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PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 4276769

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  • 3. [Amaurotic familial idiocy within the scope of GM2-gangliosidosis. Apropos of a case of Sandhoff's disease studied on the clinical, neuropathological, enzymatic, and genetic levels].
    Mounoud RL.
    J Genet Hum; 1974 Jun; 22(2):139-83. PubMed ID: 4609324
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  • 5. Development and distribution of lysosomal enzymes and disaccharidases in human fetal intestine.
    Antonowicz I, Chang SK, Grand RJ.
    Gastroenterology; 1974 Jul; 67(1):51-8. PubMed ID: 4858137
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  • 8. [Significance and origin of lysosomal enzymes in the synovial fluid in chronic joint diseases].
    Eberhard A, Laas U, Vojtisek O, Greiling H.
    Z Rheumaforsch; 1972 Jul; 31(3):105-18. PubMed ID: 5027028
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  • 11. [GM2 gangliosidosis with total beta-N-acetyl-hexosaminidase deficit or Sandhoff's disease].
    Juif JG, Luckel JC, Nussbaum JL, Stoebner R, Kapps R.
    Arch Fr Pediatr; 1973 Jan; 30(1):29-43. PubMed ID: 4721586
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  • 14. GM3 (hematoside) sphingolipodystrophy.
    Max SR, Maclaren NK, Brady RO, Bradley RM, Rennels MB, Tanaka J, Garcia JH, Cornblath M.
    N Engl J Med; 1974 Oct 31; 291(18):929-31. PubMed ID: 4213132
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  • 17. Tay-Sachs' retina. Deficiency of acetyl hexosaminidase A.
    Cotlier E.
    Arch Ophthalmol; 1971 Sep 31; 86(3):352-6. PubMed ID: 5095559
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  • 18. Lysosomal enzyme variations in cultured normal skin fibroblasts.
    Milunsky A, Spielvogel C, Kanfer JN.
    Life Sci II; 1972 Nov 22; 11(22):1101-7. PubMed ID: 4663811
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