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PUBMED FOR HANDHELDS

Journal Abstract Search

139 related items for PubMed ID: 5473215

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  • 2. GM1-ganglioside accumulation and beta-galactosidase deficiency in a case of GM1-gangliosidosis (Landing disease).
    Dacremont G, Kint JA.
    Clin Chim Acta; 1968 Sep; 21(3):421-5. PubMed ID: 5725200
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  • 8. Leukocyte beta-galactosidase activity in the diagnosis of generalized GM 1 gangliosidosis.
    Singer HS, Nankervis GA, Schafer IA.
    Pediatrics; 1972 Mar; 49(3):352-61. PubMed ID: 4258708
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  • 9. Partial deficiency of hexosaminidase component a in juvenile gm2-gangliosidosis.
    Suzuki Y, Suzuki K.
    Neurology; 1970 Sep; 20(9):848-51. PubMed ID: 5466454
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  • 10. 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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  • 11. 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
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  • 14. Editorial: The use of tears for heterozygote detection and genetic counseling.
    Goldberg MF.
    Invest Ophthalmol; 1974 Mar; 13(3):159-60. PubMed ID: 4205146
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  • 15. Generalized gangliosidosis: beta-galactosidase deficiency.
    Okada S, O'Brien JS.
    Science; 1968 May 31; 160(3831):1002-4. PubMed ID: 5647842
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  • 18. GM1 gangliosidosis type I.
    Weiss MJ, Krill AE, Dawson G, Hindman J, Cotlier E.
    Am J Ophthalmol; 1973 Dec 31; 76(6):999-1004. PubMed ID: 4759862
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