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2. A case of GM2-gangliosidosis with total hexosaminidase deficiency. Suzuki Y; Jacob JC; Suzuki K; Suzuki K Neurology; 1970 Apr; 20(4):388. PubMed ID: 5535009 [No Abstract] [Full Text] [Related]
3. Hexosaminidases and ganglioside catabolism in the GM2-gangliosidoses. Tallman JF Chem Phys Lipids; 1974 Dec; 13(4):292-304. PubMed ID: 4615840 [No Abstract] [Full Text] [Related]
7. Enzyme defects in the sphingolipidoses and their application to diagnosis. Brady RO Ann Clin Lab Sci (1971); 1972; 2(4):285-94. PubMed ID: 4342099 [No Abstract] [Full Text] [Related]
9. Beta-D-galactosidase in human urine: deficiency in generalized gangliosidosis. Thomas GH J Lab Clin Med; 1969 Nov; 74(5):725-31. PubMed ID: 5350201 [No Abstract] [Full Text] [Related]
10. G M2 gangliosidoses: consideration of the genetic defects. Tateson R; Bain AD Lancet; 1971 Sep; 2(7724):612-3. PubMed ID: 4106135 [No Abstract] [Full Text] [Related]
11. Multiple forms of glycosidases in the normal and pathological states. Robinson D Enzyme; 1974; 18(1):114-35. PubMed ID: 4277585 [No Abstract] [Full Text] [Related]
12. Biochemical expression of degenerative disorders associated with cognitive dysfunction. Wolfe LS Res Publ Assoc Res Nerv Ment Dis; 1979; 57():125-43. PubMed ID: 105384 [No Abstract] [Full Text] [Related]
13. Introductory remarks on ganglioside metabolism. Gatt S Adv Exp Med Biol; 1980; 125():209-12. PubMed ID: 6444773 [No Abstract] [Full Text] [Related]
14. [Heterogeneity of inborn glycolipidoses and glycoproteinoses and their enzymologic diagnosis]. Tsvetkova IV Vopr Med Khim; 1982; 28(3):32-41. PubMed ID: 6808764 [No Abstract] [Full Text] [Related]