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22. Oligosaccharide storage in brains from patients with fucosidosis, GM1-gangliosidosis and GM2-gangliosidosis (Sandhoff's disease). Tsay GC; Dawson G J Neurochem; 1976 Sep; 27(3):733-40. PubMed ID: 823301 [No Abstract] [Full Text] [Related]
23. [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]
24. Neuronal-visceral GM1 gangliosidosis in a dog with beta-galactosidase deficiency. Read DH; Harrington DD; Keenana TW; Hinsman EJ Science; 1976 Oct; 194(4263):442-5. PubMed ID: 824730 [TBL] [Abstract][Full Text] [Related]
25. Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders. Mueller OT; Henry WM; Haley LL; Byers MG; Eddy RL; Shows TB Proc Natl Acad Sci U S A; 1986 Mar; 83(6):1817-21. PubMed ID: 3081902 [TBL] [Abstract][Full Text] [Related]
27. [Disorders of mucopolysaccharide and glycoprotein metabolism]. Suzuki Y Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1304-10. PubMed ID: 2113302 [No Abstract] [Full Text] [Related]
28. Enhanced proteolytic degradation of normal beta-galactosidase in the lysosomal storage disease with combined beta-galactosidase and neuraminidase deficiency. van Diggelen OP; Hoogeveen AT; Smith PJ; Reuser AJ; Galjaard H Biochim Biophys Acta; 1982 Apr; 703(1):69-76. PubMed ID: 6803839 [No Abstract] [Full Text] [Related]
29. [A case of galactosialidosis discovered with external strabismus and cherry red spots in late infancy]. Tada H; Miyake S; Yamada M; Iwamoto H; Sakuraba H No To Hattatsu; 1988 Jan; 20(1):69-73. PubMed ID: 3126788 [No Abstract] [Full Text] [Related]
30. The biochemistry of sphingolipid storage diseases. Sandhoff K Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814 [No Abstract] [Full Text] [Related]
31. Hexosaminidases and ganglioside catabolism in the GM2-gangliosidoses. Tallman JF Chem Phys Lipids; 1974 Dec; 13(4):292-304. PubMed ID: 4615840 [No Abstract] [Full Text] [Related]
32. Postnatal development of glycosidases and gangliosides in the rat central nervous system. Prasad VV Int J Dev Neurosci; 1996 Jul; 14(4):481-7. PubMed ID: 8884381 [TBL] [Abstract][Full Text] [Related]
33. A case of GM1-gangliosidosis type I: glycosphingolipid profiles of urine and transformed lymphocytes and beta-D-galactosidase activities in peripheral lymphocytes, cultured skin fibroblasts and transformed lymphocytes. Asano K; Shindo N; Nakasuji M; Inamori K; Ohta M; Matsushita T; Yamaguchi M; Oshima M Jpn J Exp Med; 1990 Apr; 60(2):73-9. PubMed ID: 2117086 [TBL] [Abstract][Full Text] [Related]
34. [Two adult patients with GM1 ganglioside beta-galactosidase deficiency, showing myoclonus without radiological bony abnormalities]. Mutoh T; Matsuoka Y; Naoi M; Kiuchi K; Sobue I Rinsho Shinkeigaku; 1985 Mar; 25(3):321-35. PubMed ID: 3926367 [No Abstract] [Full Text] [Related]
36. 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]
37. Inherited lysosomal storage disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase in sheep. Ahern-Rindell AJ; Prieur DJ; Murnane RD; Raghavan SS; Daniel PF; McCluer RH; Walkley SU; Parish SM Am J Med Genet; 1988 Sep; 31(1):39-56. PubMed ID: 3146925 [TBL] [Abstract][Full Text] [Related]