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Familial amyloidosis

1992; Wiley; Volume: 232; Issue: 6 Linguagem: Finlandês

10.1111/j.1365-2796.1992.tb00632.x

1365-2796

M D Benson, Robert A. Kyle,

Amyloidosis: Diagnosis, Treatment, Outcomes

Journal of Internal MedicineVolume 232, Issue 6 p. 525-527 Familial amyloidosis M. D. BENSON, M. D. BENSON Rheumatology Division, V.A. Medical Center, Indianapolis, IN, USASearch for more papers by this authorRobert A. Kyle MD, Corresponding Author Robert A. Kyle MDMayo Clinic, 200 First Street SW, Rochester, Minnesota 55905, USASearch for more papers by this author M. D. BENSON, M. D. BENSON Rheumatology Division, V.A. Medical Center, Indianapolis, IN, USASearch for more papers by this authorRobert A. Kyle MD, Corresponding Author Robert A. Kyle MDMayo Clinic, 200 First Street SW, Rochester, Minnesota 55905, USASearch for more papers by this author First published: December 1992 https://doi.org/10.1111/j.1365-2796.1992.tb00632.xCitations: 6AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Benson MD, Wallace MR. Amyloidosis. In: CR Scriver, AL Beaudet, WS Sly, D. Valle, eds. The Metabolic Basis of Inherited Disease, 6th ed. Vol 2. New York: McGraw-Hill, 1989: 2439–60. Google Scholar 2 Wallace MR, Naylor SL, Kluve-Beckerman B. et al. Localization of the human prealbumin gene to chromosome 18. Biochem Biophys Res Commun 1985; 129: 753–8. 10.1016/0006-291X(85)91956-4 CASPubMedWeb of Science®Google Scholar 3 Moses AC, Rosen HN, Moller DE et al. A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia. J Clin Invest 1990; 86: 2025–33. 10.1172/JCI114938 CASPubMedWeb of Science®Google Scholar 4 Nichols WC, Gregg RE, Brewer HB Jr, Benson MD. A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. Genomics 1990; 8: 318–23. 10.1016/0888-7543(90)90288-6 CASPubMedWeb of Science®Google Scholar Citing Literature Volume232, Issue6December 1992Pages 525-527 ReferencesRelatedInformation