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Journal Abstract Search

151 related items for PubMed ID: 5581981

  • 1. Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.
    Okada S, Veath ML, Leroy J, O'Brien JS.
    Am J Hum Genet; 1971 Jan; 23(1):55-61. PubMed ID: 5581981
    [No Abstract] [Full Text] [Related]

  • 2. A case of GM2-gangliosidosis with total hexosaminidase deficiency.
    Suzuki Y, Jacob JC, Suzuki K, Suzuki K.
    Neurology; 1970 Apr; 20(4):388. PubMed ID: 5535009
    [No Abstract] [Full Text] [Related]

  • 3. Ganglioside storage diseases.
    O'Brien JS, Okada S, Ho MW, Fillerup DL, Veath ML, Adams K.
    Fed Proc; 1971 Apr; 30(3):956-69. PubMed ID: 4252532
    [No Abstract] [Full Text] [Related]

  • 4. Gm2-gangliosidosis: studies in cultured fibroblasts.
    Kolodny EH, Milunsky A, Sheng GS.
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):130-5. PubMed ID: 4611525
    [No Abstract] [Full Text] [Related]

  • 5. Partial deficiency of hexosaminidase component a in juvenile gm2-gangliosidosis.
    Suzuki Y, Suzuki K.
    Neurology; 1970 Sep; 20(9):848-51. PubMed ID: 5466454
    [No Abstract] [Full Text] [Related]

  • 6. Ganglioside-storage diseases.
    O'Brien JS.
    N Engl J Med; 1971 Apr 22; 284(15):893-6. PubMed ID: 5549832
    [No Abstract] [Full Text] [Related]

  • 7. Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A.
    Okada S, Veath ML, O'Brien JS.
    J Pediatr; 1970 Dec 22; 77(6):1063-5. PubMed ID: 5486623
    [No Abstract] [Full Text] [Related]

  • 8. Gm2-gangliosidosis with total hexosaminidase deficiency.
    Suzuki Y, Jacob JC, Suzuki K, Kutty KM, Suzuki K.
    Neurology; 1971 Apr 22; 21(4):313-28. PubMed ID: 4251893
    [No Abstract] [Full Text] [Related]

  • 9. Ganglioside storage diseases.
    O'Brien JS.
    Adv Hum Genet; 1972 Apr 22; 3():39-98. PubMed ID: 4268938
    [No Abstract] [Full Text] [Related]

  • 10. Hexosaminidases and ganglioside catabolism in the GM2-gangliosidoses.
    Tallman JF.
    Chem Phys Lipids; 1974 Dec 22; 13(4):292-304. PubMed ID: 4615840
    [No Abstract] [Full Text] [Related]

  • 11. Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts.
    Dawson G, Matalon R, Stein AO.
    J Pediatr; 1971 Sep 22; 79(3):423-9. PubMed ID: 5567965
    [No Abstract] [Full Text] [Related]

  • 12. 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 22; 25(1):14-22. PubMed ID: 5146406
    [No Abstract] [Full Text] [Related]

  • 13. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.
    Sandhoff K, Andreae U, Jatzkewitz H.
    Pathol Eur; 1968 Jul 22; 3(2):278-85. PubMed ID: 5688464
    [No Abstract] [Full Text] [Related]

  • 14. Metabolic diseases: more clues from enzymes.
    Nature; 1970 May 16; 226(5246):596. PubMed ID: 5444922
    [No Abstract] [Full Text] [Related]

  • 15. Tay-Sachs' retina. Deficiency of acetyl hexosaminidase A.
    Cotlier E.
    Arch Ophthalmol; 1971 Sep 16; 86(3):352-6. PubMed ID: 5095559
    [No Abstract] [Full Text] [Related]

  • 16. Hexosaminidase activities in a case of systemic GM2 gangliosidosis of late infantile type.
    Schneck L, Friedland J, Pourfar M, Saifer A, Volk BW.
    Proc Soc Exp Biol Med; 1970 Mar 16; 133(3):997-8. PubMed ID: 5435594
    [No Abstract] [Full Text] [Related]

  • 17. [Enzymatic diagnosis of glycolipidosis].
    Zambotti V, Di Donato S, Rimoldi M, Tettamanti G.
    Quad Sclavo Diagn; 1972 Mar 16; 8(1):183-98. PubMed ID: 4351703
    [No Abstract] [Full Text] [Related]

  • 18. Five gangliosidoses.
    O'Brien JS.
    Lancet; 1969 Oct 11; 2(7624):805. PubMed ID: 4186052
    [No Abstract] [Full Text] [Related]

  • 19. Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis.
    Sloan HR, Uhlendorf BW, Jacobson CB, Fredrickson DS.
    Pediatr Res; 1969 Nov 11; 3(6):532-7. PubMed ID: 5361691
    [No Abstract] [Full Text] [Related]

  • 20. Demonstration of an alteration of ganglioside metabolism in Tay-Sachs disease.
    Kolodny EH, Brady RO, Volk BW.
    Biochem Biophys Res Commun; 1969 Oct 22; 37(3):526-31. PubMed ID: 5388728
    [No Abstract] [Full Text] [Related]

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