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Journal Abstract Search

144 related items for PubMed ID: 5972561

  • 1. Tay-Sachs disease. A generalized metabolic disorder.
    Eeg-Olofsson L, Kristensson K, Sourander P, Svennerholm L.
    Acta Paediatr Scand; 1966 Nov; 55(6):546-62. PubMed ID: 5972561
    [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
    [No Abstract] [Full Text] [Related]

  • 3. Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.
    Derry DM, Fawcett JS, Andermann F, Wolfe LS.
    Neurology; 1968 Apr; 18(4):340-8. PubMed ID: 4173446
    [No Abstract] [Full Text] [Related]

  • 4. [Biochemical study of cerebral and hepatic lipids in a case of Tay-Sachs disease].
    Grégoire PE, Jonniaux G, Loeb H, Voet W, Capelle R.
    Rev Fr Etud Clin Biol; 1969 Apr; 14(6):568-74. PubMed ID: 5824260
    [No Abstract] [Full Text] [Related]

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  • 7. Electron histochemical demonstration of gangliosides in normal and Tay-Sachs brain tissue.
    Halaris A, Jatzkewitz H.
    Acta Neuropathol; 1969 Apr; 13(2):157-68. PubMed ID: 4185163
    [No Abstract] [Full Text] [Related]

  • 8. [Splenic and hepatic gangliosides in amaurotic idiocy of the Tay-Sachs type].
    Borri PF, Hooghwinkel GJ.
    Riv Neurobiol; 1967 Apr; 13(1):207-15. PubMed ID: 5602735
    [No Abstract] [Full Text] [Related]

  • 9. Vascular and pineal body involvement in juvenile amaurotic idiocy (Batten's disease).
    Perboll O.
    Acta Neuropathol; 1967 May; 8(2):210-4. PubMed ID: 6033099
    [No Abstract] [Full Text] [Related]

  • 10. Juvenile GM2-gangliosidosis. Clinical variant of Tay-Sachs disease or a new disease.
    Suzuki K, Rapin I, Suzuki Y, Ishii N.
    Neurology; 1970 Feb; 20(2):190-204. PubMed ID: 5460705
    [No Abstract] [Full Text] [Related]

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  • 12. [Tay-Sachs disease with hexosaminidase deficiency. Clinical, morphological and biochemical findings in a case with visceral storage of renal globosides].
    Pilz H, Müller D, Sandhoff K, ter Meulen V.
    Dtsch Med Wochenschr; 1968 Sep 27; 93(39):1833-9 passim. PubMed ID: 5679107
    [No Abstract] [Full Text] [Related]

  • 13. [An infantile-juvenile, subchronically progressive lipoidosis of the sphingomyelinoses (Niemann-Pick) form--a new type? Clinical, pathohistological, electron microscopic and biochemical studies].
    Wiedemann HR, Debuch H, Lennert K, Caesar R, Blümcke S, Harms D, Tolksdorf M, Seng PN, Korenke HD, Gerken H, Freitag F, Dörner K.
    Z Kinderheilkd; 1972 Sep 27; 112(3):187-225. PubMed ID: 5047097
    [No Abstract] [Full Text] [Related]

  • 14. Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.
    Brunngraber EG, Witting LA, Haberland C, Brown B.
    Brain Res; 1972 Mar 10; 38(1):151-62. PubMed ID: 4259417
    [No Abstract] [Full Text] [Related]

  • 15. Unusual forms of gangliosidoses involving the brain and viscera.
    Cumings JN, Dayan AD, Aitken JM, Guy J, Lewis GM.
    J Neurol Sci; 1971 Jun 10; 13(2):137-48. PubMed ID: 5579628
    [No Abstract] [Full Text] [Related]

  • 16. 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 10; 25(1):14-22. PubMed ID: 5146406
    [No Abstract] [Full Text] [Related]

  • 17. A case of late infantile systemic lipidosis.
    Suzuki K, Chen G.
    J Neuropathol Exp Neurol; 1967 Jan 10; 26(1):176. PubMed ID: 6022161
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  • 19. An autopsy case of Sandhoff's disease.
    Takahashi A, Saito K, Koizumi Y.
    Beitr Pathol; 1974 Sep 10; 152(4):418-28. PubMed ID: 4138910
    [No Abstract] [Full Text] [Related]

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