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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

192 related items for PubMed ID: 8133316

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  • 2. Familial amyloid polyneuropathy related to transthyretin Gly42 in a Japanese family.
    Uemichi T, Ueno S, Fujimura H, Umekage T, Yorifuji S, Matsuzawa Y, Tarui S.
    Muscle Nerve; 1992 Aug; 15(8):904-11. PubMed ID: 1353861
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  • 3. Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy.
    Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A.
    Neurology; 1992 Oct; 42(10):2045-7. PubMed ID: 1407590
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  • 5. 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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  • 6. Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70.
    Izumoto S, Younger D, Hays AP, Martone RL, Smith RT, Herbert J.
    Neurology; 1992 Nov; 42(11):2094-102. PubMed ID: 1436517
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  • 14. [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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  • 16. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
    Tanaka M, Hirai S, Matsubara E, Okamoto K, Morimatsu M, Nakazato M.
    J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433
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