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Journal Abstract Search

144 related items for PubMed ID: 7136516

  • 1. The pathology of Machado-Joseph disease. Report of a possible homozygous case.
    Coutinho P, Guimarães A, Scaravilli F.
    Acta Neuropathol; 1982; 58(1):48-54. PubMed ID: 7136516
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  • 2. 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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  • 3. Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorena Portuguese family.
    Lima L, Coutinho P.
    Neurology; 1980 Mar; 30(3):319-22. PubMed ID: 7189034
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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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  • 5. [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. 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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  • 7. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A, Stefanko SZ, Jennekens FG, Vries-Bos LH, van Gijn J.
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):648-52. PubMed ID: 6886703
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  • 8. [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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  • 10. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE.
    Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668
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  • 13. 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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  • 14. Machado-Joseph disease: the vestibular presentation.
    Mallinson AI, Longridge NS, McLeod PM.
    J Otolaryngol; 1986 Jun; 15(3):184-8. PubMed ID: 3487657
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  • 15. Retinopathy associated with Machado--Joseph disease (spinocerebellar ataxia 3) with CAG trinucleotide repeat expansion.
    Isashiki Y, Kii Y, Ohba N, Nakagawa M.
    Am J Ophthalmol; 2001 Jun; 131(6):808-10. PubMed ID: 11384587
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  • 16. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Jun; 7(3):193-203. PubMed ID: 1620135
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  • 17. Sporadic case resembling autosomal-dominant motor system degeneration (Azorean disease complex).
    McQuinn BA, Kemper TL.
    Arch Neurol; 1987 Mar; 44(3):341-4. PubMed ID: 3827687
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  • 18. The natural history of Machado-Joseph disease. An analysis of 138 personally examined cases.
    Barbeau A, Roy M, Cunha L, de Vincente AN, Rosenberg RN, Nyhan WL, MacLeod PL, Chazot G, Langston LB, Dawson DM.
    Can J Neurol Sci; 1984 Nov; 11(4 Suppl):510-25. PubMed ID: 6509398
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  • 20. Machado-Joseph-Azorean disease in India.
    Bharucha NE, Bharucha EP, Bhabha SK.
    Arch Neurol; 1986 Feb; 43(2):142-4. PubMed ID: 3947253
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