Results 91 to 100 of about 17,670 (140)

The management of Brugada syndrome patients [PDF]

, 2006
Brugada syndrome is a congenital electrical disorder characterised by the appearance of distinctive QRST-T patterns in the right precordial leads and an increased risk of sudden death (SCD) in young healthy adults.
Ferreira, Sergio Dubner i Celso, Riera, Andrés Ricardo Pérez, Schapachnik, Edgardo, Uchida, Augusto Hiroshi, Zhang, Li   +4 more
core   +1 more source

New Insights Into the Genetic Basis of Inherited Arrhythmia Syndromes. [PDF]

, 2016
Behr, ER, Gray, B
core   +1 more source

Brugada Syndrome and Exercise: Is It Time for a Paradigm Change? [PDF]

J Cardiovasc Dev Dis
Gonçalves CM, Vazão A, Carvalho M, Cabral M, Martins A, Amado M, Pereira J, Saraiva F, Martins H, Dores H.   +9 more
europepmc   +1 more source

Brugada syndrome update. [PDF]

Front Physiol
Xu T, Wang S, Wang J, Xing J.
europepmc   +1 more source

Artificial intelligence for Brugada syndrome diagnosis and gene variants interpretation. [PDF]

Am J Cardiovasc Dis
Sahebnasagh M, Farjoo MH.
europepmc   +1 more source

SCN5A variant type-dependent risk prediction in Brugada syndrome. [PDF]

Europace
Aizawa T, Makiyama T, Huang H, Imamura T, Fukuyama M, Sonoda K, Kato K, Hisamatsu T, Nakamura Y, Hoshino K, Ozawa J, Suzuki H, Yasuda K, Aoki H, Kurita T, Yoshida Y, Suzuki T, Nakamura Y, Ogawa Y, Yamagami S, Morita H, Yuasa S, Fukuda M, Ono M, Kondo H, Takahashi N, Ohno S, Nakagawa Y, Ono K, Horie M.   +29 more
europepmc   +1 more source

Epicardial Ablation for Arrhythmogenic Disorders in Patients with Brugada Syndrome. [PDF]

Biomedicines
Matteucci A, Mariani MV, Sgarra L, Bonanni M, Frazzetto M, La Fazia VM, Pierucci N, Lavalle C, Pandozi C, Nardi F, Colivicchi F.   +10 more
europepmc   +1 more source

A Vision Transformer Model for the Prediction of Fatal Arrhythmic Events in Patients with Brugada Syndrome. [PDF]

Sensors (Basel)
Randazzo V, Caligari S, Pasero E, Giustetto C, Saglietto A, Bertarello W, Averbuch A, Marcus-Kalish M, Zheludev V, Gaita F.   +9 more
europepmc   +1 more source

The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome. [PDF]

Front Med (Lausanne), 2023
Greiner AM, Mehdi H, Cevan C, Gutmann R, London B.   +4 more
europepmc   +1 more source

NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implications. [PDF]

Eur Heart J
Tarantino A, Ciconte G, Melgari D, Frosio A, Ghiroldi A, Piccoli M, Villa M, Creo P, Calamaio S, Castoldi V, Coviello S, Micaglio E, Cirillo F, Locati ET, Negro G, Boccellino A, Mastrocinque F, Ćalović Ž, Ricagno S, Leocani L, Vicedomini G, Santinelli V, Rivolta I, Anastasia L, Pappone C.   +24 more
europepmc   +1 more source