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Showing articles 0 to 8 of 8 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 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Amaurotic Family Idiocy Am J Dis Child 142:53-56, Abt,I.A., 1988 The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985 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 Chronic Hexosaminidase A & B Deficiency et al. , Ann Neurol 2:156977., Goldie,W.D., 1977 Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes NEJM 289:1072, Carmody,P.,et al, 1973 Showing articles 0 to 8 of 8