Results 31 to 40 of about 25,737 (250)

Enhancing rare cardiac disease classification with GAN-augmented supervised and self-supervised learning: a case study on Brugada syndrome [PDF]

Eur Heart J Digit Health
B Zanchi, G Monachino, G Conte, F Faraci
europepmc   +2 more sources

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

, 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, Aydin A, Bahring S, Dahm S, Guenthe, Bezzina C, Veldkamp MW, van Den Ber, Brugada P and Brugada J, Chen JZ, Xie XD, Wang XX, Tao M, Sh, Furuhashi M, Uno K, Tsuchihashi K,, Huang H, Zhao J, Barrane FZ, Champa, Splawski I, Shen J, Timothy KW, Leh, Wattanasirichaigoon D, Vesely MR, D   +8 more
core   +1 more source

Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations

Journal of Biomedical Science, 2009
The Brugada syndrome is characterized by ST segment elevation in the right precodial leads V1-V3 on surface ECG accompanied by episodes of ventricular fibrillation causing syncope or even sudden death.
Juang Jyh-Ming, Liu Yen-Bin, Tsai Chia-Ti, Lin Jiunn-Lee, Chen Wen-Pin, Hsueh Chia-Hsiang, Tsao Hsuan-Ming, Su Ming-Jai, Lai Ling-Ping   +8 more
doaj   +1 more source

Brugada Syndrome: Presentation and Management of the Atypical Patient in the Emergent Setting [PDF]

, 2020
Introduction: Brugada syndrome is a genetic disorder of the heart’s electrical system that increases a patient’s risk of sudden cardiac death. It is a syndrome most prevalent in Southeast Asians and is found 36 times more commonly in Asians than in ...
Flores, Mario, Nguyen, Alexander, Tano, Vilmogil   +2 more
core  

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

, 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, Guo, Leydesdorff, Leydesdorff, Lundberg, Ohniwa, Stegmann, Torvik, Wickham   +8 more
core   +2 more sources

BRUGADA SYNDROME: FROM PRIMARY ELECTRIC HEART DISEASE TO MORPHOLOGICAL SUBSTRATE

Архивъ внутренней медицины, 2016
Nowadays interest in channelopathies is growing, and developing diagnostic capabilities make Brugada syndrome much more actual problem than ever. Conception of «primary electric heart disease», which earlier was so popular, now couldn’t explain the ...
T. A. Pavlenko, O. V. Blagova
doaj   +1 more source

Padrão de Brugada em doente medicada com lamotrigina

Revista Portuguesa de Cardiologia, 2013
Resumo: Os autores relatam o caso de uma mulher de 52 anos com síndrome depressiva, medicada com lamotrigina há cerca de cinco meses, que recorre à urgência por dor pré-cordial atípica.
Rita Rodrigues, Pedro Amador, Leandro Rassi, Filipe Seixo, Leonor Parreira, Nuno Fonseca, Luís Soares   +6 more
doaj   +1 more source

Shortening of the Short Refractory Periods in Short QT Syndrome. [PDF]

, 2017
BACKGROUND: Diagnosis of short QT syndrome (SQTS) remains difficult in case of borderline QT values as often found in normal populations. Whether some shortening of refractory periods (RP) may help in differentiating SQTS from normal subjects is unknown.
Cardin, C, Fourcade, C, Gaita, F, Gandjbakhch, E, Giustetto, C, Maupain, C, Maury, P, Mondoly, P, Monteil, B, Rollin, A, Scrocco, C   +10 more
core   +3 more sources

The Advances in Diagnosis and Treatment of Brugada Syndrome: A Comprehensive Review

Quality in Sport
Introduction: Brugada Syndrome (BrS) is a rare genetic cardiac disorder that predisposes individuals to ventricular fibrillation and sudden cardiac death, often without structural heart disease.
Bartosz Szepietowski, Wiktoria Mączyńska, Justyna Dutkiewicz, Michał Wijata, Anna Maria Wijata, Zuzanna Adriana Przybyłek-Stępień, Ryszard Bartosiński, Jan Szustak, Maria Kąpa, Jakub Marek Kaźmierczak, Ewelina Rycerz, Piotr Pasek   +11 more
doaj   +1 more source

The Brugada Syndrome

Cardiac Electrophysiology Review, 1999
The Brugada syndrome is a genetically determined disease caused by mutations of the cardiac sodium channel. The disease affects mainly males in their forties and causes sudden cardiac death because of polymorphic ventricular tachycardia. These patients have a structurally normal heart.
Brugada, Pedro, Brugada, J., Brugada, R.
openaire   +5 more sources