Light‐chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome-Reference-Cited by-同舟云学术

Light‐chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome

Published:2020-02-20 Issue:10 Volume:22 Page:1852-1862
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:Eur J Heart Fail

Author:

Nitsche Christian¹,Aschauer Stefan¹,Kammerlander Andreas A.¹,Schneider Matthias¹,Poschner Thomas¹,Duca Franz¹,Binder Christina¹,Koschutnik Matthias¹,Stiftinger Julian¹,Goliasch Georg¹,Siller‐Matula Jolanta¹,Winter Max‐Paul¹,Anvari‐Pirsch Anahit¹,Andreas Martin²,Geppert Alexander³,Beitzke Dietrich⁴,Loewe Christian⁴,Hacker Marcus⁵,Agis Hermine⁶,Kain Renate⁷,Lang Irene¹,Bonderman Diana¹,Hengstenberg Christian¹,Mascherbauer Julia¹

Affiliation:

1. Division of Cardiology, Department of Internal Medicine II Medical University of Vienna Vienna Austria

2. Department of Cardiac Surgery Medical University of Vienna Vienna Austria

3. Department of Internal Medicine III, Division of Cardiology Wilhelminenspital Vienna Austria

4. Department of Cardiovascular and Interventional Radiology, Department of Radiology Medical University of Vienna Vienna Austria

5. Department of Nuclear Medicine Medical University of Vienna Vienna Austria

6. Division of Oncology, Department of Internal Medicine I Medical University of Vienna Vienna Austria

7. Department of Pathology Medical University of Vienna Vienna Austria

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejhf.1756

Reference35 articles.

1. Prevalence of aortic valve abnormalities in the elderly: An echocardiographic study of a random population sample

2. The Global Burden of Aortic Stenosis

3. Pathophysiology and treatment of cardiac amyloidosis

4. Assessment of Myocardial Fibrosis With Cardiovascular Magnetic Resonance

5. AL (Light-Chain) Cardiac Amyloidosis

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