Familial Ventricular Tachycardia Latest Advances
Find the Latest Research About Familial Ventricular Tachycardia
Last Updated: 04/28/2026
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Found 452 publications
Red Flags for Differentiating Desmosomal "Hot-Phase" Cardiomyopathy From Acute Myocarditis.
Journal: Journal of the American Heart Association
Published: April 07, 2026
Psychiatric Medications and QTc Prolongation in the Pediatric Population.
Journal: Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent
Published: March 27, 2026
Inappropriate shocks from subcutaneous and transvenous implantable cardioverter-defibrillators: Reports from the FDA MAUDE database.
Journal: Heart rhythm O2
Published: February 25, 2026
Human-engineered heart tissues recapitulate tissue-scale mechanisms underlying ventricular tachycardia.
Journal: bioRxiv : the preprint server for biology
Published: February 23, 2026
The Long-Term Clinical Progression of Genotype-Positive/Phenotype-Negative Patients With Hypertrophic Cardiomyopathy.
Journal: The American journal of cardiology
Published: January 12, 2026
Novel Use of Helium Insufflation to Facilitate Epicardial Access in Ventricular Tachycardia Ablation.
Journal: Journal of cardiovascular electrophysiology
Published: January 08, 2026
Mitral Annular Disjunction Presenting With Ventricular Arrhythmia: A Case Report.
Journal: Cureus
Published: December 14, 2025
Breaking the Rhythm: Extracorporeal Membrane Oxygenation (ECMO) as a Life Saver in a Case of Resistant Arrhythmia and Cardiac Arrest.
Journal: Cureus
Published: December 14, 2025
Homozygous and heterozygous penetrance of a missense CASQ2 variant in a South Asian family.
Journal: HeartRhythm case reports
Published: December 03, 2025
STAR Power: Noninvasive Radiation Therapy for Ventricular Tachycardia Enters a New Era.
Journal: International journal of radiation oncology, biology, physics
Published: December 03, 2025
Generation of three heterozygous and two homozygous hiPSC lines from a CPVT associated mutation RYR2_p.G357S from a large family of the Canary Islands.
Journal: Stem cell research
Published: December 01, 2025
Last Updated: 04/28/2026