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Journal Abstract Search

168 related items for PubMed ID: 1786932

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  • 4. [Transthyretin Arg-83 mutation in vitreous amyloidosis].
    Chen L, Lü L, Zhang P, Li Y, Lin J.
    Yan Ke Xue Bao; 2008 Mar; 24(1):65-7. PubMed ID: 18709962
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  • 11. 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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  • 12. Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.
    Saraiva MJ, Costa PP, Goodman DS.
    J Lab Clin Med; 1983 Oct; 102(4):590-603. PubMed ID: 6311926
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  • 13. Ocular changes in familial amyloidotic polyneuropathy with dense vitreous opacities.
    Monteiro JG, Martins AF, Figueira A, Saraiva MJ, Costa PP.
    Eye (Lond); 1991 Oct; 5 ( Pt 1)():99-105. PubMed ID: 2060679
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  • 14. Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis.
    Gustavsson A, Jahr H, Tobiassen R, Jacobson DR, Sletten K, Westermark P.
    Lab Invest; 1995 Nov; 73(5):703-8. PubMed ID: 7474944
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  • 17. 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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  • 18. Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities.
    Yazaki M, Connors LH, Eagle RC, Leff SR, Skinner M, Benson MD.
    Amyloid; 2002 Dec; 9(4):263-7. PubMed ID: 12557756
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  • 20. The molecular biology and clinical features of amyloid neuropathy.
    Benson MD, Kincaid JC.
    Muscle Nerve; 2007 Oct; 36(4):411-23. PubMed ID: 17554795
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