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J-GLOBAL ID:201602272295155246   Reference number:16A1226728

Unusual Case of Cardiac Amyloidosis Preceded by a Twenty-year History of Dilated Cardiomyopathy and Heart Failure

20年間の拡張型心筋症および心不全歴が先行した心アミロイドーシスのまれな症例
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Volume: 55  Issue:Page: 1109-1115(J-STAGE)  Publication year: 2016 
JST Material Number: U0033A  ISSN: 1349-7235  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Cardiovascular system diseases 
Reference (23):
  • 1. Sipe JD, Benson MD, Buxbaum JN, et al. Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis. Amyloid 21: 221-224, 2014.
  • 2. Siqueira-Filho AG, Cunha CL, Tajik AJ, Seward JB, Schattenberg TT, Giuliani ER. M-mode and two-dimensional echocardiographic features in cardiac amyloidosis. Circulation 63: 188-196, 1981.
  • 3. Loizos S, Shiakalli Chrysa T, Christos GS. Amyloidosis: review and imaging findings. Semin Ultrasound CT MR 35: 225-239, 2014.
  • 4. Buja LM, Khoi NB, Roberts WC. Clinically significant cardiac amyloidosis. Clinicopathologic findings in 15 patients. Am J Cardiol 26: 394-405, 1970.
  • 5. Koike H, Misu K, Ikeda S, et al. Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form. Arch Neurol 59: 1771-1776, 2002.
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