LMNA-Mediated Arrhythmogenic Right Ventricular Cardiomyopathy and Charcot-Marie-Tooth Type 2B1: A Patient-Discovered Unifying Diagnosis-Reference-Cited by-同舟云学术

LMNA-Mediated Arrhythmogenic Right Ventricular Cardiomyopathy and Charcot-Marie-Tooth Type 2B1: A Patient-Discovered Unifying Diagnosis

Published:2016-05-31 Issue:7 Volume:27 Page:868-871
ISSN:1045-3873
Container-title:Journal of Cardiovascular Electrophysiology
language:en
Short-container-title:J Cardiovasc Electrophysiol

Author:

LIANG JACKSON J.¹²,GOODSELL KIM,GROGAN MARTHA¹,ACKERMAN MICHAEL J.¹³⁴

Affiliation:

1. Division of Heart Rhythm Services, Department of Cardiovascular Diseases; Hospital of the University of Pennsylvania; Philadelphia Pennsylvania USA

2. Division of Cardiology; Hospital of the University of Pennsylvania; Philadelphia Pennsylvania USA

3. Division of Pediatric Cardiology, Department of Pediatrics; Hospital of the University of Pennsylvania; Philadelphia Pennsylvania USA

4. Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory; Hospital of the University of Pennsylvania; Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jce.12984/fullpdf

Reference19 articles.

1. Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy;Quarta;Eur Heart J,2012

2. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed modification of the Task Force Criteria;Marcus;Circulation,2010

3. Right ventricular cardiomyopathy and sudden death in young people;Thiene;N Engl J Med,1988

4. Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology;McKenna;Br Heart J,1994

5. Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene;Tintelen;Heart Rhythm,2009

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Epigenetics in LMNA-Related Cardiomyopathy;Cells;2023-03-01

2. Big Data Analytics in Healthcare;Translational Systems Sciences;2023

3. The role of inner nuclear membrane proteins in tumourigenesis and as potential targets for cancer therapy;Cancer and Metastasis Reviews;2022-10-07

4. Dilated cardiomyopathy and chronic cardiac inflammation: Pathogenesis, diagnosis and therapy;Journal of Internal Medicine;2022-08-27

5. Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality;Orphanet Journal of Rare Diseases;2022-05-07