- Treating Brugada Syndrome: A Case of Successful Radiofrequency Catheter Ablation
- Unraveling an Uncommon Encounter: Hypokalemic Periodic Paralysis with Brugada Phenocopy Amidst Hypokalemia
- Brugada Phenocopy due to Hyponatremia: A Case Report and Review of the Literature
- Left internal thoracic artery injury in percutaneous epicardial access for catheter ablation: Prevention and management
- Manuscript Title: Brugada syndrome in sports cardiology: an expert opinion statement of the Italian society of sports cardiology (SICSport)
- Repolarization Mapping in Brugada Syndrome Patients: How to Deal With Monophasic Complexes?
- Reply: Repolarization Mapping in Brugada Syndrome Patients: How to Deal With Monophasic Complexes?
- Paroxysmal, Persistent, and Permanent Type-1 Brugada Pattern: Does Burden Matter?
- Effective discrimination of wide QRS complex tachycardia with a new algorithm - the Prelocalization Series Algorithm
- Irregular rhythm with wide-QRS complexes and repolarization abnormalities in the emergency department: A nightmare ECG
- Exploring locoregional anaesthesia in Brugada syndrome: Balancing risk with innovation
- Assessment of adverse events of the novel antiepileptic drug lamotrigine: a real-world pharmacovigilance study based on FAERS
- Hyperkalemia-induced Brugada phenocopy: a systematic review of case reports
- A Vision Transformer Model for the Prediction of Fatal Arrhythmic Events in Patients with Brugada Syndrome
- Eighteen-year analysis of anaesthetic management in Brugada syndrome: The BRUGANAES study
- Efficacy of low-dose quinidine in patients with symptomatic Brugada syndrome
- SCN5A variant type-dependent risk prediction in Brugada syndrome
- Sex-specific clinical course of young patients with Brugada syndrome
- Genetic background and clinical phenotype in a Vietnamese cohort with Brugada syndrome: A whole exome sequencing study
- Brugada syndrome update
- Asymptomatic Brugada syndrome: Navigating implantable cardioverter-defibrillator implantation dilemma
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Incidence of spontaneous Brugada ECG during follow-up in patients with drug-inducible pattern: a systematic review and meta-analysis
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome
- Clinical association of the SCN5A c.2302A>G variant (p.Ile768Val) with Brugada syndrome