Results 51 to 60 of about 1,147,137 (221)

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

Indian 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, Md. Abdus Salam, Md. Zahirul Haque, A.K.M. Monwarul Islam   +3 more
doaj   +1 more source

Brugada phenocopy or congenital Brugada syndrome in a patient with spontaneous pneumopericardium and pericarditis

Journal of Arrhythmia, 2021
Brugada syndrome (BrS) is characterized by coved ST segment elevation in the right precordial lead (V1‐V3). Previous reports have described type‐1 or type‐2 Brugada ECG pattern as a Brugada phenocopy (BrP) in various clinical condition and once the ...
Pichmanil Khmao, Vannak Long, No Ku, Sivutha Lim   +3 more
doaj   +1 more source

Hyperkalemia-induced brugada phenocopy: A rare electrocardiogram manifestation

Journal of the Practice of Cardiovascular Sciences, 2022
Hyperkalemia-induced Brugada ECG pattern is rare. Although the association of hyperkalemia with Brugada pattern is a known entity, it is also very important to be aware of this presentation as the treatment of this Brugada Phenocopy is different from ...
Satyajit Singh, Chandra Prakash Thakur, Surendra Naik, Muneshwar Kumar   +3 more
doaj   +1 more source

Genetics of Brugada syndrome [PDF]

Journal of Human Genetics, 2015
The Brugada syndrome is characterized by unique 'coved-type' ST-segment elevation in the right precordial leads of electrocardiogram and ventricular fibrillation, and is responsible for 4 to 12% of sudden cardiac death in the general population. The frequency is higher in Southeast Asia including Japan compared with Western countries.
Hiroshi, Watanabe, Tohru, Minamino
openaire   +2 more sources

Late INa as a Therapeutic Target: New Strategies, Computational Modelling, Drug Development, and Clinical Translation

Medicinal Research Reviews, EarlyView.
ABSTRACT The Nav1.5 channel, a major isoform of voltage‐gated sodium ion channel, is mainly found in ventricular cardiomyocytes, playing a key role in generating essential cardiac action potentials for normal heart rhythms. Mutations in Nav1.5 have been associated with severe heart conditions such as long QT syndrome, Brugada syndrome, cardiac ...
Arkapravo Chattopadhyay, Lynn C. Lunsonga, Peter E. Light, Khaled Barakat   +3 more
wiley   +1 more source

Treatment of Electrical Storm with Amiodarone in Brugada Syndrome- an Unexpected Protective Effect [PDF]

, 2013
We are reporting on a 53 year old man with proven Brugada syndrome and ICD implantation for resuscitation in context of polymorphic VT. After recurrent arrhythmia he was treated with Amiodarone.
Novak, J, Lambiase, PD
core  

Brugada syndrome - Report of the second consensus conference

, 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.
Shimizu, Wataru, Perez Riera, Andres Ricardo, BRUGADA J, GUSSAK I, LeMarec, Herve, BORGGREFE M, SCHULZE BAHR E, TAN H, NADEMANEE K, Brugada, Josep, BRUGADA R, ANTZELEVITCH C, SHIMIZU W, BRUGADA P, Schulze-Bahr, Eric, Gussak, Ihor, Nademanee, Koonlawee, Wilde, Arthur, WILDE A., CORRADO, DOMENICO, Antzelevitch, Charles, Brugada, Ramon, LEMAREC H, Tan, Hanno, RIERA ARP, Brugada, Pedro, Borggrefe, Martin   +26 more
core   +1 more source

Brugada syndrome: 1992–2002 A historical perspective [PDF]

, 2003
An intriguing new clinical entity characterized by ST-segment elevation in the right precordial electrocardiographic leads and a high incidence of sudden death in individuals with structurally normal hearts was described by Pedro and Josep Brugada in ...
Pedro Brugada, Nademanee, Kolawanee, Kolawanee Nademanee, Josep Brugada, Antzelevitch, Charles, Brugada, Ramon, Charles Antzelevitch, Ramon Brugada, Jeffrey A Towbin, Brugada, Josep, Brugada, Pedro, Towbin, Jeffrey A   +11 more
core   +1 more source

Brugada Syndrome and GPD1L: Definite Genotype-Phenotype Association?

Cardiogenetics
The GPD1L gene encodes a small cytoplasmic protein that is involved in the regulation of sodium currents. Alterations in this gene have been associated with Brugada syndrome.
Andrea Greco, Estefanía Martínez-Barrios, José Cruzalegui, Sergi Cesar, Fredy Chipa, Nuria Díez-Escuté, Patricia Cerralbo, Irene Zschaeck, Paula Loredo, Georgia Sarquella-Brugada, Oscar Campuzano   +10 more
doaj   +1 more source

Forensic challenges in a case of suspected filicide, matricide, and post‐mortem dismemberment

Journal of Forensic Sciences, EarlyView.
Abstract Familicide represents one of the most complex forms of domestic violence in forensic practice. Among intrafamilial homicides, filicide and matricide pose major medico‐legal and criminological challenges, particularly when autopsy findings are nonspecific or severely altered by post‐mortem changes.
Isabella Caristo, Rosario Barranco, Giulio Fraternali Orcioni, Domenico Coviello, Francesco Ventura   +4 more
wiley   +1 more source