Brugada syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Brugada syndrome" in English language version.

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68nih.gov

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Kohli U, Ravishankar C, Nordli D (December 2020). "Cardiac phenotypic spectrum of KCNT1 mutations". Cardiology in the Young. 30 (12): 1935–1939. doi:10.1017/S1047951120002735. ISSN 1047-9511. PMID 32883383. S2CID 221497594.

doi.org

Polovina MM, Vukicevic M, Banko B, Lip GY, Potpara TS (October 2017). "Brugada syndrome: A general cardiologist's perspective". European Journal of Internal Medicine. 44: 19–27. doi:10.1016/j.ejim.2017.06.019. PMID 28645806.
Sarquella-Brugada G, Campuzano O, Arbelo E, Brugada J, Brugada R (January 2016). "Brugada syndrome: clinical and genetic findings". Genetics in Medicine. 18 (1): 3–12. doi:10.1038/gim.2015.35. PMID 25905440.
Antzelevitch C, Patocskai B (January 2016). "Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects". Current Problems in Cardiology. 41 (1): 7–57. doi:10.1016/j.cpcardiol.2015.06.002. PMC 4737702. PMID 26671757.
Doty B, Kim E, Phelps J, Akpunonu P (8 July 2020). "Pathophysiology of Hyperkalemia Presenting as Brugada Pattern on Electrocardiogram (ECG)". The American Journal of Case Reports. 21: e923464. doi:10.12659/AJCR.923464. ISSN 1941-5923. PMC 7370581. PMID 32636355.
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. (December 2013). "HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013". Heart Rhythm. 10 (12): 1932–63. doi:10.1016/j.hrthm.2013.05.014. PMID 24011539.
Belhassen B, Glick A, Viskin S (September 2004). "Efficacy of quinidine in high-risk patients with Brugada syndrome". Circulation. 110 (13): 1731–7. doi:10.1161/01.CIR.0000143159.30585.90. PMID 15381640.
Martini B, Nava A, Thiene G, Buja GF, Canciani B, Scognamiglio R, Daliento L, Dalla Volta S (December 1989). "Ventricular fibrillation without apparent heart disease: description of six cases". American Heart Journal. 118 (6): 1203–9. doi:10.1016/0002-8703(89)90011-2. PMID 2589161. S2CID 24418607.
Brugada P, Brugada J (November 1992). "Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report". Journal of the American College of Cardiology. 20 (6): 1391–6. doi:10.1016/0735-1097(92)90253-J. PMID 1309182.
Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q (March 1998). "Genetic basis and molecular mechanism for idiopathic ventricular fibrillation". Nature. 392 (6673): 293–6. Bibcode:1998Natur.392..293C. doi:10.1038/32675. PMID 9521325. S2CID 4315426.
Postema PG, Wolpert C, Amin AS, Probst V, Borggrefe M, Roden DM, Priori SG, Tan HL, Hiraoka M, Brugada J, Wilde AA (September 2009). "Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)". Heart Rhythm. 6 (9): 1335–41. doi:10.1016/j.hrthm.2009.07.002. PMC 2779019. PMID 19716089.
Kapplinger JD, Tester DJ, Alders M, Benito B, Berthet M, Brugada J, et al. (January 2010). "An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing". Heart Rhythm. 7 (1): 33–46. doi:10.1016/j.hrthm.2009.09.069. PMC 2822446. PMID 20129283.
Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M (September 2009). "The genetic basis of Brugada syndrome: a mutation update". Human Mutation. 30 (9): 1256–66. doi:10.1002/humu.21066. PMID 19606473.
Ciconte G, Monasky MM, Santinelli V, Micaglio E, Vicedomini G, Anastasia L, Negro G, Borrelli V, Giannelli L, Santini F, de Innocentiis C, Rondine R, Locati ET, Bernardini A, Mazza BC, Mecarocci V, Ćalović Ž, Ghiroldi A, D'Imperio S, Benedetti S, Di Resta C, Rivolta I, Casari G, Petretto E, Pappone C (2021). "Brugada syndrome genetics is associated with phenotype severity". Eur Heart J. 42 (11): 1082–1090. doi:10.1093/eurheartj/ehaa942. PMC 7955973. PMID 33221895.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Pappone C, Ciconte G, Micaglio E, Monasky MM (2021). "Common modulators of Brugada syndrome phenotype do not affect SCN5A prognostic value". Eur Heart J. 42 (13): 1273–1274. doi:10.1093/eurheartj/ehab071. PMC 8014514. PMID 33595071.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Postema PG, Walsh R, Bezzina CR (2021). "Illuminating the path from genetics to clinical outcome in Brugada syndrome". Eur Heart J. 42 (11): 1091–1093. doi:10.1093/eurheartj/ehaa994. PMC 7955964. PMID 33444429.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Antzelevitch C (June 2007). "Genetic basis of Brugada syndrome". Heart Rhythm. 4 (6): 756–7. doi:10.1016/j.hrthm.2007.03.015. PMC 1989771. PMID 17556198.
Belbachir N, Portero V, Al Sayed ZR, Gourraud JB, Dilasser F, Jesel L, Guo H, Wu H, Gaborit N, Guilluy C, Girardeau A, Bonnaud S, Simonet F, Karakachoff M, Pattier S, Scott C, Burel S, Marionneau C, Chariau C, Gaignerie A, David L, Genin E, Deleuze JF, Dina C, Sauzeau V, Loirand G, Baró I, Schott JJ, Probst V, Wu JC, Redon R, Charpentier F, Le Scouarnec S (21 May 2019). "RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome". European Heart Journal. 40 (37): 3081–3094. doi:10.1093/eurheartj/ehz308. PMC 6769825. PMID 31114854.
Garcia-Elias A, Benito B (February 2018). "Ion Channel Disorders and Sudden Cardiac Death". International Journal of Molecular Sciences. 19 (3): 692. doi:10.3390/ijms19030692. PMC 5877553. PMID 29495624.
Hu D, Barajas-Martínez H, Pfeiffer R, Dezi F, Pfeiffer J, Buch T, Betzenhauser MJ, Belardinelli L, Kahlig KM, Rajamani S, DeAntonio HJ, Myerburg RJ, Ito H, Deshmukh P, Marieb M, Nam GB, Bhatia A, Hasdemir C, Haïssaguerre M, Veltmann C, Schimpf R, Borggrefe M, Viskin S, Antzelevitch C (July 2014). "Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome". Journal of the American College of Cardiology. 64 (1): 66–79. doi:10.1016/j.jacc.2014.04.032. PMC 4116276. PMID 24998131.
Monasky MM, Micaglio E, Vicedomini G, Locati ET, Ciconte G, Giannelli L, Giordano F, Crisà S, Vecchi M, Borrelli V, Ghiroldi A, D'Imperio S, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C (2019). "Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants". Europace. 21 (10): 1550–1558. doi:10.1093/europace/euz186. PMID 31292628. Retrieved 27 April 2021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Monasky MM, Micaglio E, Ciconte G, Pappone C (2020). "Brugada Syndrome: Oligogenic or Mendelian Disease?". Int J Mol Sci. 21 (5): 1687. doi:10.3390/ijms21051687. PMC 7084676. PMID 32121523.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Hoogendijk MG (2012). "Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathy". Frontiers in Physiology. 3: 144. doi:10.3389/fphys.2012.00144. PMC 3358709. PMID 22654761.
Kohli U, Ravishankar C, Nordli D (December 2020). "Cardiac phenotypic spectrum of KCNT1 mutations". Cardiology in the Young. 30 (12): 1935–1939. doi:10.1017/S1047951120002735. ISSN 1047-9511. PMID 32883383. S2CID 221497594.
Hasdemir C, Payzin S, Kocabas U, Sahin H, Yildirim N, Alp A, Aydin M, Pfeiffer R, Burashnikov E, Wu Y, Antzelevitch C (July 2015). "High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia". Heart Rhythm. 12 (7): 1584–94. doi:10.1016/j.hrthm.2015.03.015. PMID 25998140.
Letsas KP, Korantzopoulos P, Efremidis M, Weber R, Lioni L, Bakosis G, Vassilikos VP, Deftereos S, Sideris A, Arentz T (March 2013). "Sinus node disease in subjects with type 1 ECG pattern of Brugada syndrome". Journal of Cardiology. 61 (3): 227–31. doi:10.1016/j.jjcc.2012.12.006. PMID 23403368.
Wilde AA, Postema PG, Di Diego JM, Viskin S, Morita H, Fish JM, Antzelevitch C (October 2010). "The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarization". Journal of Molecular and Cellular Cardiology. 49 (4): 543–53. doi:10.1016/j.yjmcc.2010.07.012. PMC 2932806. PMID 20659475.
Obeyesekere MN, Klein GJ, Modi S, Leong-Sit P, Gula LJ, Yee R, Skanes AC, Krahn AD (December 2011). "How to perform and interpret provocative testing for the diagnosis of Brugada syndrome, long-QT syndrome, and catecholaminergic polymorphic ventricular tachycardia". Circulation: Arrhythmia and Electrophysiology. 4 (6): 958–64. doi:10.1161/CIRCEP.111.965947. PMID 22203660.
Wilde Aa, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG (November 2002). "Proposed diagnostic criteria for the Brugada syndrome". European Heart Journal. 23 (21): 1648–1654. doi:10.1053/euhj.2002.3382. ISSN 0195-668X. PMID 12448445.
Bayés de Luna A, Brugada J, Baranchuk A, Borggrefe M, Breithardt G, Goldwasser D, Lambiase P, Riera AP, Garcia-Niebla J, Pastore C, Oreto G (September 2012). "Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report". Journal of Electrocardiology. 45 (5): 433–442. doi:10.1016/j.jelectrocard.2012.06.004. ISSN 1532-8430. PMID 22920782.
Wolpert C, Echternach C, Veltmann C, Antzelevitch C, Thomas GP, Spehl S, Streitner F, Kuschyk J, Schimpf R, Haase KK, Borggrefe M (March 2005). "Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome". Heart Rhythm. 2 (3): 254–60. doi:10.1016/j.hrthm.2004.11.025. PMC 1474213. PMID 15851314.
Giudicessi JR, Ackerman MJ (January 2013). "Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise". Current Opinion in Cardiology. 28 (1): 63–71. doi:10.1097/HCO.0b013e32835b0a41. PMC 3705648. PMID 23128497.
Sroubek J, Probst V, Mazzanti A, Delise P, Hevia JC, Ohkubo K, et al. (February 2016). "Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis". Circulation. 133 (7): 622–30. doi:10.1161/CIRCULATIONAHA.115.017885. PMC 4758872. PMID 26797467.
Kubala M, Aïssou L, Traullé S, Gugenheim AL, Hermida JS (June 2012). "Use of implantable loop recorders in patients with Brugada syndrome and suspected risk of ventricular arrhythmia". Europace. 14 (6): 898–902. doi:10.1093/europace/eur319. PMID 21979995.
Gourraud JB, Barc J, Thollet A, Le Scouarnec S, Le Marec H, Schott JJ, Redon R, Probst V (2016). "The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance". Frontiers in Cardiovascular Medicine. 3: 9. doi:10.3389/fcvm.2016.00009. PMC 4842929. PMID 27200363.
Mascia G, Arbelo E, Ojeda JH, Solimene F, Brugada R, Brugada J (July 2017). "Brugada Syndrome and Exercise Practice: Current Knowledge, Shortcomings and Open Questions". International Journal of Sports Medicine. 38 (8): 573–581. doi:10.1055/s-0043-107240. PMID 28625016. S2CID 3868956.
Masrur S, Memon S, Thompson PD (May 2015). "Brugada syndrome, exercise, and exercise testing". Clinical Cardiology. 38 (5): 323–6. doi:10.1002/clc.22386. PMC 6711014. PMID 25955277.
Rickard J, Wilkoff BL (2016). "Advances in implantable cardioverter defibrillator therapy". Expert Review of Cardiovascular Therapy. 14 (3): 291–9. doi:10.1586/14779072.2016.1131124. PMID 26653411. S2CID 6423194.
Olde Nordkamp LR, Postema PG, Knops RE, van Dijk N, Limpens J, Wilde AA, de Groot JR (February 2016). "Implantable cardioverter-defibrillator harm in young patients with inherited arrhythmia syndromes: A systematic review and meta-analysis of inappropriate shocks and complications". Heart Rhythm. 13 (2): 443–54. doi:10.1016/j.hrthm.2015.09.010. PMID 26385533.
Yang F, Hanon S, Lam P, Schweitzer P (April 2009). "Quinidine revisited". The American Journal of Medicine. 122 (4): 317–21. doi:10.1016/j.amjmed.2008.11.019. PMID 19249010.
Kautzner J, Peichl P (June 2017). "Catheter ablation to prevent sudden cardiac death". International Journal of Cardiology. 237: 29–33. doi:10.1016/j.ijcard.2017.03.135. PMID 28433554.
Behere SP, Weindling SN (September 2017). "Brugada syndrome in children – Stepping into unchartered territory". Annals of Pediatric Cardiology. 10 (3): 248–258. doi:10.4103/apc.APC_49_17. PMC 5594936. PMID 28928611.
Brugada J, Brugada P, Brugada R (July 1999). "The syndrome of right bundle branch block ST segment elevation in V1 to V3 and sudden death--the Brugada syndrome". Europace. 1 (3): 156–66. doi:10.1053/eupc.1999.0033. PMID 11225790.
Nakajima K, Takeichi S, Nakajima Y, Fujita MQ (April 2011). "Pokkuri Death Syndrome; sudden cardiac death cases without coronary atherosclerosis in South Asian young males". Forensic Science International. 207 (1–3): 6–13. doi:10.1016/j.forsciint.2010.10.018. PMID 21084168.
Nademanee K, Veerakul G, Nimmannit S, Chaowakul V, Bhuripanyo K, Likittanasombat K, Tunsanga K, Kuasirikul S, Malasit P, Tansupasawadikul S, Tatsanavivat P (October 1997). "Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men". Circulation. 96 (8): 2595–600. doi:10.1161/01.CIR.96.8.2595. PMID 9355899.
Mizusawa Y, Wilde AA (June 2012). "Brugada syndrome". Circulation: Arrhythmia and Electrophysiology. 5 (3): 606–16. doi:10.1161/CIRCEP.111.964577. PMID 22715240.
Brugada P (March 2016). "Brugada syndrome: More than 20 years of scientific excitement". Journal of Cardiology. 67 (3): 215–20. doi:10.1016/j.jjcc.2015.08.009. PMID 26627541.

ghostarchive.org

"Unsolved Mysteries with Robert Stack - Season 4, Episode 24 - Full Episode - YouTube". www.youtube.com. 8 March 2019. Archived from the original on 11 December 2021.

harvard.edu

ui.adsabs.harvard.edu

Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q (March 1998). "Genetic basis and molecular mechanism for idiopathic ventricular fibrillation". Nature. 392 (6673): 293–6. Bibcode:1998Natur.392..293C. doi:10.1038/32675. PMID 9521325. S2CID 4315426.

nih.gov

pubmed.ncbi.nlm.nih.gov

Polovina MM, Vukicevic M, Banko B, Lip GY, Potpara TS (October 2017). "Brugada syndrome: A general cardiologist's perspective". European Journal of Internal Medicine. 44: 19–27. doi:10.1016/j.ejim.2017.06.019. PMID 28645806.
Sarquella-Brugada G, Campuzano O, Arbelo E, Brugada J, Brugada R (January 2016). "Brugada syndrome: clinical and genetic findings". Genetics in Medicine. 18 (1): 3–12. doi:10.1038/gim.2015.35. PMID 25905440.
Antzelevitch C, Patocskai B (January 2016). "Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects". Current Problems in Cardiology. 41 (1): 7–57. doi:10.1016/j.cpcardiol.2015.06.002. PMC 4737702. PMID 26671757.
Doty B, Kim E, Phelps J, Akpunonu P (8 July 2020). "Pathophysiology of Hyperkalemia Presenting as Brugada Pattern on Electrocardiogram (ECG)". The American Journal of Case Reports. 21: e923464. doi:10.12659/AJCR.923464. ISSN 1941-5923. PMC 7370581. PMID 32636355.
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. (December 2013). "HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013". Heart Rhythm. 10 (12): 1932–63. doi:10.1016/j.hrthm.2013.05.014. PMID 24011539.
Belhassen B, Glick A, Viskin S (September 2004). "Efficacy of quinidine in high-risk patients with Brugada syndrome". Circulation. 110 (13): 1731–7. doi:10.1161/01.CIR.0000143159.30585.90. PMID 15381640.
Martini B, Nava A, Thiene G, Buja GF, Canciani B, Scognamiglio R, Daliento L, Dalla Volta S (December 1989). "Ventricular fibrillation without apparent heart disease: description of six cases". American Heart Journal. 118 (6): 1203–9. doi:10.1016/0002-8703(89)90011-2. PMID 2589161. S2CID 24418607.
Brugada P, Brugada J (November 1992). "Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report". Journal of the American College of Cardiology. 20 (6): 1391–6. doi:10.1016/0735-1097(92)90253-J. PMID 1309182.
Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q (March 1998). "Genetic basis and molecular mechanism for idiopathic ventricular fibrillation". Nature. 392 (6673): 293–6. Bibcode:1998Natur.392..293C. doi:10.1038/32675. PMID 9521325. S2CID 4315426.
Postema PG, Wolpert C, Amin AS, Probst V, Borggrefe M, Roden DM, Priori SG, Tan HL, Hiraoka M, Brugada J, Wilde AA (September 2009). "Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)". Heart Rhythm. 6 (9): 1335–41. doi:10.1016/j.hrthm.2009.07.002. PMC 2779019. PMID 19716089.
Kapplinger JD, Tester DJ, Alders M, Benito B, Berthet M, Brugada J, et al. (January 2010). "An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing". Heart Rhythm. 7 (1): 33–46. doi:10.1016/j.hrthm.2009.09.069. PMC 2822446. PMID 20129283.
Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M (September 2009). "The genetic basis of Brugada syndrome: a mutation update". Human Mutation. 30 (9): 1256–66. doi:10.1002/humu.21066. PMID 19606473.
Ciconte G, Monasky MM, Santinelli V, Micaglio E, Vicedomini G, Anastasia L, Negro G, Borrelli V, Giannelli L, Santini F, de Innocentiis C, Rondine R, Locati ET, Bernardini A, Mazza BC, Mecarocci V, Ćalović Ž, Ghiroldi A, D'Imperio S, Benedetti S, Di Resta C, Rivolta I, Casari G, Petretto E, Pappone C (2021). "Brugada syndrome genetics is associated with phenotype severity". Eur Heart J. 42 (11): 1082–1090. doi:10.1093/eurheartj/ehaa942. PMC 7955973. PMID 33221895.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Pappone C, Ciconte G, Micaglio E, Monasky MM (2021). "Common modulators of Brugada syndrome phenotype do not affect SCN5A prognostic value". Eur Heart J. 42 (13): 1273–1274. doi:10.1093/eurheartj/ehab071. PMC 8014514. PMID 33595071.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Postema PG, Walsh R, Bezzina CR (2021). "Illuminating the path from genetics to clinical outcome in Brugada syndrome". Eur Heart J. 42 (11): 1091–1093. doi:10.1093/eurheartj/ehaa994. PMC 7955964. PMID 33444429.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Antzelevitch C (June 2007). "Genetic basis of Brugada syndrome". Heart Rhythm. 4 (6): 756–7. doi:10.1016/j.hrthm.2007.03.015. PMC 1989771. PMID 17556198.
Belbachir N, Portero V, Al Sayed ZR, Gourraud JB, Dilasser F, Jesel L, Guo H, Wu H, Gaborit N, Guilluy C, Girardeau A, Bonnaud S, Simonet F, Karakachoff M, Pattier S, Scott C, Burel S, Marionneau C, Chariau C, Gaignerie A, David L, Genin E, Deleuze JF, Dina C, Sauzeau V, Loirand G, Baró I, Schott JJ, Probst V, Wu JC, Redon R, Charpentier F, Le Scouarnec S (21 May 2019). "RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome". European Heart Journal. 40 (37): 3081–3094. doi:10.1093/eurheartj/ehz308. PMC 6769825. PMID 31114854.
Garcia-Elias A, Benito B (February 2018). "Ion Channel Disorders and Sudden Cardiac Death". International Journal of Molecular Sciences. 19 (3): 692. doi:10.3390/ijms19030692. PMC 5877553. PMID 29495624.
Hu D, Barajas-Martínez H, Pfeiffer R, Dezi F, Pfeiffer J, Buch T, Betzenhauser MJ, Belardinelli L, Kahlig KM, Rajamani S, DeAntonio HJ, Myerburg RJ, Ito H, Deshmukh P, Marieb M, Nam GB, Bhatia A, Hasdemir C, Haïssaguerre M, Veltmann C, Schimpf R, Borggrefe M, Viskin S, Antzelevitch C (July 2014). "Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome". Journal of the American College of Cardiology. 64 (1): 66–79. doi:10.1016/j.jacc.2014.04.032. PMC 4116276. PMID 24998131.
Monasky MM, Micaglio E, Vicedomini G, Locati ET, Ciconte G, Giannelli L, Giordano F, Crisà S, Vecchi M, Borrelli V, Ghiroldi A, D'Imperio S, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C (2019). "Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants". Europace. 21 (10): 1550–1558. doi:10.1093/europace/euz186. PMID 31292628. Retrieved 27 April 2021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Monasky MM, Micaglio E, Ciconte G, Pappone C (2020). "Brugada Syndrome: Oligogenic or Mendelian Disease?". Int J Mol Sci. 21 (5): 1687. doi:10.3390/ijms21051687. PMC 7084676. PMID 32121523.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Hoogendijk MG (2012). "Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathy". Frontiers in Physiology. 3: 144. doi:10.3389/fphys.2012.00144. PMC 3358709. PMID 22654761.
Kohli U, Ravishankar C, Nordli D (December 2020). "Cardiac phenotypic spectrum of KCNT1 mutations". Cardiology in the Young. 30 (12): 1935–1939. doi:10.1017/S1047951120002735. ISSN 1047-9511. PMID 32883383. S2CID 221497594.
Hasdemir C, Payzin S, Kocabas U, Sahin H, Yildirim N, Alp A, Aydin M, Pfeiffer R, Burashnikov E, Wu Y, Antzelevitch C (July 2015). "High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia". Heart Rhythm. 12 (7): 1584–94. doi:10.1016/j.hrthm.2015.03.015. PMID 25998140.
Letsas KP, Korantzopoulos P, Efremidis M, Weber R, Lioni L, Bakosis G, Vassilikos VP, Deftereos S, Sideris A, Arentz T (March 2013). "Sinus node disease in subjects with type 1 ECG pattern of Brugada syndrome". Journal of Cardiology. 61 (3): 227–31. doi:10.1016/j.jjcc.2012.12.006. PMID 23403368.
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Doty B, Kim E, Phelps J, Akpunonu P (8 July 2020). "Pathophysiology of Hyperkalemia Presenting as Brugada Pattern on Electrocardiogram (ECG)". The American Journal of Case Reports. 21: e923464. doi:10.12659/AJCR.923464. ISSN 1941-5923. PMC 7370581. PMID 32636355.
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Kohli U, Ravishankar C, Nordli D (December 2020). "Cardiac phenotypic spectrum of KCNT1 mutations". Cardiology in the Young. 30 (12): 1935–1939. doi:10.1017/S1047951120002735. ISSN 1047-9511. PMID 32883383. S2CID 221497594.
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