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Journal Abstract Search

260 related items for PubMed ID: 1637142

  • 1. 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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  • 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. Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
    Koeppen AH, Wallace MR, Benson MD, Altland K.
    Muscle Nerve; 1990 Nov; 13(11):1065-75. PubMed ID: 2122246
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  • 4. [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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  • 5. Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy.
    Yoshioka K, Sasaki H, Yoshioka N, Furuya H, Harada T, Kito S, Sakaki Y.
    Mol Biol Med; 1986 Aug; 3(4):319-28. PubMed ID: 3022107
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  • 7. 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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  • 8. 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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  • 10. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy.
    Nakazato M, Sasaki H, Furuya H, Sakaki Y, Kurihara T, Matsukura S, Kangawa K, Matsuo H.
    Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992
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  • 11. Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy.
    Maeda S, Mita S, Araki S, Shimada K.
    Mol Biol Med; 1986 Aug; 3(4):329-38. PubMed ID: 3022108
    [Abstract] [Full Text] [Related]

  • 12. Prealbumin variants in the amyloid fibrils of Swedish familial amyloidotic polyneuropathy.
    Westermark P, Sletten K, Olofsson BO.
    Clin Exp Immunol; 1987 Sep; 69(3):695-701. PubMed ID: 3117463
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  • 14. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
    Augustin S, Llige D, Andreu A, González A, Genescà J.
    Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
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  • 15. Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy.
    Jones LA, Skare JC, Harding JA, Cohen AS, Milunsky A, Skinner M.
    Am J Hum Genet; 1991 May; 48(5):979-82. PubMed ID: 1850191
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  • 17. Cloning of human prealbumin complementary DNA. Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy.
    Whitehead AS, Skinner M, Bruns GA, Costello W, Edge MD, Cohen AS, Sipe JD.
    Mol Biol Med; 1984 Dec; 2(6):411-23. PubMed ID: 6100724
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  • 18. [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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  • 19. Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. Online.
    Booth DR, Gillmore JD, Persey MR, Booth SE, Cafferty KD, Tennent GA, Madhoo S, Cochrane SW, Whitehead TC, Pasvol G, Hawkins PN.
    Hum Mutat; 1998 Sep; 12(2):135. PubMed ID: 10694917
    [Abstract] [Full Text] [Related]

  • 20. [A sporadic case of late onset familial amyloidotic polyneuropathy preceded by cardiac involvement].
    Aoki K, Koike R, Yuasa T, Ikeda S, Tsuji S.
    Rinsho Shinkeigaku; 1993 Aug; 33(8):905-8. PubMed ID: 8261706
    [Abstract] [Full Text] [Related]

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