Results 151 to 160 of about 25,737 (250)

Complex genetic background in a large family with Brugada syndrome [PDF]

, 2015
Siamak Saber, Mohamed‐Yassine Amarouch, Amirfarjam Fazelifar, Majid Haghjoo, Zahra Emkanjoo, Abolfath Alizadeh, Massoud Houshmand, Alexander V. Gavrilenko, Hugues Abriel, E. V. Zaklyazminskaya   +9 more
openalex   +1 more source

Brugada syndrome: a fatal disease with complex genetic etiologies – still a long way to go [PDF]

, 2017
Yang Wu, Mei Ai, Adham Sameer A. Bardeesi, Lunwu Xu, Jingjing Zheng, Da Zheng, Kun Yin, Qiuping Wu, Liyong Zhang, Lei Huang, Jianding Cheng   +10 more
openalex   +1 more source

[Brugada's syndrome].

Archivos de cardiologia de Mexico, 2002
The Brugada syndrome is an arrhythmic syndrome characterized by a right bundle branch block pattern and an segment elevation in the right precordial leads of the electrocardiogram, in conjunction with a high incidence of sudden death secondary to ventricular tachyarrhythmias. No evidence of structural heart disease is noted during diagnostic evaluation
openaire   +1 more source

The loss-of-function variant p.M764R in the cardiac sodium channel Nav1.5 is associated with ventricular arrhythmias and sudden cardiac death in a family without overt Brugada syndrome [PDF]

, 2023
Kirstine Calløe, Morten Krogh Christiansen, Finn Lund Henriksen, Henrik Kjærulf Jensen   +3 more
openalex   +1 more source

Impact of physical activity on presentation and prognosis of Brugada syndrome. [PDF]

Open Heart
Fernandez Gil MJ, Carrillo Mora LM, Fernandez Vazquez D, Melgarejo F, Santos Mateo JJ, Muñoz Esparza C, Rodriguez Serrano AI, Navarro-Penalver M, Sanchez Muñoz JJ, Gimeno-Blanes FJ, Sabater-Molina M, Gimeno JR.   +11 more
europepmc   +1 more source

Brugada syndrome

, 2023
In 1992, the Brugada brothers, Pedro and Josep, made a groundbreaking discovery by describing a previously unknown clinical condition that exhibited distinctive features such as right bundle branch block, persistent ST-segment elevation and sudden cardiac death in eight patients.
openaire   +1 more source

Current perspectives on risk prediction and genetic basis of Brugada syndrome. [PDF]

Front Cardiovasc Med
Bhardwaj P, Stavnem D, Jacobsen SB, Winkel BG, Tfelt-Hansen J.   +4 more
europepmc   +1 more source

SCN5A p.R965C in Brugada Syndrome: Effect of Nanomolecular Change

, 2021
Sora Yasri, Viroj Wiwanitkit, B Malik, A Ali Rudwan, M Abdelghani, M Mohsen, S Khan, N Aljefairi, E Mahmoud, N Asaad, S Hayat, O Campuzano, G Sarquella-Brugada, S Cesar, E Arbelo, J Brugada, R Brugada, S Roomi, W Ullah, H Abbas, H Abdullah, U Talib, V Figueredo, A Sarcon, H Hsia, P Postema, A Wilde, B Patocskai, J Di Diego, C Antzelevitch, M Scheinman, E Behr, Y Ben-Haim, M Ackerman, A Krahn, A Wilde, A Prez-Agustn, M Pinsach-Abuin, S Pagans, Y Kim, S Oh, H Choi, J Choi, C Brugada-Terradellas, A Hellemans, P Brugada, P Smets, J Isbister, N Nowak, A Butters, L Yeates, B Gray, R Sy, J Ingles, R Bagnall, C Semsarian, P Rattanawong, J Kewcharoen, C Kanitsoraphan, T Barry, A Shanbhag, N Ko Ko, W Vutthikraivit, M Home, P Agasthi, H Ashraf, W Shimizu, W Shen, V Wiwanitkit, V Wiwanitkit, A Wilde, A Amin, A Tamene, S Sattiraju, K Wang, D Benditt, S Yasri, V Wiwanitkit, B Joob, V Wiwanitkit, S Yasri, V Wiwanitkit, E Landa, S Sharifi, J Abraham, E Vigandt, E Munzinger, J Monterrubio-Villar, D Llinares-Moya, W Li, L Yin, C Shen, K Hu, J Ge, A Sun   +94 more
openalex   +1 more source

Multidisciplinary care of kidney donation in Brugada syndrome: A case report. [PDF]

World J Transplant
Khalil MAM, Rajput AS, Khalil MSU, Ullah SR, Ghani R, Daiwajna RG, Hong LK, Tan J.   +7 more
europepmc   +1 more source

Transcranial Magnetic Stimulation as an Antidepressant Alternative in a Patient With Brugada Syndrome and Recurrent Syncope [PDF]

, 2014
Miguel M. Alampay, Mark C. Haigney, M. Casey Flanagan, Robert M. Perito, Kathleen Love, Geoffrey Grammer   +5 more
openalex   +1 more source