Transthyretin cardiac amyloidosis in patients after TAVR: clinical and echocardiographic findings and long term survival-Reference-Cited by-同舟云学术

Transthyretin cardiac amyloidosis in patients after TAVR: clinical and echocardiographic findings and long term survival

Published:2021-10-26 Issue:6 Volume:8 Page:4549-4561
ISSN:2055-5822
Container-title:ESC Heart Failure
language:en
Short-container-title:ESC Heart Failure

Author:

Shimoni Sara¹²^ORCID,Zikri Meital¹,Haberman Dan¹,Livschitz Shay¹,Tshori Sagi¹²,Fabricant Yacov¹,Meledin Valery¹,Gandelman Gera¹,Goland Sorel¹²,George Jacob¹²

Affiliation:

1. The Heart Center, Kaplan Medical Center Rehovot Israel

2. Hadassah Medical School Hebrew University Jerusalem Israel

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ehf2.13667

Reference37 articles.

1. Transthyretin (TTR) Cardiac Amyloidosis

2. Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis

3. Nonbiopsy Diagnosis of Cardiac Transthyretin Amyloidosis

4. Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation inalpha2‐macroglobulinandtau: A population‐based autopsy study

5. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction

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