Results 111 to 120 of about 1,147,137 (221)

Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A

, 2020
Background: A 30-year-old man presented with intellectual disability associated with epilepsy. The epilepsy was initially treated with sodium valproate and since he was 28 years-old with lamotrigine. With the addition of lamotrigine, a pattern of Brugada
Banfi P., Oliva A., Princiotta L., Campuzano O., Brugada R., Striano P., Coll M., Versino M., Alcalde M., Mauri M.   +9 more
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Brugada syndrome - Report of the second consensus conference - Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association

, 2005
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being a rare disease to one that is second only to automobile accidents as a cause of death among young adults in some countries.
WILDE A., CORRADO, DOMENICO, BRUGADA J, GUSSAK I, BORGGREFE M, SCHULZE BAHR E, TAN H, NADEMANEE K, LEMAREC H, BRUGADA R, RIERA ARP, ANTZELEVITCH C, SHIMIZU W, BRUGADA P   +13 more
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Sudden Cause of Cardiac Death—Be Aware of Me: A Case Report and Short Review on Brugada Syndrome

Case Reports in Medicine, 2010
Introduction. Brugada syndrome accounts for about 4% of sudden cardiac deaths (SCD). It is characterized by an ST-segment elevation in the right precordial electrocardiogram (EKG) leads. Case Presentation. We describe a 39-year-old healthy Caucasian man
Jagadeesh K. Kalavakunta, Vishwaroop Bantu, Hemasri Tokala, Mihas Kodenchery   +3 more
doaj   +1 more source

Brugada syndrome, Brugada phenocopy or none?

, 2017
Brugada syndrome is a form of inherited arrhythmia syndrome characterized by a distinct ST-segment elevation in the right precordial leads. Brugada phenocopies are clinical entities that present with an electrocardiographic pattern identical to Brugada ...
Adrian Baranchuk, Cuneyt Turkoglu, Hasdemir, Can, Kaya, Esra, Baranchuk, Adrian, Can Hasdemir, Umut Kocabas, Kocabas, Umut, Esra Kaya, Turkoglu, Cuneyt   +9 more
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Brugada syndrome update

Frontiers in Physiology
Brugada syndrome (BrS), a genetic disorder affecting cardiac ion channels, predominantly manifests due to mutations that impair the function of the Nav1.5 sodium channel’s α-subunit. This condition, identified by Josep and Pedro Brugada, is often marked by symptoms such as syncope and episodes of polymorphic ventricular tachycardia (PVT) or ventricular
Tingting Xu, Shaokun Wang, Jiawen Wang, Jihong Xing   +3 more
openaire   +3 more sources

The Brugada Syndrome-An Update-

Internal Medicine, 2005
Brugada syndrome is characterized by ST-segment elevation in the right precordial leads (V1-V3) and an episode of ventricular fibrillation (VF) in the absence of structural heart disease. A number of reports from the world have unveiled the clinical, electrocardiographic, electrophysiologic and prognostic features of Brugada syndrome, and two recent ...
openaire   +3 more sources

Cardiac autonomic control in Brugada syndrome patients during sleep : the effects of sleep disordered breathing

, 2013
Aims Brugada syndrome is characterized by typical ECG features, ventricular arrhythmias and sudden cardiac death (SCD), more frequent during nighttime. Autonomic cardiovascular control has been implicated in triggering the ventricular arrhythmias.
J. Brugada, J. Montserrat, E. Tobaldini, P. Leinveber, P. G. Macedo, V. K. Somers, I. Molina, B. Benito, N. Montano, T. Kara, A. Porta   +10 more
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Brugada Syndrome in Japan

Circulation Journal, 2007
The incidence of Brugada syndrome (BS) is relatively high in Japan compared with the rest of the world, ranging between 0.1% and 0.2% in the general population. BS in Japan, as in other countries, is most prevalent in middle-aged men, and has characteristics ECG changes, a high recurrence rate in symptomatic patients, and relatively low incidence of ...
openaire   +3 more sources

Detección de un síndrome de Brugada en un reconocimiento médico laboral Detection of a Brugada syndrome in a occupational medical examination

Medicina y Seguridad del Trabajo, 2011
El síndrome de Brugada es una cardiopatía genética y no estructural debida a una alteración primaria de los canales iónicos del miocardio y que se asocia a un riesgo de muerte súbita.
María Isabel Ruiz, Eva Marín, Santiago Nogüe, Pere Sanz-Gallén, Paola Berne, Lluis Mont, Josep Brugada   +6 more
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Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome

, 2006
BACKGROUND - Loss-of-function mutations in SCN5A have been associated with the Brugada syndrome. We report the first Brugada syndrome family with compound heterozygous mutations in SCN5A.
Hong, K., Antzelevitch, C., Pfeiffer, R., Hu, D., Brugada, J., Dumaine, R., Cordeiro, J.M., Orsino, A.-M., Brugada, P., Brugada, R., Barajas-Martinez, H., Wu, Y.S., Burashnikov, E.   +12 more
core   +1 more source