Results 61 to 70 of about 5,972 (163)

Current Topics of Progressive Cardiac Conduction Disease

open access: yesJournal of Arrhythmia, Volume 42, Issue 3, June 2026.
Many genes and the protein cause PCCD. Mutation of NaV1.5 or CX40 cause isolated PCCD, but mutation of lamin A/C, emerin, or desmin lead to cardiomyopathy, and PCCD. Mutation of transcription factor NCX2‐5, and Tbx5 associated with atrial septal defect and abnormal development of conduction system.
Naokata Sumitomo   +7 more
wiley   +1 more source

Ivabradine and endothelium: an update

open access: yesTherapeutic Advances in Cardiovascular Disease, 2020
Ivabradine is a pure heart-rate lowering drug that is nowadays used, accordingly to the last ESC Guidelines, to reduce mortality and heart failure (HF) hospitalization in patients with HF with reduced ejection fraction and in symptomatic patiens with ...
Lucia Dallapellegrina   +2 more
doaj   +1 more source

Open‐Window Mapping for Accessory Pathway Ablation: Influence of Catheter Design on Mapping Performance

open access: yesJournal of Arrhythmia, Volume 42, Issue 3, June 2026.
8‐spline high‐density open‐window mapping achieved higher spatial resolution, sharper EEML‐defined accessory pathway gap delineation, and shorter mapping time compared with 5‐spline catheters, and was associated with higher first‐pass ablation success, supporting improved mapping‐guided targeting precision in Wolff–Parkinson–White syndrome.
Kazuma Iimura   +5 more
wiley   +1 more source

Catastrophic implantable cardioverter-defibrillator misclassification of ventricular tachycardia

open access: yesEuropean Journal of Case Reports in Internal Medicine
Inappropriate therapy is a frequent adverse consequence of implantable cardioverter-defibrillator. Inappropriate therapy often occurs due to the misinterpretation of sinus tachycardia or atrial fibrillation/flutter with rapid atrioventricular conduction ...
Zhafran Veliawan   +3 more
doaj   +1 more source

Abnormal Ca2+ homeostasis, atrial arrhythmogenesis and sinus node dysfunction in murine hearts modelling RyR2 modification

open access: yesFrontiers in Physiology, 2013
RyR2 mutations are implicated in catecholaminergic polymorphic ventricular tachycardia thought to result from altered myocyte Ca2+ homeostasis reflecting inappropriate ‘leakiness’ of RyR2-Ca2+ release channels arising from increases in their basal ...
Yanmin eZhang   +5 more
doaj   +1 more source

Inappropriate Sinus Tachycardia: Etiology, Pathophysiology, and Management: JACC Review Topic of the Week.

open access: yesJournal of the American College of Cardiology, 2022
Inappropriate sinus tachycardia (IST) is a clinical syndrome that generally affects young patients and is associated with distressing symptoms. Although the most common symptom is palpitations, it can be accompanied by a myriad of symptoms, including anxiety, dizziness, presyncope, and syncope.
Ahmed, Adnan   +12 more
openaire   +2 more sources

Surgery for Cardiac Arrhythmias: Past, Present, Future

open access: yesRambam Maimonides Medical Journal
There is a rich history of surgery for cardiac arrhythmias, spanning from atrial fibrillation and Wolff–Parkinson–White syndrome to inappropriate sinus tachycardia and ventricular tachycardia.
Stephen D. Waterford, Niv Ad
doaj   +1 more source

Reply to the Editor - Maternal inappropriate sinus tachycardia during pregnancy. [PDF]

open access: yesHeart Rhythm O2, 2023
Prystowsky EN   +3 more
europepmc   +1 more source

A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family. [PDF]

open access: yesProc Natl Acad Sci U S A, 2023
Cámara-Checa A   +14 more
europepmc   +1 more source

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