Log in to save to my catalogue

Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes

Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5798fb14b4f8450e944d64feb174d8ff

Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes

About this item

Full title

Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes

Publisher

England: Radcliffe Medical Education Ltd

Journal title

Arrhythmia & electrophysiology review, 2019-05, Vol.8 (2), p.122-130

Language

English

Formats

Publication information

Publisher

England: Radcliffe Medical Education Ltd

More information

Scope and Contents

Contents

Congenital long QT syndrome (LQTS) has been the most investigated cardiac ion channelopathy. Although congenital LQTS remains the domain of cardiologists, cardiac electrophysiologists and specialised centres, the much more frequently acquired LQTS is the domain of physicians and other members of healthcare teams required to make therapeutic decisio...

Alternative Titles

Full title

Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_5798fb14b4f8450e944d64feb174d8ff

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5798fb14b4f8450e944d64feb174d8ff

Other Identifiers

ISSN

2050-3369

E-ISSN

2050-3377

DOI

10.15420/aer.2019.8.3

How to access this item