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Journal Abstract Search

204 related items for PubMed ID: 4041292

  • 1. [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
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  • 3. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
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  • 4. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
    Kogure T, Oda T, Katoh Y.
    Seishin Shinkeigaku Zasshi; 1990 Mar; 92(3):161-83. PubMed ID: 2353076
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  • 7. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
    Iwabuchi K, Nakazawa Y, Akai J, Yagishita S, Amano N.
    No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439
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  • 11. [A case of atypical progressive supranuclear palsy with degeneration of the fronto-pontine tracts, and without grumose degeneration of the dentate nucleus].
    Inagaki T, Ishino H, Iijima M, Seno H, Kikumoto O, Yoshinaga J, Matsuura H, Tachiyama Y.
    No To Shinkei; 1996 Nov; 48(11):1037-45. PubMed ID: 8951896
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  • 12. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
    Berciano J, García A, Infante J.
    Handb Clin Neurol; 2013 Nov; 115():907-32. PubMed ID: 23931821
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  • 16. [An autopsy case of Marie's hereditary ataxia].
    Ishino H, Sato M, Mii T, Terano A, Hayahara T.
    Seishin Shinkeigaku Zasshi; 1971 Oct; 73(10):747-57. PubMed ID: 5168989
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  • 18. [An autopsy case of atypical Friedreich's ataxia with chronic idiopathic intestinal pseudo-obstruction].
    Nagata T, Aoki M, Hasegawa T, Shiga Y, Hayashi T, Higuchi J, Abe K, Tanno T, Konno H, Itoyama Y.
    Rinsho Shinkeigaku; 2001 Jul; 41(7):412-7. PubMed ID: 11808352
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  • 20. An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease).
    Kuru S, Sakai M, Konagaya M, Yoshida M, Hashizume Y, Saito K.
    Neuropathology; 2009 Feb; 29(1):63-7. PubMed ID: 18410269
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