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2. [Adult type galactosialidosis--alcohol and myoclonus]. Hashimoto K; Ugawa Y; Nakase H; Kunimoto M; Mannen T Rinsho Shinkeigaku; 1986 Sep; 26(9):941-7. PubMed ID: 3098487 [No Abstract] [Full Text] [Related]
3. [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]
4. Juvenile galactosialidosis in a white male: a new variant. Chitayat D; Applegarth DA; Lewis J; Dimmick JE; McCormick AQ; Hall JG Am J Med Genet; 1988 Dec; 31(4):887-901. PubMed ID: 3149149 [TBL] [Abstract][Full Text] [Related]
5. [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]
6. [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]
9. Galactosialidosis: a direct evidence that a 46-kilodalton protein restores deficient enzyme activities in fibroblasts. Nanba E; Tsuji A; Omura K; Suzuki Y Biochem Biophys Res Commun; 1987 Apr; 144(1):138-42. PubMed ID: 3107551 [TBL] [Abstract][Full Text] [Related]
10. Galactosialidosis: molecular heterogeneity in biosynthesis and processing of protective protein for beta-galactosidase. Nanba E; Tsuji A; Omura K; Suzuki Y Hum Genet; 1988 Dec; 80(4):329-32. PubMed ID: 3143661 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. The presence of a reduced amount of 32-kd "protective" protein is a distinct biochemical finding in late infantile galactosialidosis. Strisciuglio P; Parenti G; Giudice C; Lijoi S; Hoogeveen AT; d'Azzo A Hum Genet; 1988 Nov; 80(3):304-6. PubMed ID: 3142815 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes. Palmeri S; Hoogeveen AT; Verheijen FW; Galjaard H Am J Hum Genet; 1986 Feb; 38(2):137-48. PubMed ID: 3080874 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosis. Yoshino H; Miyashita K; Miyatani N; Ariga T; Hashimoto Y; Tsuji S; Oyanagi K; Ohama E; Ikuta F; Suzuki A J Neurol Sci; 1990 Jun; 97(1):53-65. PubMed ID: 2115076 [TBL] [Abstract][Full Text] [Related]
17. Involvement of thiol proteases in galactosialidosis. Takeda E; Kuroda Y; Toshima K; Naito E; Ito M; Miyao M; Kominami E; Katunuma N Clin Chim Acta; 1986 Mar; 155(2):109-15. PubMed ID: 3084137 [TBL] [Abstract][Full Text] [Related]