Results 41 to 50 of about 23,889 (287)

Rapid wide QRS tachycardia with an unknown cause

open access: yesAnnals of Noninvasive Electrocardiology, 2022
One‐to‐one atrioventricular conduction during atrial flutter is one of the most severe life‐threatening arrhythmias and is hemodynamically perilous. Rapid wide QRS tachycardia often not only occurs in patients with ventricular tachycardia but is also ...
Dalong Hu, Jingxiu Li
doaj   +1 more source

Transient complete heart block following catheter ablation of a left lateral accessory pathway. [PDF]

open access: yes, 2019
A 16-year-old female with symptomatic Wolff-Parkinson-White (WPW) syndrome underwent catheter ablation of a left-sided lateral accessory pathway. The accessory pathway was eliminated with the first ablation lesion; however, the patient immediately ...
Birgersdotter-Green, Ulrika   +5 more
core   +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

Wolff-parkinson-white syndrome: Long follow-up and an anglo-american historical note [PDF]

open access: yes, 1983
A patient who developed palpitation in 1917 was later found to have the Wolff-Parkinson-White syndrome and survived to the age of 86, when he died of emphysema.
Krikler, Dennis M.
core   +1 more source

Cardiac manifestations of PRKAG2 mutation. [PDF]

open access: yes, 2018
BACKGROUND:The Protein Kinase AMP-Activated Non-Catalytic Subunit Gamma 2 (PRKAG2) cardiac syndrome is characterized by glycogen accumulation in the cardiac tissue.
Ardehali, Reza   +3 more
core   +1 more source

The natural history of Wolff-Parkinson-White syndrome in 228 military aviators: a long-term follow-up of 22 years.

open access: yesAmerican Heart Journal, 2001
BACKGROUND Wolff-Parkinson-White (WPW) syndrome poses a risk for tachyarrhythmias and sudden cardiac death. Most WPW studies have relatively limited numbers of subjects and brief follow-up periods.
Patrick J. Fitzsimmons   +3 more
semanticscholar   +1 more source

Síndrome de Wolff-Parkinson-White associada a comunicação interatrial tipo seio venoso Wolff-Parkinson-White syndrome and the sinus venosus atrial septal defect association

open access: yesArquivos Brasileiros de Cardiologia, 2005
A associação de comunicação interatrial (CIA) tipo seio venoso com síndrome de Wolff Parkinson White (WPW) é muito rara e ainda não descrita na literatura médica especializada.
Patrícia Lopes Moraes   +4 more
doaj   +1 more source

998-61 Population Prevalence of Wolff-Parkinson-White Syndrome [PDF]

open access: yes, 1995
Little is known about the epidemiology of Wolff-Parkinson-White (WPW) syndrome in the general population. Virtually all previous studies have been either case series from tertiary care centers or limited to young adult males screened for military ...
DeStefano, Frank   +5 more
core   +1 more source

A randomized study of prophylactic catheter ablation in asymptomatic patients with the Wolff-Parkinson-White syndrome.

open access: yesNew England Journal of Medicine, 2003
BACKGROUND Young age and inducibility of atrioventricular reciprocating tachycardia or atrial fibrillation during invasive electrophysiological testing identify asymptomatic patients with a Wolff-Parkinson-White pattern on the electrocardiogram as being ...
C. Pappone   +11 more
semanticscholar   +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

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