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Journal Abstract Search
97 related items for PubMed ID: 817756
1. [An unusual form of amaurotic idiocy in infancy: Sandhoff's disease of GM 2 type 2 gangliosidosis]. Cordier J, Grignon G, Vidailhet M, Raspiller A. Bull Mem Soc Fr Ophtalmol; 1976; (87):238-42. PubMed ID: 817756 [No Abstract] [Full Text] [Related]
11. The pathology of Sandhoff's disease. Hadfield MG, Mamunes P, David RB. J Pathol; 1977 Nov; 123(3):137-44. PubMed ID: 592019 [Abstract] [Full Text] [Related]
12. [GM2 activator protein deficiency (AB variant form of GM2 gangliosidosis)]. Kondoh K, Sano A. Ryoikibetsu Shokogun Shirizu; 1998 Nov; (19 Pt 2):411-3. PubMed ID: 9645095 [No Abstract] [Full Text] [Related]
13. Glycolipid abnormalities in a myoclonic variant of late infantile amaurotic idiocy. Bartsch GG. J Lipid Res; 1970 May; 11(3):241-7. PubMed ID: 5441250 [Abstract] [Full Text] [Related]
14. A case of late infantile amaurotic idiocy and a case of an unusual storage disease with visceral involvement. Allegranza A, Strada GP, Borri PF. Pathol Eur; 1968 May; 3(2):248-58. PubMed ID: 5688461 [No Abstract] [Full Text] [Related]
15. Canine GM2-gangliosidosis: chemical and enzymatic features. Eto Y, Autilio-Gambetti L, McGrath JT. Adv Exp Med Biol; 1984 May; 174():431-40. PubMed ID: 6234761 [Abstract] [Full Text] [Related]
16. [Landing's disease or early infantile amaurotic idiocy with generalized gangliosidosis of the GM 1 type]. Sacrez R, Juif JG, Gigonnet JM, Gruner JE. Pediatrie; 1967 Mar; 22(2):143-62. PubMed ID: 4973280 [No Abstract] [Full Text] [Related]
17. A new variant of type-AB GM2-gangliosidosis. Li SC, Hirabayashi Y, Li YT. Biochem Biophys Res Commun; 1981 Jul 30; 101(2):479-85. PubMed ID: 7306091 [No Abstract] [Full Text] [Related]
18. Internalization of exogenous gangliosides in cultured skin fibroblasts for the diagnosis of mucolipidosis IV. Zeigler M, Bach G. Clin Chim Acta; 1986 Jun 15; 157(2):183-9. PubMed ID: 3087662 [Abstract] [Full Text] [Related]
19. Cerebral lipids in amaurotic idiocy. Wender M, Adamczewska Z, Dymecki J, Kulczycki J. Neuropatol Pol; 1971 Jun 15; 9(3):189-99. PubMed ID: 5111502 [No Abstract] [Full Text] [Related]
20. GM1 gangliosidosis: phenotypic variation in a single family. Farrell DF, Ochs U. Ann Neurol; 1981 Mar 15; 9(3):225-31. PubMed ID: 6784662 [Abstract] [Full Text] [Related] Page: [Next] [New Search]