Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases
- PMID: 831367
- PMCID: PMC1237428
Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases
Similar articles
-
[Value of studying isoenzymes in hereditary lysosomal lipidoses. In particular beta-glucosidase (Gaucher's disease) and acid lipase (Wolman's disease and cholesterol ester storage disease)].Bull Acad Natl Med. 1985 Jan;169(1):58-65. Bull Acad Natl Med. 1985. PMID: 3926252 French. No abstract available.
-
Tay-Sachs and other lipid storage diseases.HSMHA Health Rep. 1971 Sep;86(9):769-74. HSMHA Health Rep. 1971. PMID: 4331588 Free PMC article. No abstract available.
-
Investigations in enzyme replacement therapy in lipid storage diseases.Fed Proc. 1975 Apr;34(5):1310-5. Fed Proc. 1975. PMID: 804420
-
[Tay-Sachs disease].Nihon Rinsho. 1973 Aug 10;31(8):2463-8. Nihon Rinsho. 1973. PMID: 4588056 Review. Japanese. No abstract available.
-
Gaucher's disease: advances and challenges.Adv Pediatr. 1989;36:277-306. Adv Pediatr. 1989. PMID: 2675571 Review. No abstract available.
Cited by
-
Alglucerase. A review of its therapeutic use in Gaucher's disease.Drugs. 1992 Jul;44(1):72-93. doi: 10.2165/00003495-199244010-00007. Drugs. 1992. PMID: 1379912 Review.
-
Skeletal involvement in Gaucher disease: extent of bone disease, splenic volume, and quality of life.Radiol Bras. 2021 Mar-Apr;54(2):71-76. doi: 10.1590/0100-3984.2020.0014. Radiol Bras. 2021. PMID: 33854259 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources