Aims The typical Brugada ECG pattern consists of a prominent J-wave associated with ST-segment elevation localized in the right precordial leads V1–V3. In many patients, the ECG presents periods of transient normalization and the Brugada-phenotype can be unmasked by the administration of class-I antiarrhythmics. Reports have documented the heterogeneity of the Brugada syndrome ECG-phenotype characterized by unusual localization of the ECG abnormalities in the inferior leads. Case report A 51-year-old man, without detectable structural heart disease, was referred to us because of a history of syncope, dizziness, and palpitations. The ECG showed a J-wave and ST-segment elevation in the right precordial leads, suggesting Brugada syndrome. As o...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
Microvolt 2:1 T wave alternans (TWA) and increased beat-to-beat repolarization variability have been...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
Aims: The typical Brugada ECG pattern consists of a prominent J-wave associated with ST-segment elev...
OBJECTIVE: ST-segment elevation in the right precordial electrocardiography (ECG) leads in Brugada s...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
Brugada syndrome is a hereditary arrhythmic disease characterized by the presence of coved ST elevat...
Objectives We sought to obtain new insights into the pathophysiologic basis of Brugada syndrome (BrS...
Brugada syndrome is a genetic disease characterized by persistent or transient ST elevation in the r...
International audienceAIMS: The diagnostic type I ECG in Brugada syndrome (BS) is often concealed an...
Brugada syndrome (BS) is associated with sudden cardiac death in patients with a structurally normal...
In 1992, Brugada syndrom was introduced as a new clinical entity linking typical but variable ST seg...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
A 31-year-old male patient presented with complaints of palpitations, dizziness, and recurrent episo...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
Microvolt 2:1 T wave alternans (TWA) and increased beat-to-beat repolarization variability have been...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
Aims: The typical Brugada ECG pattern consists of a prominent J-wave associated with ST-segment elev...
OBJECTIVE: ST-segment elevation in the right precordial electrocardiography (ECG) leads in Brugada s...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
Brugada syndrome is a hereditary arrhythmic disease characterized by the presence of coved ST elevat...
Objectives We sought to obtain new insights into the pathophysiologic basis of Brugada syndrome (BrS...
Brugada syndrome is a genetic disease characterized by persistent or transient ST elevation in the r...
International audienceAIMS: The diagnostic type I ECG in Brugada syndrome (BS) is often concealed an...
Brugada syndrome (BS) is associated with sudden cardiac death in patients with a structurally normal...
In 1992, Brugada syndrom was introduced as a new clinical entity linking typical but variable ST seg...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
A 31-year-old male patient presented with complaints of palpitations, dizziness, and recurrent episo...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
Microvolt 2:1 T wave alternans (TWA) and increased beat-to-beat repolarization variability have been...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...