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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 4283420

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  • 4. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y, Kito S, Itoga E, Kajiwara H.
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
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  • 6. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
    Hayashi Y, Tomita M, Shimizu K, Takamiya M, Watanabe H.
    Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963
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  • 7. [Triplet repeat expansions in hereditary neurodegenerative diseases].
    Peñuelas I, de Miguel C, Gullón A.
    Med Clin (Barc); 1997 Apr 12; 108(14):542-8. PubMed ID: 9190441
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  • 8. [A family of familial amyloidosis with cerebellar ataxia and pyramidal tract sign--clinical and genetic study (author's transl)].
    Kobayashi T, Nakagawa S, Oguchi K, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1978 Sep 12; 18(9):515-24. PubMed ID: 709971
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  • 10. [Cardiomyopathy in Heredofamilial Neuromyopathies (author's transl)].
    Sekiguchi M, Numao Y, Hiroe M.
    Kokyu To Junkan; 1975 Mar 12; 23(3):209-24. PubMed ID: 1093249
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  • 11. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)].
    Fujimori N, Hanyu N, Oguchi K, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1980 Jun 12; 20(6):423-9. PubMed ID: 7408341
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  • 13. [Marie's ataxia with nuclear external ophthalmoplegia and muscle atrophy of lower extremities--report of an autopsy case and its family (author's transl)].
    Kurachi M, Shibata T, Koyama Y, Isaki K, Yamaguchi N.
    Seishin Shinkeigaku Zasshi; 1977 Jun 12; 79(1):1-25. PubMed ID: 577311
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  • 16. [Clinico-genalogic characteristics of hereditary diseases of the nervous system in the Kuibyshev region].
    Nesterov LN, Sushcheva GP, Viatkina SIa.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978 Jun 12; 78(10):1506-12. PubMed ID: 152555
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  • 17. [Neurodegenerative disorders and the role of trinucleotide repeat expansion. I. The diseases].
    Kremer HP, Knoers NV.
    Ned Tijdschr Geneeskd; 1996 Nov 23; 140(47):2325-9. PubMed ID: 8984394
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  • 18. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
    Ben Hamida M, Madani S, Zmerli S, Chami I, Annabi A, Jamoussi M, Marzouki M, Rachdi M, Samoud S, Talbi M.
    Rev Neurol (Paris); 1980 Nov 23; 136(8-9):495-508. PubMed ID: 7221327
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  • 19. Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Adv Neurol; 1984 Nov 23; 41():179-93. PubMed ID: 6388271
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