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Showing articles 0 to 12 of 12 Filter Applied: lipid storage disorder of CNS (Click to remove) Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis) NEJM 370:1830-1841, Case 14-2014, 2014 Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease) Adams & Victors Principles of Neurology, Chp 37, pg 960, Ropper, A.H.,et al, 2014 Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009 Amaurotic Family Idiocy Am J Dis Child 142:53-56, Abt,I.A., 1988 Bone-Marrow Transplantation for Neurovisceral Storage Disorders Editorial, Lancet 2:788-7891986., , 1986 Enzyme Replacement in Nervous Tissue After Allogeneic Bone-Marrow Transplantation for Fucosidoisis in Dogs Lancet 2:772-774, Taylor,R.M.,et al, 1986 GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families Hum Genet 70:347-354, Giugliani,R.,et al, 1985 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Adult Type Neuronal Storage Disease with Neuraminidase Deficiency Ann Neurol 6:232-244, Miyatake,T.,et al, 1979 Chronic Hexosaminidase A & B Deficiency et al. , Ann Neurol 2:156977., Goldie,W.D., 1977 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Enzyme Replacement Therapy in Fabry Disease JAMA 285:2743-2749, Schiffmann,R.,et al, 2001 Showing articles 0 to 12 of 12