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Journal Abstract Search

248 related items for PubMed ID: 3479441

  • 1. 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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  • 2. Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy.
    Sakaki Y, Yoshioka K, Tanahashi H, Furuya H, Sasaki H.
    Mol Biol Med; 1989 Apr; 6(2):161-8. PubMed ID: 2693890
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  • 3. Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan.
    Harada T, Kito S, Ishizaki F, Matsubayashi H, Katayama S, Sasaki H, Furuya H, Sakaki Y.
    Res Commun Chem Pathol Pharmacol; 1989 Aug; 65(2):237-44. PubMed ID: 2587841
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  • 6. Familial amyloidotic polyneuropathy: report of patients heterozygous for the transthyretin Gly42 gene.
    Murakami T, Yi S, Yamamoto K, Maruyama S, Araki S.
    Ann Neurol; 1992 Mar; 31(3):340-2. PubMed ID: 1637142
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  • 12. [Diagnosis by recombinant DNA techniques and clinical features of familial amyloid polyneuropathy].
    Harada T.
    No To Shinkei; 1988 Jul; 40(7):617-21. PubMed ID: 2852018
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  • 16. 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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  • 17. [DNA tests for mutant genes coding for transthyretins Gly42, Arg50 and Cys114 in Japanese cases of familial amyloid polyneuropathy].
    Uemichi T, Ueno S, Takahashi N, Soga F, Yorifuji S, Tarui S.
    Rinsho Shinkeigaku; 1991 Oct; 31(10):1151-4. PubMed ID: 1686993
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