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Journal Abstract Search

162 related items for PubMed ID: 2847318

  • 1.
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  • 2. Genetic factors in amyloidosis.
    Thomas PK.
    J Med Genet; 1975 Dec; 12(4):317-26. PubMed ID: 176361
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  • 3. Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies.
    Gafni J, Fischel B, Reif R, Yaron M, Pras M.
    Q J Med; 1985 Apr; 55(216):33-44. PubMed ID: 3859886
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  • 6. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients.
    Ikeda S, Hanyu N, Hongo M, Yoshioka J, Oguchi H, Yanagisawa N, Kobayashi T, Tsukagoshi H, Ito N, Yokota T.
    Brain; 1987 Apr; 110 ( Pt 2)():315-37. PubMed ID: 3032328
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  • 10. Familial amyloid polyneuropathy: report of an autopsy case with neuropathy, vitreous opacities and polycystic kidney.
    Scelsi R, Verri AP, Bono G, Marbini A.
    Eur Neurol; 1989 Apr; 29(1):27-32. PubMed ID: 2540006
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  • 11. Familial amyloid polyneuropathy. Demonstration of prealbumin in a kinship of German/English ancestry with onset in the seventh decade.
    Libbey CA, Rubinow A, Shirahama T, Deal C, Cohen AS.
    Am J Med; 1984 Jan; 76(1):18-24. PubMed ID: 6691355
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  • 12. Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindred.
    Ueno S, Fujimura H, Yorifuji S, Nakamura Y, Takahashi M, Tarui S, Yanagihara T.
    Brain; 1992 Oct; 115 ( Pt 5)():1275-89. PubMed ID: 1330202
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  • 13. Heart valve involvement in familial amyloidosis with polyneuropathy.
    Eriksson A, Olofsson BO, Eriksson P.
    Pathol Res Pract; 1986 Oct; 181(5):563-7. PubMed ID: 3786249
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  • 14. Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M).
    Lobato L.
    J Nephrol; 2003 Oct; 16(3):438-42. PubMed ID: 12832749
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  • 16. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis.
    Holmgren G, Ericzon BG, Groth CG, Steen L, Suhr O, Andersen O, Wallin BG, Seymour A, Richardson S, Hawkins PN.
    Lancet; 1993 May 01; 341(8853):1113-6. PubMed ID: 8097803
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  • 17. Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy.
    Lobato L, Beirão I, Silva M, Bravo F, Silvestre F, Guimarães S, Sousa A, Noël LH, Sequeiros J.
    Nephrol Dial Transplant; 2003 Mar 01; 18(3):532-8. PubMed ID: 12584275
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  • 19. Type I familial amyloidotic polyneuropathy (Japanese type).
    Araki S.
    Brain Dev; 1984 Mar 01; 6(2):128-33. PubMed ID: 6087691
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