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Journal Abstract Search

201 related items for PubMed ID: 3379433

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  • 5. Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.
    Furuya H, Yoshioka K, Sasaki H, Sakaki Y, Nakazato M, Matsuo H, Nakadai A, Ikeda S, Yanagisawa N.
    J Clin Invest; 1987 Dec; 80(6):1706-11. PubMed ID: 3479441
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  • 6. Familial amyloidotic polyneuropathy (ATTR Ser50Ile): the first autopsy case report.
    Sakashita N, Ando Y, Obayashi K, Terazaki H, Yamashita T, Takei M, Kinjo M, Takahashi K.
    Virchows Arch; 2000 Apr; 436(4):345-50. PubMed ID: 10834537
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  • 7. [Familial amyloidotic polyneuropathy without familial occurrence but with asymptomatic carriers discovered by radioimmunoassay of variant transthyretin].
    Matsubara E, Tanaka M, Hirai S, Okamoto K, Nakazato M.
    Rinsho Shinkeigaku; 1988 Mar; 28(3):275-9. PubMed ID: 2841056
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  • 8. Familial amyloidotic polyneuropathy with late-onset and well-preserved autonomic function: a Japanese kindred with novel mutant transthyretin (Ala97 to Gly).
    Yasuda T, Sobue G, Doyu M, Nakazato M, Shiomi K, Yanagi T, Mitsuma T.
    J Neurol Sci; 1994 Jan; 121(1):97-102. PubMed ID: 8133316
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  • 9. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
    Saraiva MJ, Sherman W, Goodman DS.
    J Lab Clin Med; 1986 Jul; 108(1):17-22. PubMed ID: 3011930
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  • 10. [A late onset familial amyloidotic polyneuropathy (FAP) with a novel variant transthyretin characterized by a basic-for-acidic amino acid substitution (Glu61-->Lys)].
    Yamamoto T, Matsunaga K, Ohnishi A, Nakazato M, Murai Y.
    Rinsho Shinkeigaku; 1996 Sep; 36(9):1065-8. PubMed ID: 8976129
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  • 11. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset.
    Nakazato M, Kurihara T, Matsukura S, Kangawa K, Matsuo H.
    J Clin Invest; 1986 May; 77(5):1699-703. PubMed ID: 3457802
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  • 15. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
    Saraiva MJ, Birken S, Costa PP, Goodman DS.
    J Clin Invest; 1984 Jul; 74(1):104-19. PubMed ID: 6736244
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  • 17. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy.
    Saraiva MJ, Costa PP, Goodman DS.
    Neurology; 1986 Nov; 36(11):1413-7. PubMed ID: 3762958
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  • 20. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
    Holmgren G, Haettner E, Nordenson I, Sandgren O, Steen L, Lundgren E.
    Clin Genet; 1988 Nov; 34(5):333-8. PubMed ID: 3229002
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