Lone Atrial Fibrillation: Influence of Familial Disease on Gender Predilection
Open Access
- 22 July 2008
- journal article
- Published by Wiley in Journal of Cardiovascular Electrophysiology
- Vol. 19 (8) , 802-806
- https://doi.org/10.1111/j.1540-8167.2008.01126.x
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Long-Term Progression and Outcomes With Aging in Patients With Lone Atrial FibrillationCirculation, 2007
- ACC/AHA/ESC 2006 guidelines for the management of patients with atrial fibrillation: full text: A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients With Atrial Fibrillation) Developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm SocietyEP Europace, 2006
- ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial FibrillationCirculation, 2006
- Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillationHuman Molecular Genetics, 2006
- Heart Disease and Stroke Statistics—2006 UpdateCirculation, 2006
- Clinical Subtypes of Lone Atrial FibrillationPacing and Clinical Electrophysiology, 2005
- A Kir2.1 gain-of-function mutation underlies familial atrial fibrillationBiochemical and Biophysical Research Communications, 2005
- Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial FibrillationAmerican Journal of Human Genetics, 2004
- KCNQ1 Gain-of-Function Mutation in Familial Atrial FibrillationScience, 2003
- The Natural History of Lone Atrial FibrillationNew England Journal of Medicine, 1987