LONG QT SYNDROME
- 1 May 2000
- journal article
- review article
- Published by Elsevier BV in Cardiology Clinics
- Vol. 18 (2), 309-325
- https://doi.org/10.1016/s0733-8651(05)70143-0
Abstract
No abstract availableKeywords
This publication has 77 references indexed in Scilit:
- MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac ArrhythmiaCell, 1999
- Optical Mapping of Drug-Induced Polymorphic Arrhythmias and Torsade de Pointes in the Isolated Rabbit HeartJournal of the American College of Cardiology, 1997
- Mechanisms in Adrenergic Dependent Onset of Torsades de PointesPacing and Clinical Electrophysiology, 1997
- KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium currentNature, 1996
- Genetically Defined Therapy of Inherited Long-QT SyndromeCirculation, 1996
- Molecular mechanism for an inherited cardiac arrhythmiaNature, 1995
- Role of M cells in acquired long QT syndrome, U waves, and torsade de pointesJournal of Electrocardiology, 1995
- Nicorandil Suppresses a Hump on the Monophasic Action Potential and Torsade de Pointes in a Patient with Idiopathic Long QT Syndrome.Japanese Heart Journal, 1995
- Clinical relevance of cardiac arrhythmias generated by afterdepolarizationsJournal of the American College of Cardiology, 1994
- Efficacy of left cardiac sympathectomy in the treatment of patients with the long QT syndrome.Cell Metabolism, 1984