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Journal Abstract Search

146 related items for PubMed ID: 4276769

  • 21. Lysosomal enzymes in juvenile amaurotic idiocy.
    Ockerman PA.
    Acta Paediatr Scand; 1968 Nov; 57(6):537-9. PubMed ID: 5706371
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  • 26. Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.
    Harzer K.
    Humangenetik; 1973 Nov; 20(1):9-24. PubMed ID: 4776531
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  • 27. Subcellular particles of human platelets. A biochemical and electron microscopic study with particular reference to the influence of fractionation techniques.
    Day HJ, Holmsen H, Hovig T.
    Scand J Haematol Suppl; 1969 Nov; 7():3-35. PubMed ID: 4310890
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  • 29. Enzymic differentiation between different types of Tay-Sachs disease of similar clinical appearance.
    Clausen J, Melchior JC, Paerregaard P.
    Eur Neurol; 1972 Nov; 7(1):56-64. PubMed ID: 4336274
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  • 34. [Enzymatic diagnosis of glycolipidosis].
    Zambotti V, Di Donato S, Rimoldi M, Tettamanti G.
    Quad Sclavo Diagn; 1972 Mar; 8(1):183-98. PubMed ID: 4351703
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  • 36. Urinary mannose in mannosidosis.
    Nordén NE, Ockerman PA, Szabó L.
    J Pediatr; 1973 Apr; 82(4):686-8. PubMed ID: 4633365
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  • 37. Separation of N-acetyl- -D-hexosaminamidase-isoenzymes from human brain and leukocytes by cellulose acetate paper electrophoresis: a simple procedure for the diagnosis of Tay-Sachs disease.
    Klibansky C.
    Isr J Med Sci; 1971 Sep; 7(9):1086-9. PubMed ID: 5151274
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