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Journal Abstract Search

123 related items for PubMed ID: 5752596

  • 1. [Pathogenesis of Hallervorden-Spatz disease-its neuropathology from viewpoint of systemic degenerative disorder and precocious senility].
    Shiraki H.
    Shinkei Kenkyu No Shimpo; 1968 Aug; 12(2):389-413. PubMed ID: 5752596
    [No Abstract] [Full Text] [Related]

  • 2. [Aging and senility processes of the central nervous system from the neuropathological viewpoint].
    Shiraki H.
    Shinkei Kenkyu No Shimpo; 1967 Oct; 11(3):607-26. PubMed ID: 4873145
    [No Abstract] [Full Text] [Related]

  • 3. [Case of parkinsonism with degeneration of the outer globus pallidus--relationship to progressive atrophy of globus pallidus and Hallervorden-Spatz disease].
    Harada K, Koike M, Tomonaga M.
    Rinsho Shinkeigaku; 1972 Jul; 12(7):339-45. PubMed ID: 4674768
    [No Abstract] [Full Text] [Related]

  • 4. [Autopsy case of Hallervorden-Spatz disease: clinicopathological and biochemical study].
    Takashima S, Iwata Y, Tanaka K, Kurokawa T, Takeshita K.
    Shinkei Kenkyu No Shimpo; 1969 Jun; 13(2):249-59. PubMed ID: 5390671
    [No Abstract] [Full Text] [Related]

  • 5. [Autopsy case of Hallervorden-Spatz syndrome with Lewy body].
    Chichibu M, Oyake Y, Murone I.
    Shinkei Kenkyu No Shimpo; 1966 Dec; 10(4):700-7. PubMed ID: 6010161
    [No Abstract] [Full Text] [Related]

  • 6. [Late Hallervorden-Spatz disease with important reticular and cerebellar participation].
    Evrard E, Hariga J, Martin JJ, Reznik M.
    Psychiatr Neurol Neurochir; 1968 Dec; 71(3):243-54. PubMed ID: 5687405
    [No Abstract] [Full Text] [Related]

  • 7. [Early infantile familial forms of pigmentary pallido-reticular atrophy. Critical study of the value of histopathologic criteria in the differentiation of an infantile form of Hallervorden-Spatz disease].
    Fadiloglu S.
    Acta Neurol Belg; 1971 Dec; 71(5):392-406. PubMed ID: 5004231
    [No Abstract] [Full Text] [Related]

  • 8. [The Hallervorden-Spatz Disease].
    Seitelberger F.
    Nervenarzt; 1966 Nov; 37(11):482-93. PubMed ID: 5983175
    [No Abstract] [Full Text] [Related]

  • 9. Amyotrophic lateral sclerosis-dementia complex, neuroaxonal dystrophy, and Hallervorden-Spatz disease.
    Bots GT, Staal A.
    Neurology; 1973 Jan; 23(1):35-9. PubMed ID: 4734498
    [No Abstract] [Full Text] [Related]

  • 10. [Juvenile spongious degeneration of the central nervous system. Its relation to Hallervorden-Spatz disease and the neuro-axonal dystrophies].
    Brucher JM, Dom R, Robin A.
    Rev Neurol (Paris); 1968 Nov; 119(5):425-44. PubMed ID: 5715881
    [No Abstract] [Full Text] [Related]

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  • 12. Hallervorden spatz disease associated with lewy type inclusions.
    Bornstein B, Sandbank U, Fried Y.
    Confin Neurol; 1966 Nov; 27(5):397-405. PubMed ID: 5959225
    [No Abstract] [Full Text] [Related]

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  • 18. [Rapid evolution of presenile dementia in a case of Hallervorden-Spatz disease].
    Rizzuto N, Radermecker J.
    Acta Neurol (Napoli); 1967 Nov; 22(2):281-90. PubMed ID: 5304557
    [No Abstract] [Full Text] [Related]

  • 19. Hallervorden Spatz disease. Its pathogenesis and place among the axonal dystrophies.
    Sacks OW, Aguilar MJ, Borwn WJ.
    Acta Neuropathol; 1966 Mar 04; 6(2):164-74. PubMed ID: 5963287
    [No Abstract] [Full Text] [Related]

  • 20. Pathological assessment of movement disorders: requirements for documentation in brain banks.
    Jellinger KA, Lantos PL, Mehraein P.
    J Neural Transm Suppl; 1993 Mar 04; 39():173-84. PubMed ID: 8360658
    [Abstract] [Full Text] [Related]

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