Results 21 to 30 of about 4,801 (176)

PRKAG2 and PRKAG3 genes in patients with Wolff-Parkinson-White syndrome: a literature review

open access: yesРоссийский кардиологический журнал, 2023
Wolff-Parkinson-White syndrome (WPW) is a syndrome with early ventricular excitation due to the abnormal electrical conduction through an accessory atrioventricular pathway, and is usually accompanied by supraventricular tachycardia.
Yu. A. Tolstokorova   +4 more
doaj   +1 more source

Wolff-Parkinson-White Syndrome: Electrocardiogram

open access: yesJournal of Education and Teaching in Emergency Medicine, 2016
History of present illness: A 26-year-old male with no significant past medical history presented to the emergency department with palpitations. The patient experienced these symptoms five times before in his life, but they had self-resolved with ...
Brianna Miner   +2 more
doaj   +1 more source

Multiple Cardiac Rhabdomyomas, Wolff-Parkinson-White Syndrome, and Tuberous Sclerosis: An Infrequent Combination

open access: yesCase Reports in Pediatrics, 2014
Cardiac rhabdomyomas are benign cardiac tumours and are often associated with tuberous sclerosis. They are often asymptomatic with spontaneus regresion but can cause heart failure, arrhythmias, and obstruction. There have also been a few isolated reports
Elena Castilla Cabanes   +1 more
doaj   +1 more source

Association of olfactory neuropathy spectrum disorder and Wolff‐Parkinson‐White syndrome: A Report of a case

open access: yesClinical Case Reports, 2020
Olfactory neuropathy spectrum disorder is characterized by hyposmia or anosmia and hypoplastic or absent olfactory bulbs. There may be an association between olfactory neuropathy spectrum disorder and Wolff‐Parkinson‐White syndrome.
Mitchell R. Gore
doaj   +1 more source

Hypertrophic Cardiomyopathy and Wolff-Parkinson-White Syndrome in a Young African Soldier with Recurrent Syncope

open access: yesCase Reports in Cardiology, 2019
Syncope is a common manifestation of both hypertrophic cardiomyopathy (HCM) and Wolff-Parkinson-White (WPW) syndrome. The most common arrhythmia in HCM is ventricular tachycardia (VT) and atrial fibrillation (AF).
Mohammed Abdullahi Talle   +3 more
doaj   +1 more source

The coexistence of Wolff-Parkinson-White syndrome (WPW) and atrioventricular nodal reentrant tachycardia (AVNRT)

open access: yesTurkish Journal of Emergency Medicine, 2018
Atrioventricular nodal reentrant tachycardia (AVNRT) is the most common type of reentrant paroxysmal supraventricular tachycardia that occurs in the presence of dual AV nodal physiology.
Ali Elitok   +4 more
doaj   +1 more source

Left ventricular noncompactation and pre-excitation: an unusual finding in adults

open access: yesClinical and Biomedical Research, 2017
Left ventricular noncompaction (LVNC) is a rare form of cardiomyopathy characterized by prominent left ventricular (LV) trabeculae, deep intertrabecular recesses, and the thin compacted layer.
Diego Chemello, Fernando Pivatto Júnior
doaj   +2 more sources

Utility of unipolar recordings for complex Wolff–Parkinson–White ablation

open access: yesIndian Pacing and Electrophysiology Journal, 2015
Radiofrequency ablation has been shown to be a safe and effective treatment strategy for the management of symptomatic patients with Wolff–Parkinson–White syndrome. It is supported by a success rate of 95% and a recurrence rate of less than 5%.
Ponnusamy Shunmuga Sundaram, Jasbir Sra
doaj   +1 more source

Repolarization adaptation to rapid change in heart rate in human models – a review

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend This review focuses on non‐invasive assessment of repolarization duration and dispersion (heterogeneity) adaptation to change in heart rate (HR). HR was increased incrementally by left atrial pacing during an electrophysiology (EP) study and by a bolus injection of atropine and in a step up/down fashion by repeated right atrial ...
Lennart Bergfeldt   +5 more
wiley   +1 more source

Expanding the Phenotype of TUFM ‐Related Combined Oxidative Phosphorylation Deficiency 4

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1884-1889, August 2026.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier   +2 more
wiley   +1 more source

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