Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar ECG findings predisposing individuals to ventricular arrhythmias, syncope, and sudden cardiac death (SCD). Various electrolyte disturbances and ion channels blocking drugs could also provoke BrS ECG findings without genetic BrS. Clinical differentiation and recognition are essential for guiding the legitimate action. Hyperkalemia is well known to cause a wide variety of ECG manifestations. Severe hyperkalemia can even cause life threatening ventricular arrhythmias and cardiac conduction abnormalities. Most common ECG findings include peaked tall T waves with short PR interval and wide QRS complex. Since it is very commonly encountered disorder,...
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and ca...
without ST elevation and no signs of Brugada. Considering this short period of time to normalisation...
Brugada syndrome (BS) is an inherited channelopathy associated with elevated risk of ventricular fib...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
Brugada syndrome was described in 1992 as a new clinical and electrocardiographic syndrome involving...
Brugada syndrome was described in 1992 as a new clinical and electrocardiographic syndrome involving...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
A 78-year-old man presented to the emergency department with a 10-day history of diarrhea and presyn...
Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmia...
Koomatie Ramsaroop,1 Rajeev Seecheran,1 Valmiki Seecheran,1 Sangeeta Persad,1 Stanley Giddings,2 Bor...
Background Several metabolic conditions can cause the Brugada ECG pattern, also called Brugada pheno...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Summary: Brugada syndrome (BS) is an arrhythmogenic ion channelopathy, which constitutes a distinct ...
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and ca...
without ST elevation and no signs of Brugada. Considering this short period of time to normalisation...
Brugada syndrome (BS) is an inherited channelopathy associated with elevated risk of ventricular fib...
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar EC...
Brugada syndrome was described in 1992 as a new clinical and electrocardiographic syndrome involving...
Brugada syndrome was described in 1992 as a new clinical and electrocardiographic syndrome involving...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
A 78-year-old man presented to the emergency department with a 10-day history of diarrhea and presyn...
Brugada syndrome is a heterogeneous genetic channelopathy that predisposes to ventricular arrhythmia...
Koomatie Ramsaroop,1 Rajeev Seecheran,1 Valmiki Seecheran,1 Sangeeta Persad,1 Stanley Giddings,2 Bor...
Background Several metabolic conditions can cause the Brugada ECG pattern, also called Brugada pheno...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Summary: Brugada syndrome (BS) is an arrhythmogenic ion channelopathy, which constitutes a distinct ...
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and ca...
without ST elevation and no signs of Brugada. Considering this short period of time to normalisation...
Brugada syndrome (BS) is an inherited channelopathy associated with elevated risk of ventricular fib...