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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 6093483

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Adv Neurol; 1984; 41():179-93. PubMed ID: 6388271
    [No Abstract] [Full Text] [Related]

  • 3. The neuropathology of olivopontocerebellar atrophy.
    Koeppen AH, Barron KD.
    Adv Neurol; 1984; 41():13-38. PubMed ID: 6388270
    [No Abstract] [Full Text] [Related]

  • 4.
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  • 5. Disorders of ocular motility in the olivopontocerebellar atrophies.
    Lepore FE.
    Adv Neurol; 1984; 41():97-103. PubMed ID: 6388272
    [No Abstract] [Full Text] [Related]

  • 6. Four biochemically different types of dominantly inherited olivopontocerebellar atrophy.
    Perry TL.
    Adv Neurol; 1984; 41():205-16. PubMed ID: 6149676
    [No Abstract] [Full Text] [Related]

  • 7.
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  • 8. Dominant olivopontocerebellar degeneration and optic pathway atrophy: a family report.
    Triau E, Dom R, Ververken D, Carton H.
    Clin Neuropathol; 1982; 1(2):67-72. PubMed ID: 7168919
    [No Abstract] [Full Text] [Related]

  • 9.
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  • 10. Cerebellodiencephalic interactions in olivopontocerebellar atrophy.
    Narabayashi H.
    Adv Neurol; 1984; 41():87-95. PubMed ID: 6496231
    [No Abstract] [Full Text] [Related]

  • 11.
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  • 12. Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis.
    Huang YP, Plaitakis A.
    Adv Neurol; 1984; 41():39-85. PubMed ID: 6496229
    [No Abstract] [Full Text] [Related]

  • 13. Autonomic dysfunction in olivopontocerebellar atrophy.
    Chokroverty S.
    Adv Neurol; 1984; 41():105-41. PubMed ID: 6388269
    [No Abstract] [Full Text] [Related]

  • 14. [Neuroradiologic and neurophysiologic studies in patients with olivo-ponto-cerebellar atrophy].
    Rossi L, Zappoli F, De Scisciolo G, Bindi A, Costantini S, Amantini A, Ronchi O, Pagnini P, Marini P, Zappoli R.
    Riv Neurobiol; 1984; 30(2-3):575-89. PubMed ID: 6544507
    [No Abstract] [Full Text] [Related]

  • 15. Heredo - familial spinocerebellar degeneration with slow eye movements--another variety of olivopontocerebellar degeneration.
    Wadia NH.
    Neurol India; 1977 Sep; 25(3):147-60. PubMed ID: 613260
    [No Abstract] [Full Text] [Related]

  • 16. Olivopontocerebellar atrophy in children: a report of seven cases in two families.
    Colan RV, Snead OC, Ceballos R.
    Ann Neurol; 1981 Oct; 10(4):355-63. PubMed ID: 7316488
    [Abstract] [Full Text] [Related]

  • 17.
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  • 18. [The hereditary cerebello-olivary atrophy (Holmes type) (author's transl)].
    Neundörfer B, Dietrich B, Scharf R.
    Nervenarzt; 1979 Oct; 50(10):626-30. PubMed ID: 537654
    [No Abstract] [Full Text] [Related]

  • 19.
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  • 20. [Epidemiology and clinical polymorphism of hereditary ataxia].
    Shutov AA, Dedik GK.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978 Oct; 78(6):825-30. PubMed ID: 676607
    [Abstract] [Full Text] [Related]

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