al, 1995 GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families Hum Genet 70:347-354, Giugliani,R.,et al, 1985 Clinicopathological Conference Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984 Adult Type Neuronal Storage Disease with Neuraminidase Deficiency Ann Neurol 6:232-244, Miyatake,T.,et al, 1979 Showing articles 0 to 8 of 8