These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Macular cherry-red spot, corneal clouding, and beta-galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease. Goldberg MF; Cotlier E; Fichenscher LG; Kenyon K; Enat R; Borowsky SA Arch Intern Med; 1971 Sep; 128(3):387-98. PubMed ID: 4999185 [No Abstract] [Full Text] [Related]
4. Beta-galactosidase deficiency in GM1 gangliosidosis of Friesian calves. Donnelly WJ; Sheahan BJ; Kelly M Res Vet Sci; 1973 Jul; 15(1):139-41. PubMed ID: 4778483 [No Abstract] [Full Text] [Related]
5. GM1 gangliosidosis type II. Hooft C; Vlietinck RF; Dacremont G; Kint JA Eur Neurol; 1970; 4(1):1-21. PubMed ID: 5473215 [No Abstract] [Full Text] [Related]
6. Beta-galactosidase activity in fibroblasts and tissues from sheep with a lysosomal storage disease. Ahern-Rindell AJ; Murnane RD; Prieur DJ Biochem Genet; 1988 Dec; 26(11-12):733-46. PubMed ID: 3149466 [TBL] [Abstract][Full Text] [Related]
7. Immunoelectron microscopical localization of lysosomal beta-galactosidase and its precursor forms in normal and mutant human fibroblasts. Willemsen R; Hoogeveen AT; Sips HJ; van Dongen JM; Galjaard H Eur J Cell Biol; 1986 Mar; 40(1):9-15. PubMed ID: 3084261 [TBL] [Abstract][Full Text] [Related]
8. Current concepts in genetics. Lysosomal storage diseases. Kolodny EH N Engl J Med; 1976 May; 294(22):1217-20. PubMed ID: 817200 [No Abstract] [Full Text] [Related]
9. [A case of adult type galactosialidosis--with special reference to pharmacologic and neurophysiologic studies on myoclonus]. Yarita H; Kurashina T; Sugano J; Murata K; Fukuda M Rinsho Shinkeigaku; 1988 Nov; 28(11):1234-40. PubMed ID: 3148380 [No Abstract] [Full Text] [Related]
16. [Lactose malabsorption and its ethnic influence in healthy Chinese]. Zheng JJ; Wang YM; Gong ZL Zhonghua Nei Ke Za Zhi; 1987 Mar; 26(3):135-7, 189. PubMed ID: 3113854 [No Abstract] [Full Text] [Related]
17. Editorial: The use of tears for heterozygote detection and genetic counseling. Goldberg MF Invest Ophthalmol; 1974 Mar; 13(3):159-60. PubMed ID: 4205146 [No Abstract] [Full Text] [Related]
18. [Skin and conjunctival biopsies in adult type beta-galactosidase neuraminidase deficiency]. Mori H; Hayashi A; Sato T Rinsho Shinkeigaku; 1985 Jul; 25(7):776-83. PubMed ID: 3935352 [No Abstract] [Full Text] [Related]
19. A family with beta-galactosidase deficiency: three adults with atypical clinical patterns. Mutoh T; Sobue I; Naoi M; Matsuoka Y; Kiuchi K; Sugimura K Neurology; 1986 Jan; 36(1):54-9. PubMed ID: 3079894 [TBL] [Abstract][Full Text] [Related]
20. An electrophoretic variant of beta-galactosidase with altered catalytic properties in a patient with GM1 gangliosidosis. Norden AG; O'Brien JS Proc Natl Acad Sci U S A; 1975 Jan; 72(1):240-4. PubMed ID: 804170 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]