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Journal Abstract Search

113 related items for PubMed ID: 2743650

  • 1. Type III Machado-Joseph disease in a Japanese family: a clinicopathological study with special reference to the peripheral nervous system.
    Kanda T, Isozaki E, Kato S, Tanabe H, Oda M.
    Clin Neuropathol; 1989; 8(3):134-41. PubMed ID: 2743650
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  • 2. [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; 92(3):161-83. PubMed ID: 2353076
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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. [Machado-Joseph disease in a family of Spanish origin].
    Pou-Serradell A, Russi A, Ferrer I, Galofré E, Escudero D.
    Rev Neurol (Paris); 1987 Mar; 143(6-7):520-5. PubMed ID: 3477847
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  • 6. [An autopsied case of type 2 Machado-Joseph's disease or spino-pontine degeneration].
    Iwabuchi K, Nagatomo H, Tanabe T, Sakai H, Yagishita S.
    No To Shinkei; 1993 Aug; 45(8):733-40. PubMed ID: 8217397
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  • 7. Joseph's disease: clinical and pathological studies in a Japanese family.
    Yuasa T, Ohama E, Harayama H, Yamada M, Kawase Y, Wakabayashi M, Atsumi T, Miyatake T.
    Ann Neurol; 1986 Feb; 19(2):152-7. PubMed ID: 3963757
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  • 8. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Feb; 7(3):193-203. PubMed ID: 1620135
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  • 9. Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus.
    Subramony SH, Fratkin JD, Manyam BV, Currier RD.
    Mov Disord; 1996 Mar; 11(2):174-80. PubMed ID: 8684388
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  • 10. [A new family of Machado-Joseph disease--an abnormal decrease in signal intensity of the putamen in magnetic resonance imaging].
    Muramatsu S, Takiyama Y, Hanyu S, Niijima K, Yoshida M.
    Rinsho Shinkeigaku; 1990 Jul; 30(7):777-9. PubMed ID: 2242634
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  • 14. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
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  • 16. Was the ataxia of Pierre Marie Machado-Joseph disease?: A reappraisal based on the last autopsy case from la Salpêtrière Hospital.
    Uchihara T, Duyckaerts C, Iwabuchi K, Iwata M, Yagishita S, Hauw JJ.
    Arch Neurol; 2004 May; 61(5):784-90. PubMed ID: 15148161
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  • 18. The pathology of Machado-Joseph disease. Report of a possible homozygous case.
    Coutinho P, Guimarães A, Scaravilli F.
    Acta Neuropathol; 1982 May; 58(1):48-54. PubMed ID: 7136516
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  • 20. [An autopsied case of dentato-rubro-pallido-luysian atrophy with atypical pathological lesions].
    Konagaya M, Sakai M, Kato T, Kuru S, Matsuoka Y, Sobue G, Hashizume Y, Yoshida M.
    No To Shinkei; 2002 Jun; 54(6):513-20. PubMed ID: 12166103
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