Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure-Reference-Cited by-同舟云学术

Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure

Published:2021-09-06 Issue:6 Volume:8 Page:5178-5191
ISSN:2055-5822
Container-title:ESC Heart Failure
language:en
Short-container-title:ESC Heart Failure

Author:

Saito Tsunenori¹²^ORCID,Sato Naoko Saito³,Mozawa Kosuke²,Adachi Akiko⁴,Sasaki Yoshihiro⁴,Nakamura Kotoka¹,Oka Eiichiro²,Otsuka Toshiaki⁵,Kodani Eitaro⁶,Asai Kuniya⁷,Mizuno Kyoichi²,Shimizu Wataru²,Gottlieb Roberta A.¹

Affiliation:

1. Smidt Heart Institute Cedars‐Sinai Medical Center 8700 Beverly Blvd Los Angeles CA 90048 USA

2. Department of Cardiovascular Medicine Nippon Medical School Graduate School Tokyo Japan

3. Department of Neurology Japanese Red Cross Medical Center Tokyo Japan

4. Division of Morphological and Biomolecular Research, Graduate School of Medicine Nippon Medical School Tokyo Japan

5. Department of Hygiene and Public Health Nippon Medical School Graduate School Tokyo Japan

6. Department of Internal Medicine and Cardiology Nippon Medical School Tama Nagayama Hospital Tokyo Japan

7. Intensive Care Unit Nippon Medical School Chiba Hokusoh Hospital Chiba Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ehf2.13596

Reference26 articles.

1. Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

2. Prevalence and Prognostic Significance of Left Ventricular Reverse Remodeling in Dilated Cardiomyopathy Receiving Tailored Medical Treatment

3. Truncations of Titin Causing Dilated Cardiomyopathy

4. Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

5. Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy

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