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4. 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]
5. Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptoms. Hultberg B; Ockerman PA; Sjöblad S Eur Neurol; 1972; 7(1):101-18. PubMed ID: 4259742 [No Abstract] [Full Text] [Related]
6. [Generalized GM 1 gangliosidosis: ultrastructure and differential diagnostic importance of storage lymphocytes and bone marrow cells]. Heyne K; Kemmer C; Simon C; Trübsbach A Padiatr Padol; 1973; 8(3):272-83. PubMed ID: 4734063 [No Abstract] [Full Text] [Related]
8. [A case of thesaurismosis of the late amaurotic idiocy type]. Spadetta V; De Giacomo P; Borri P; Perniola T Acta Neurol (Napoli); 1969; 24(2):231-7. PubMed ID: 5386342 [No Abstract] [Full Text] [Related]
17. [GM1- and GM2-gangliosidosis. First cases in Finland]. Palo J; Haltia M; Amnell G Duodecim; 1975; 91(6):354-61. PubMed ID: 1140115 [No Abstract] [Full Text] [Related]
19. [The amaurotic idiocies: correlation between biochemical data and clinical courses]. Pilz H Dtsch Z Nervenheilkd; 1968; 194(3):187-218. PubMed ID: 5721984 [No Abstract] [Full Text] [Related]
20. [Lipids of the erythrocytes in the diagnosis in vivo of sphingolipidosis]. Hooghwinkel GJ; Borri P; Bertinelli RP; Paci A Acta Neurol (Napoli); 1970; 25(2):164-9. PubMed ID: 5422840 [No Abstract] [Full Text] [Related] [Next] [New Search]