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Journal Abstract Search

141 related items for PubMed ID: 7189034

  • 1. 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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  • 2. The pathology of Machado-Joseph disease. Report of a possible homozygous case.
    Coutinho P, Guimarães A, Scaravilli F.
    Acta Neuropathol; 1982 Mar; 58(1):48-54. PubMed ID: 7136516
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  • 3. 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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  • 5. Autosomal dominant motor system degeneration in a black family.
    Cooper JA, Nakada T, Knight RT, Friedland RP.
    Ann Neurol; 1983 Nov; 14(5):585-7. PubMed ID: 6651242
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  • 8. Presumably Azorean disease in a presumably non-Portuguese family.
    Healton EB, Brust JC, Kerr DL, Resor S, Penn A.
    Neurology; 1980 Oct; 30(10):1084-9. PubMed ID: 7191499
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  • 11. A small 55-repeat MJD1 CAG allele in a patient with Machado-Joseph disease and abnormal eye movements.
    Egan RA, Camicioli R, Popovich BW.
    Eur Neurol; 2000 Oct; 44(3):189-90. PubMed ID: 11053973
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  • 12. [Machado-Joseph disease: description of 5 members of a family].
    Teive HA, Arruda WO, Trevisol-Bittencourt PC.
    Arq Neuropsiquiatr; 1991 Jun; 49(2):172-9. PubMed ID: 1810235
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  • 13. Machado-Joseph-Azorean disease. A ten-year study.
    Fowler HL.
    Arch Neurol; 1984 Sep; 41(9):921-5. PubMed ID: 6477227
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  • 14. Machado-Joseph disease in a Sicilian-American family.
    Suite ND, Sequeiros J, McKhann GM.
    J Neurogenet; 1986 May; 3(3):177-82. PubMed ID: 3734949
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  • 15. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 May; 7(3):193-203. PubMed ID: 1620135
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  • 16. [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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  • 17. A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q.
    Takiyama Y, Oyanagi S, Kawashima S, Sakamoto H, Saito K, Yoshida M, Tsuji S, Mizuno Y, Nishizawa M.
    Neurology; 1994 Jul; 44(7):1302-8. PubMed ID: 8035935
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  • 19. [Machado-Joseph disease in a family of Spanish origin].
    Pou-Serradell A, Russi A, Ferrer I, Galofré E, Escudero D.
    Rev Neurol (Paris); 1987 Jul; 143(6-7):520-5. PubMed ID: 3477847
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  • 20. Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.
    Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S.
    J Neurol Sci; 1996 Oct; 142(1-2):140-7. PubMed ID: 8902734
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