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Arrhythmogenic channelopathy syndromes presenting as refractory epilepsy
Matthew A. Hazle
,
Renée A. Shellhaas
, David J. Bradley
, Macdonald Dick
, Martin J. Lapage
Department of Neurology
School of Medicine
Research output
:
Contribution to journal
›
Article
›
peer-review
16
Scopus citations
Overview
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Keyphrases
Refractory Epilepsy
100%
Cardiac Channelopathies
100%
Channelopathy
100%
Syncope
66%
Older Adults
33%
Pathophysiology
33%
Clinical Features
33%
Seizure
33%
Improved Outcomes
33%
Medical Care
33%
Medical Management
33%
Ventricular Arrhythmia
33%
Long QT Syndrome
33%
Cerebral Hypoperfusion
33%
Catecholaminergic Polymorphic Ventricular Tachycardia
33%
Refractory Seizures
33%
Convulsive Syncope
33%
Genetic Arrhythmia Syndromes
33%
Pharmacology, Toxicology and Pharmaceutical Science
Syndrome
100%
Faintness
100%
Channelopathy
100%
Intractable Epilepsy
100%
Drug Resistant Epilepsy
100%
Cardiac Channelopathy
100%
Pathophysiology
33%
Heart Arrhythmia
33%
Clinical Feature
33%
Heart Ventricle Arrhythmia
33%
Long QT Syndrome
33%
Catecholaminergic Polymorphic Ventricular Tachycardia
33%