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2. 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]
3. An enzymological approach to the lipidoses. Tallman JF; Pentchev PG; Brady RO Enzyme; 1974; 18(1):136-49. PubMed ID: 4211795 [No Abstract] [Full Text] [Related]
8. [Enzymatic diagnosis of glycolipidosis]. Zambotti V; Di Donato S; Rimoldi M; Tettamanti G Quad Sclavo Diagn; 1972 Mar; 8(1):183-98. PubMed ID: 4351703 [No Abstract] [Full Text] [Related]
9. A new type of mucolipidosis with -galactosidase deficiency and glycopeptiduria. Orii T; Minami R; Sukegawa K; Sato S; Tsugawa S Tohoku J Exp Med; 1972 Aug; 107(4):303-15. PubMed ID: 4264413 [No Abstract] [Full Text] [Related]
10. Sphingolipid hydrolases in brain tissue of patients with generalized gangliodosis. Brady RO; O'Brien JS; Bradley RM; Gal AE Biochim Biophys Acta; 1970 Jun; 210(1):193-5. PubMed ID: 5460531 [No Abstract] [Full Text] [Related]
11. The cerebral sphingolipidoses (metachromatic leucodystrophy and infantile amaurotic idiocy) as human inborn errors of metabolism. Jatzkewitz H Biochem J; 1972 Jun; 128(1):6P. PubMed ID: 5085660 [No Abstract] [Full Text] [Related]
18. Role of lysosomal acid ceramidase in the metabolism of ceramide in human skin fibroblasts. Chen WW; Moser AB; Moser HW Arch Biochem Biophys; 1981 May; 208(2):444-55. PubMed ID: 7259198 [No Abstract] [Full Text] [Related]
19. [Enzyme defects of fat metabolism]. Sailer S; Sandhofer F Wien Klin Wochenschr; 1971 Sep; 83(35):623-4. PubMed ID: 4109072 [No Abstract] [Full Text] [Related]