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Journal Abstract Search

140 related items for PubMed ID: 4243740

  • 1. GM1-gangliosidosis without chondrodystrophy or visceromegaly. B-galactosidase deficiency with gangliosidosis and the excessive excretion of a keratan sulfate.
    Wolfe LS, Callahan J, Fawcett JS, Andermann F, Scriver CR.
    Neurology; 1970 Jan; 20(1):23-44. PubMed ID: 4243740
    [No Abstract] [Full Text] [Related]

  • 2. Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study.
    Patton VM, Dekaban AS.
    Arch Neurol; 1971 Jun; 24(6):529-37. PubMed ID: 5089899
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  • 7. An improved method for the detection of beta-galactosidase activity, and its application to G MI-gangliosidosis and mucopolysaccharidosis.
    Lake BD.
    Histochem J; 1974 Mar; 6(2):211-8. PubMed ID: 4275170
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  • 9. GM1 gangliosidosis type II.
    Hooft C, Vlietinck RF, Dacremont G, Kint JA.
    Eur Neurol; 1970 Mar; 4(1):1-21. PubMed ID: 5473215
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  • 12. Generalized gangliosidosis.
    Howell RR, Lippman EE.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):242-3. PubMed ID: 4281673
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  • 13. Impaired degradation of keratan sulfate in GM1-gangliosidosis.
    Yutaka T, Okada S, Kato T, Yabuuchi H.
    Clin Chim Acta; 1982 Oct 27; 125(2):233-40. PubMed ID: 6216030
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  • 15. Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease.
    Menkes JH, O'Brien JS, Okada S, Grippo J, Andrews JM, Cancilla PA.
    Arch Neurol; 1971 Jul 27; 25(1):14-22. PubMed ID: 5146406
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  • 16. Structure of the glycopeptide storage material in GM 1 gangliosidosis. Sequence determination with specific endo- and exoglycosidases.
    Tsay GC, Dawson G, Li Y-T.
    Biochim Biophys Acta; 1975 Apr 07; 385(2):305-11. PubMed ID: 1092358
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  • 17. [Clinical, pathological, and biochemical studies in a case of infantile generalized gangliosidosis (G M1 -mucolipidosis]].
    Pfeiffer RA, Diekmann L, Wierich W, von Bassewitz DB, Jünemann G, Damaske E, Werries E, Wässle K.
    Z Kinderheilkd; 1972 Apr 07; 112(1):23-42. PubMed ID: 4259738
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  • 18. Immunological studies of beta galactosidase in normal human liver and in GM1 gangliosidosis.
    Meisler M, Rattazzi MC.
    Am J Hum Genet; 1974 Nov 07; 26(6):683-91. PubMed ID: 4216265
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  • 19. Morquio B syndrome: a primary defect in beta-galactosidase.
    van der Horst GT, Kleijer WJ, Hoogeveen AT, Huijmans JG, Blom W, van Diggelen OP.
    Am J Med Genet; 1983 Oct 07; 16(2):261-75. PubMed ID: 6418007
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