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January 6, 2014Expert Review of Cardiovascular Therapy20 citations

Cardiac amyloidosis

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SYSyed Wamique YusufASAmirreza SolhpourJBJosé Banchs

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Abstract

Amyloidosis is a condition characterized by the extracellular deposition of insoluble fibrillar protein in tissues and various organs including the heart. This review summarizes the clinical manifestations and diagnostic treatment approaches for cardiac amyloidosis.

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Yusuf et al. (2014) studied this question.

synapsesocial.com/papers/6a1229708edbaba0bf66c14chttps://doi.org/10.1586/14779072.2014.876363
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Use of Abdominal Fat Tissue Aspirate in the Diagnosis of Systemic Amyloidosis1983 · 202 citations
  2. 2Unique type of isolated cardiac valvular amyloidosis2006 · 13 citations
  3. 3A Trial of Three Regimens for Primary Amyloidosis: Colchicine Alone, Melphalan and Prednisone, and Melphalan, Prednisone, and Colchicine1997 · 693 citations
  4. 4Intracardiac Thrombosis and Anticoagulation Therapy in Cardiac Amyloidosis2009 · 286 citations
  5. 5Treatment options for severe cardiac amyloidosis: heart transplantation combined with chemotherapy and stem cell transplantation for patients with AL-amyloidosis and heart and liver transplantation for patients with ATTR-amyloidosis☆2007 · 67 citations