Results 201 to 210 of about 829,629 (331)
Abstract Objective This study was undertaken to determine the incidence of sudden unexpected death in epilepsy (SUDEP) in New Zealand. Methods We attempted to prospectively identify all people with epilepsy (PWE) in New Zealand who died from SUDEP after August 1, 2019.
Peter S. Bergin+4 more
wiley +1 more source
Incidence of Rapid Rate Non-Sustained and Sustained Ventricular Tachycardia in Implantable Cardioverter-Defibrillator Recipients and Its Correlation With Heart Failure Guideline-Directed Medical Therapy Compliance. [PDF]
Khan MT+5 more
europepmc +1 more source
V. Luther+11 more
semanticscholar +1 more source
Abstract Objective Factors that can precipitate and/or prolong functional seizure events are often challenging to identify. We aimed to develop a methodology to investigate peri‐ictal behaviors in subjects experiencing functional seizures and those around them in their home environment. Methods We conducted an iterative, four‐phase process to develop a
Lana Higson+6 more
wiley +1 more source
Unusual catecholaminergic polymorphic ventricular tachycardia and bradycardia caused by a novel triadin variant in 2 siblings from a Malian family. [PDF]
Diakité M+13 more
europepmc +1 more source
Substrate mapping for unstable ventricular tachycardia.
P. Santangeli, F. Marchlinski
semanticscholar +1 more source
Abstract Epilepsy is a chronic neurological condition marked by recurrent, uncontrolled seizures. Identifying comorbidities in epilepsy is critical for preventing mortality. Among these, the autonomic nervous system's role in epilepsy often manifests as cardiac disorders. Patients with epilepsy (PWE), particularly those with poorly controlled seizures,
Enes Akyuz+2 more
wiley +1 more source
Saurabh Kumar+12 more
semanticscholar +1 more source
Abstract Objective Fibroblast growth factor 12 (FGF12), a member of the fibroblast homologous factor family, plays a key role in the modulation of voltage‐gated sodium (Nav) channels. Pathogenic variants in the FGF12 gene leading to a gain‐of‐function mechanism and partial duplication encompassing the FGF12 gene leading to a loss‐of‐function mechanism ...
Jade Fauqueux+18 more
wiley +1 more source