Arrhythmogenic Cardiomyopathy and Skeletal Muscle Dystrophies: Shared Histopathological Features and Pathogenic Mechanisms-Reference-Cited by-同舟云学术

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Arrhythmogenic Cardiomyopathy and Skeletal Muscle Dystrophies: Shared Histopathological Features and Pathogenic Mechanisms

Published:2020-07-30 Issue: Volume:11 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Gao Shanshan,Chen Suet Nee,Di Nardo Carlo,Lombardi Raffaella

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

American Heart Association

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference163 articles.

1. Arrhythmogenic right ventricular cardiomyopathy with recessive inheritance related to a new homozygous desmocollin-2 mutation.;Al-Sabeq;Can. J. Cardiol.,2014

2. Monoclonal antibody analysis of mononuclear cells in myopathies. I: quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells.;Arahata;Ann. Neurol.,1984

3. Altered desmosomal proteins in granulomatous myocarditis and potential pathogenic links to arrhythmogenic right ventricular cardiomyopathy.;Asimaki;Circ. Arrhythm. Electrophysiol.,2011

4. A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy.;Asimaki;N Engl. J. Med.,2009

5. Changes in calsequestrin, TNF-alpha, TGF-beta and MyoD levels during the progression of skeletal muscle dystrophy in mdx mice: a comparative analysis of the quadriceps, diaphragm and intrinsic laryngeal muscles.;Barros Maranhao;Int. J. Exp. Pathol.,2015

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4. Extracellular vesicles from immortalized cardiosphere-derived cells attenuate arrhythmogenic cardiomyopathy in desmoglein-2 mutant mice;European Heart Journal;2021-07-29

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