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Journal Abstract Search

180 related items for PubMed ID: 4185163

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

  • 2.
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  • 4. Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis).
    Suzuki K, Chen GC.
    J Neuropathol Exp Neurol; 1968 Jan; 27(1):15-38. PubMed ID: 5656575
    [No Abstract] [Full Text] [Related]

  • 5. G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis.
    Volk BW, Adachi M, Schneck L, Saifer A, Kleinberg W.
    Arch Pathol; 1969 Apr; 87(4):393-403. PubMed ID: 5766766
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. GM-1 gangliosidosis in a cat.
    Blakemore WF.
    J Comp Pathol; 1972 Apr; 82(2):179-85. PubMed ID: 5040871
    [No Abstract] [Full Text] [Related]

  • 8. A type of juvenile cerebromacular degeneration characterized by granular osmiophilic deposits.
    Carpenter S, Karpati G, Wolfe LS, Andermann F.
    J Neurol Sci; 1973 Jan; 18(1):67-87. PubMed ID: 4120484
    [No Abstract] [Full Text] [Related]

  • 9. 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; 25(1):14-22. PubMed ID: 5146406
    [No Abstract] [Full Text] [Related]

  • 10. [Concerning brain gangliosides in Tay-Sachs disease].
    Wagner A.
    Klin Wochenschr; 1966 Apr 01; 44(7):398-402. PubMed ID: 5983851
    [No Abstract] [Full Text] [Related]

  • 11. [Splenic and hepatic gangliosides in amaurotic idiocy of the Tay-Sachs type].
    Borri PF, Hooghwinkel GJ.
    Riv Neurobiol; 1967 Apr 01; 13(1):207-15. PubMed ID: 5602735
    [No Abstract] [Full Text] [Related]

  • 12. Tay-sachs disease. Demonstration of the stored ganglioside in cultured cells from brain biopsy.
    Batzdorf U, Sarlieve LL, Gold VA, Menkes JH.
    Arch Neurol; 1969 Jun 01; 20(6):650-2. PubMed ID: 4890200
    [No Abstract] [Full Text] [Related]

  • 13. Abnormal gangliosides in Tay-Sachs disease, Niemann-Pick's disease, and gargoylism.
    Booth DA, Goodwin H, Cumings JN.
    J Lipid Res; 1966 May 01; 7(3):337-40. PubMed ID: 4959256
    [Abstract] [Full Text] [Related]

  • 14. [G-M2 gangliosidosis and other neuronal lipodystrophies in amaurosis in the dog. A comparative histopathological, histochemical, electron microscope and biochemical study].
    Karbe E.
    Arch Exp Veterinarmed; 1971 May 01; 25(1):1-48. PubMed ID: 4934546
    [No Abstract] [Full Text] [Related]

  • 15. [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 May 01; 14(6):568-74. PubMed ID: 5824260
    [No Abstract] [Full Text] [Related]

  • 16. Late infantile amaurotic idiocy (LIAI). Anatomochemical report of a case.
    Haberland C, Brunngraber EG, Witting LA, Hof H.
    Neurology; 1972 Mar 01; 22(3):305-11. PubMed ID: 5062265
    [No Abstract] [Full Text] [Related]

  • 17. FORMATION OF THE MEMBRANOUS CYTOPLASMIC BODIES IN TAY-SACHS DISEASE: AN IN VITRO STUDY.
    SAMUELS S, GONATAS NK, WEISS M.
    J Neuropathol Exp Neurol; 1965 Apr 01; 24():256-64. PubMed ID: 14280501
    [No Abstract] [Full Text] [Related]

  • 18. [Sphingosine bases of the gangliosides accumulated in 2 variants of infantile amaurotic idiocy].
    Klenk E, Naoi M.
    Hoppe Seylers Z Physiol Chem; 1971 Jan 01; 352(1):106-8. PubMed ID: 5540069
    [No Abstract] [Full Text] [Related]

  • 19. Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.
    Fontaine G, Résibois A, Tondeur M, Jonniaux G, Farriaux JP, Voet W, Maillard E, Loeb H.
    Acta Neuropathol; 1973 Jan 30; 23(2):118-32. PubMed ID: 4349527
    [No Abstract] [Full Text] [Related]

  • 20. [On a component of the mixture of brain gangliosides, which is transferred to the Tay-Sachs ganglioside under the influence of neuraminidase].
    Klenk E, Naoi M.
    Hoppe Seylers Z Physiol Chem; 1968 Mar 30; 349(3):288-92. PubMed ID: 4302220
    [No Abstract] [Full Text] [Related]

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