Cardiac amyloidosis: pathogenesis, clinical context, diagnosis and management options-Reference-Cited by-同舟云学术

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Cardiac amyloidosis: pathogenesis, clinical context, diagnosis and management options

Published:2017-07-04 Issue:4 Volume:72 Page:380-389
ISSN:0001-5385
Container-title:Acta Cardiologica
language:en
Short-container-title:Acta Cardiologica

Author:

Alkhawam Hassan¹,Patel Darshan²,Nguyen James²,Easaw Saumya Mariam²,Al-Sadawi Mohammed³,Syed Umer²,Zaiem Feras⁴,Homsi Maher²,Vittorio Timothy J.³

Affiliation:

1. Department of Medicine (Cardiology), Saint Louis University School of Medicine. St Louis, MO, USA;

2. Department of Medicine, Icahn School of Medicine at Mount Sinai, Elmhurst, NY, USA;

3. Center for Advanced Cardiac Therapeutics, St. Francis Hospital – The Heart Center®, Roslyn, NY, USA;

4. Mayo Evidence Based Practice Center – Mayo Clinic, Rochester, MN, USA

Publisher

Informa UK Limited

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/00015385.2017.1335034

Reference49 articles.

1. Amyloid fibrils

2. Immunoglobulin light chain variable (V) region genes influence clinical presentation and outcome in light chain–associated amyloidosis (AL)

3. Transthyretin (TTR) Cardiac Amyloidosis

4. Senile Systemic Amyloidosis Presenting With Heart Failure

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