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PUBMED FOR HANDHELDS

Journal Abstract Search


260 related items for PubMed ID: 6388270

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

  • 2. A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy.
    Wadia NH.
    Adv Neurol; 1984; 41():149-77. PubMed ID: 6093483
    [No Abstract] [Full Text] [Related]

  • 3. Dominant olivopontocerebellar atrophy with dementia and extrapyramidal signs: report of a family through three generations.
    Konigsmark BW, Lipton HL.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):178-91. PubMed ID: 5173358
    [Abstract] [Full Text] [Related]

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

  • 7. Autonomic nerve calcification and peripheral neuropathy in olivopontocerebellar atrophy.
    Staal A, Stefanko SZ, Busch HF, Jennekens FG, De Bruinj WC.
    J Neurol Sci; 1981 Sep; 51(3):383-94. PubMed ID: 7276985
    [Abstract] [Full Text] [Related]

  • 8. 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
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  • 11. Adrenoleukodystrophy with olivopontocerebellar atrophy-like lesions.
    Tateishi J, Sato Y, Suetsugu M, Takashiba T.
    Clin Neuropathol; 1986 Oct; 5(1):34-9. PubMed ID: 3948452
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  • 12. The pharmacology of olivopontocerebellar atrophy.
    Goetz CG, Tanner CM, Klawans HL.
    Adv Neurol; 1984 Oct; 41():143-8. PubMed ID: 6496225
    [No Abstract] [Full Text] [Related]

  • 13. Sporadic multi-system atrophy with early onset and rapid fatal outcome (atypical O.P.C.A.?). Case report.
    Barontini F, Marconi GP, Arnetoli G.
    Riv Patol Nerv Ment; 1983 Oct; 104(6):243-54. PubMed ID: 6543985
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  • 14. Spino-pontine degeneration.
    Boller F, Segarra JM.
    Eur Neurol; 1969 Oct; 2(6):356-73. PubMed ID: 5808476
    [No Abstract] [Full Text] [Related]

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

  • 16. Histochemical mapping on the distribution of simple esterase and acetylcholinesterase in the medulla oblongata, cerebellum and spinal cord of mouse.
    Sood PP, Bohra MH.
    J Hirnforsch; 1977 Oct; 18(1):75-87. PubMed ID: 894017
    [No Abstract] [Full Text] [Related]

  • 17. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S, De Recondo J.
    Rev Neurol (Paris); 1967 May; 116(5):383-400. PubMed ID: 6052813
    [No Abstract] [Full Text] [Related]

  • 18. Glutamate and pyruvate dehydrogenase deficiency in spinocerebellar degeneration.
    Maruyama S, Yamaguchi T.
    Adv Neurol; 1984 May; 41():255-65. PubMed ID: 6437168
    [No Abstract] [Full Text] [Related]

  • 19. The hereditary ataxias.
    Skre H, Haugstad TS, Berg K.
    Prog Med Genet; 1985 May; 6():123-240. PubMed ID: 2425393
    [No Abstract] [Full Text] [Related]

  • 20. Ultrastructural studies of olivopontocerebellar atrophy.
    Petito CK, Hart MN, Porro RS, Earle KM.
    J Neuropathol Exp Neurol; 1973 Oct; 32(4):503-22. PubMed ID: 4357157
    [No Abstract] [Full Text] [Related]


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