Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection-Reference-Cited by-同舟云学术

Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection

Published:2020-03-06 Issue:3 Volume:7 Page:1338-1343
ISSN:2055-5822
Container-title:ESC Heart Failure
language:en
Short-container-title:ESC Heart Failure

Author:

Tamiya Ran¹,Saito Yuki¹,Fukamachi Daisuke¹,Nagashima Koichi¹,Aizawa Yoshihiro¹,Ohkubo Kimie¹,Hatta Takumi¹,Sezai Akira²,Tanaka Masashi²,Ishikawa Taisuke³,Makita Naomasa³,Sumitomo Naokata⁴,Okumura Yasuo¹

Affiliation:

1. Division of Cardiology, Department of Medicine Nihon University School of Medicine 30‐1 Ohyaguchi‐kamicho, Itabashi‐ku Tokyo 173‐8610 Japan

2. Department of Cardiovascular Surgery Nihon University School of Medicine Tokyo Japan

3. Omics Research Center, National Cerebral and Cardiovascular Center Suita Japan

4. Department of Pediatric Cardiology Saitama Medical University International Medical Center Saitama Japan

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ehf2.12667

Reference14 articles.

1. Molecular insights into cardiomyopathies associated with desmin (DES) mutations

2. Prevalence of Desmin Mutations in Dilated Cardiomyopathy

3. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

4. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

5. The Promise and Peril of Precision Medicine

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2. Structural and signaling proteins in the Z-disk and their role in cardiomyopathies;Frontiers in Physiology;2023-03-02

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4. Case report: An unusual case of desmin myopathy associated with heart failure and arrhythmia;Frontiers in Cardiovascular Medicine;2022-07-25

5. Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with SPEG Compound Heterozygous Variants;International Journal of Molecular Sciences;2022-05-06