These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 4374511

  • 1. GM1 gangliosidosis.
    Taori GM, Basu DK, Chandi S, Raman PT, Abraham J, Leelavathy R, Job CK.
    J Neurol Sci; 1974 Jan; 21(1):77-92. PubMed ID: 4374511
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. A type of juvenile cerebromacular degeneration characterized by granular osmiophilic deposits.
    Carpenter S, Karpati G, Wolfe LS, Andermann F.
    J Neurol Sci; 1973 Jan 30; 18(1):67-87. PubMed ID: 4120484
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Abnormal accumulation of sialoglycoproteins in a case of late infantile amaurotic idiocy.
    Adelman LS, Young E, Bass NH.
    Neurology; 1974 Nov 30; 24(11):1045-50. PubMed ID: 4371546
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Case of late infantile form of gangliosidosis G-M1].
    Majdecki T, Ryniewicz B.
    Neurol Neurochir Pol; 1975 Nov 30; 9(2):271-3. PubMed ID: 168506
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Subcellular fractions from Tay-Sachs brains: ganglioside, lipid, and protein composition and hexosaminidase activities.
    Kornguth S, Wannamaker B, Kolodny E, Geison R, Scott G, O'Brien JF.
    J Neurol Sci; 1974 Jul 30; 22(3):383-406. PubMed ID: 4857837
    [No Abstract] [Full Text] [Related]

  • 16. Gm-gangliosidosis type I: in utero detection and fetal manifestations.
    Kaback MM, Sloan HR, Sonneborn M, Herndon RM, Percy AK.
    J Pediatr; 1973 Jun 30; 82(6):1037-41. PubMed ID: 4702895
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. The white matter in G M2 gangliosidosis. A comparative histopathological and biochemical study.
    Haberland C, Brunngraber E, Witting L, Brown B.
    Acta Neuropathol; 1973 Mar 30; 24(1):43-55. PubMed ID: 4267001
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. The liver in GM1 gangliosidosis types 1 and 2. A light and electron microscopical study.
    Petrelli M, Blair JD.
    Arch Pathol; 1975 Feb 30; 99(2):111-6. PubMed ID: 1115681
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.