Literature DB >> 31378327

Inherited Cardiac Arrhythmias and Channelopathies.

Jessica Kline1, Otto Costantini2.   

Abstract

With recent advances in genetic diagnostics, many inherited diseases, which can cause life-threatening arrhythmias, are being better characterized. Many of these diseases are caused by genetic disorders that affect the function of the ion channels that regulate the action potential or the function of important cardiac muscle regulatory proteins. This article summarizes the diseases that we have learned about, such as the long QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. The article examines the diagnosis, genetic screening of patients and their relatives, management, and referral to a specialist for further therapy.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Brugada syndrome; Catecholaminergic polymorphic ventricular tachycardia; Channelopathies; Inherited cardiac arrhythmias; Long QT syndrome; Short QT syndrome

Mesh:

Year:  2019        PMID: 31378327     DOI: 10.1016/j.mcna.2019.05.001

Source DB:  PubMed          Journal:  Med Clin North Am        ISSN: 0025-7125            Impact factor:   5.456


  7 in total

1.  Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy.

Authors:  Hanife Saat; İbrahim Şahin; Haktan Bağış Erdem; Senem Özgür; Semiha Terlemez Tokgöz; Taha Bahsi
Journal:  Anatol J Cardiol       Date:  2022-06       Impact factor: 1.475

2.  Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years.

Authors:  Alexandre Janin; Louis Januel; Cécile Cazeneuve; Antoine Delinière; Philippe Chevalier; Gilles Millat
Journal:  Mol Diagn Ther       Date:  2021-05-05       Impact factor: 4.074

Review 3.  Human pluripotent stem cell-based cardiovascular disease modeling and drug discovery.

Authors:  Ge Liu; Zhun Liu; Nan Cao
Journal:  Pflugers Arch       Date:  2021-03-08       Impact factor: 3.657

Review 4.  Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

Authors:  Oscar Campuzano; Georgia Sarquella-Brugada; Sergi Cesar; Elena Arbelo; Josep Brugada; Ramon Brugada
Journal:  Int J Mol Sci       Date:  2020-09-28       Impact factor: 5.923

Review 5.  Drug Development and the Use of Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Disease Modeling and Drug Toxicity Screening.

Authors:  Paz Ovics; Danielle Regev; Polina Baskin; Mor Davidor; Yuval Shemer; Shunit Neeman; Yael Ben-Haim; Ofer Binah
Journal:  Int J Mol Sci       Date:  2020-10-03       Impact factor: 5.923

Review 6.  Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.

Authors:  Estefanía Martínez-Barrios; Sergi Cesar; José Cruzalegui; Clara Hernandez; Elena Arbelo; Victoria Fiol; Josep Brugada; Ramon Brugada; Oscar Campuzano; Georgia Sarquella-Brugada
Journal:  Biomedicines       Date:  2022-01-05

Review 7.  Ion Channels and Transporters in Muscle Cell Differentiation.

Authors:  Lingye Chen; Fatemeh Hassani Nia; Tobias Stauber
Journal:  Int J Mol Sci       Date:  2021-12-19       Impact factor: 5.923

  7 in total

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