Results 31 to 40 of about 25,250 (236)

International criteria for electrocardiographic interpretation in athletes: Consensus statement. [PDF]

open access: yes, 2017
Sudden cardiac death (SCD) is the leading cause of mortality in athletes during sport. A variety of mostly hereditary, structural or electrical cardiac disorders are associated with SCD in young athletes, the majority of which can be identified or ...
Aagaard   +198 more
core   +2 more sources

Brugada syndrome with a novel missense mutation in SCN5A gene: A case report from Bangladesh

open access: yesIndian Heart Journal, 2014
Brugada syndrome is an inherited cardiac arrhythmia that follows autosomal dominant transmission and can cause sudden death. We report a case of Brugada syndrome in a 55-year-old male patient presented with recurrent palpitation, atypical chest pain and ...
Md. Zahidus Sayeed   +3 more
doaj   +1 more source

Unmasking of Brugada syndrome by lamotrigine in a patient with pre-existing epilepsy: A case report with review of the literature

open access: yesFrontiers in Cardiovascular Medicine, 2022
Brugada syndrome is an inherited cardiac channelopathy arising from mutations in voltage-gated cardiac sodium channels. Idiopathic epilepsy portrays a coalescent underlying pathophysiological mechanism pertaining to the premature excitation of neuronal ...
Hafiz Omer   +8 more
doaj   +1 more source

Teaching a Machine to Diagnose a Heart Disease; Beginning from digitizing scanned ECGs to detecting the Brugada Syndrome (BrS) [PDF]

open access: yesarXiv, 2020
Medical diagnoses can shape and change the life of a person drastically. Therefore, it is always best advised to collect as much evidence as possible to be certain about the diagnosis. Unfortunately, in the case of the Brugada Syndrome (BrS), a rare and inherited heart disease, only one diagnostic criterion exists, namely, a typical pattern in the ...
arxiv  

Robust Syndrome Extraction via BCH Encoding [PDF]

open access: yesarXiv, 2023
Quantum data-syndrome (QDS) codes are a class of quantum error-correcting codes that protect against errors both on the data qubits and on the syndrome itself via redundant measurement of stabilizer group elements. One way to define a QDS code is to choose a syndrome measurement code, a classical block code that encodes the syndrome of the underlying ...
arxiv  

Clinical Features of Brugada Syndrome Patients With SCN5A Variants

open access: yesJournal of Cardiovascular Electrophysiology, EarlyView.
Longer r‐J interval in lead V1, fragmented QRS and carrying SCN5A variants other than benign variants are independently associated with the cardiac events in BrS patients. LAS40 and RMS40 are useful for the risk stratification in BrS patients with SCN5A VUS or pathogenic variants.
Sho Okamura   +13 more
wiley   +1 more source

Matching MEDLINE/PubMed data with Web of Science (WoS): a routine in R language [PDF]

open access: yes, 2014
We present a novel routine, namely medlineR, based on R language, that enables the user to match data from MEDLINE/PubMed with records indexed in the ISI Web of Science (WoS) database.
Boyack   +8 more
core   +2 more sources

Fainting Spells

open access: yesJournal of Education and Teaching in Emergency Medicine, 2018
Audience: The target audience for this simulation is 4th year medical students, emergency medicine residents, pediatric residents, and family medicine residents.
Brittany Guest, DO   +2 more
doaj   +1 more source

Fascicular/Purkinje Tissue Colocalized With Scar in Cardiomyopathy Patients Undergoing Ventricular Fibrillation Ablation

open access: yesPacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Background Ventricular fibrillation (VF) is a poorly understood arrhythmia that is one of the main mechanisms of sudden cardiac death in patients with structural heart disease (SHD). Fascicular and Purkinje tissue (FPT) has been implicated in VF.
Emir Baskovski   +8 more
wiley   +1 more source

Mutations and SNPs of human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese patients with Brugada syndrome [PDF]

open access: yes, 2007
Background: Brugada syndrome is an inherited arrhythmogenic disease characterized by right bundle branch block pattern and ST segment elevation, leading to the change of V1 to V3 on electrocardiogram, and an increased risk of sudden cardiac death ...
Ackerman MJ, Splawski I, Makielski   +8 more
core   +1 more source

Home - About - Disclaimer - Privacy