Tay-sachs disease
- PMID: 5347842
- DOI: 10.1056/NEJM196911272812213
Tay-sachs disease
Similar articles
-
Demonstration of an alteration of ganglioside metabolism in Tay-Sachs disease.Biochem Biophys Res Commun. 1969 Oct 22;37(3):526-31. doi: 10.1016/0006-291x(69)90947-4. Biochem Biophys Res Commun. 1969. PMID: 5388728 No abstract available.
-
Further studies on the elucidation of the enzymatic defect in Tay-Sachs disease.Neurology. 1970 Apr;20(4):388. Neurology. 1970. PMID: 5535010 No abstract available.
-
Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.Pathol Eur. 1968;3(2):278-85. Pathol Eur. 1968. PMID: 5688464 No abstract available.
-
The enzymology of Tay-Sachs disease and its variant forms.UCLA Forum Med Sci. 1975;(18):479-99. doi: 10.1016/b978-0-12-139050-1.50035-5. UCLA Forum Med Sci. 1975. PMID: 812231 Review. No abstract available.
-
Disorders of ganglioside metabolism.Prog Med Genet. 1972;8:225-41. Prog Med Genet. 1972. PMID: 4336471 Review. No abstract available.
Cited by
-
Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases.West J Med. 1977 Jan;126(1):46-54. West J Med. 1977. PMID: 831367 Free PMC article. No abstract available.
-
The biochemical genetics of the hexosaminidase system in man.Am J Hum Genet. 1979 Mar;31(2):95-105. Am J Hum Genet. 1979. PMID: 377957 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources