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Journal Abstract Search

123 related items for PubMed ID: 5172645

  • 1. Hereditary spastic ataxia: report of a family through four generations.
    Ishino H, Sato M, Terao A, Hayahara T, Otsuki S.
    Folia Psychiatr Neurol Jpn; 1971; 25(4):269-81. PubMed ID: 5172645
    [No Abstract] [Full Text] [Related]

  • 2. [Autopsy case of a family with hereditary ataxia].
    Fujimoto S, Tsuchimoto K, Inoue K, Nakamura K, Kanda M.
    No To Shinkei; 1976 Mar; 28(3):255-61. PubMed ID: 1036048
    [No Abstract] [Full Text] [Related]

  • 3. Marinesco-Sjögren syndrome. Report of an autopsy.
    Mahloudji M, Amirhakimi GH, Haghighi P, Khodadoust AA.
    Brain; 1972 Mar; 95(4):675-80. PubMed ID: 4647150
    [No Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Spino-pontine degeneration.
    Boller F, Segarra JM.
    Eur Neurol; 1969 Feb; 2(6):356-73. PubMed ID: 5808476
    [No Abstract] [Full Text] [Related]

  • 6. Menzel's hereditary ataxia with slow eye movements and myoclonus. A clinico-pathological study.
    Rondot P, De Recondo J, Davous P, Vedrenne C.
    J Neurol Sci; 1983 Sep; 61(1):65-80. PubMed ID: 6631453
    [Abstract] [Full Text] [Related]

  • 7. Chronic brainstem encephalitis with mental symptoms and ataxia: report of three cases with necropsy.
    Ueno T, Takahata N.
    J Neurol Neurosurg Psychiatry; 1978 Jun; 41(6):516-24. PubMed ID: 671063
    [Abstract] [Full Text] [Related]

  • 8. Opsoclonus, occult carcinoma, and chemical pathology in dentate nuclei.
    Ross AT, Zeman W.
    Arch Neurol; 1967 Nov; 17(5):546-51. PubMed ID: 6054608
    [No Abstract] [Full Text] [Related]

  • 9. [An autopsy case of hereditary ataxia (hereditary spastic ataxia)].
    Yagishita S, Nakano T, Iwabuchi K, Sakai H.
    No To Shinkei; 1985 Jun; 37(6):603-9. PubMed ID: 4041292
    [Abstract] [Full Text] [Related]

  • 10. Superficial hemosiderosis of the central nervous system.
    Kott E, Bechar M, Bornstein B, Askenasy HM, Sandbank U.
    Acta Neurochir (Wien); 1966 Jun; 14(3):287-98. PubMed ID: 5298356
    [No Abstract] [Full Text] [Related]

  • 11. Some clinical and pathological problems in neuro-Behçet's syndrome.
    Totsuka S, Midorikawa T.
    Folia Psychiatr Neurol Jpn; 1972 Jun; 26(4):275-84. PubMed ID: 4679092
    [No Abstract] [Full Text] [Related]

  • 12. [Dominantly inherited type of cerebellar ataxia].
    Becker PE, Sabuncu N, Hopf HC.
    Z Neurol; 1971 Apr 28; 199(1):116-39. PubMed ID: 4102742
    [No Abstract] [Full Text] [Related]

  • 13. [Autopsy case of Kufs' type of cerebral lipidosis].
    Ishizu H, Sarai K, Ishino H.
    Rinsho Shinkeigaku; 1972 Jan 28; 12(1):42-8. PubMed ID: 4674946
    [No Abstract] [Full Text] [Related]

  • 14. [Familial atrophic form of spinocerebellar ataxia].
    Gaj T, Grendus-Tota B.
    Neurol Neurochir Pol; 1973 Jan 28; 7(5):679-83. PubMed ID: 4763007
    [No Abstract] [Full Text] [Related]

  • 15. Distribution of plaques in seventy autopsy cases of multiple sclerosis in the United States.
    Ikuta F, Zimmerman HM.
    Neurology; 1976 Jun 28; 26(6 PT 2):26-8. PubMed ID: 944889
    [No Abstract] [Full Text] [Related]

  • 16. Dominant spino-pontine atrophy. Report of a family through three generations.
    Taniguchi R, Konigsmark BW.
    Brain; 1971 Jun 28; 94(2):349-58. PubMed ID: 5571046
    [No Abstract] [Full Text] [Related]

  • 17. Uncommon syndromes of cerebellar vermis aplasia. I: Joubert syndrome.
    Friede RL, Boltshauser E.
    Dev Med Child Neurol; 1978 Dec 28; 20(6):758-63. PubMed ID: 729929
    [Abstract] [Full Text] [Related]

  • 18. Neuropathology of subacute myelo-optico-neuropathy, "SMON".
    Shiraki H.
    Jpn J Med Sci Biol; 1971 Aug 28; 24(4):217-43. PubMed ID: 5316312
    [No Abstract] [Full Text] [Related]

  • 19. 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 28; 51(3):383-94. PubMed ID: 7276985
    [Abstract] [Full Text] [Related]

  • 20. [Neuropathological studies on neuro-Behçet's syndrome].
    Totsuka S, Yazaki M, Asayama R, Nagao K.
    Shinkei Kenkyu No Shimpo; 1972 Jun 28; 16(3):471-6. PubMed ID: 5066189
    [No Abstract] [Full Text] [Related]

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