145 related articles for article (PubMed ID: 34999275)
1. Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing.
Novelli V; Memmi M; Malovini A; Mazzanti A; Liu N; Yanfei R; Bongianino R; Denegri M; Monteforte N; Bloise R; Morini M; Napolitano C
Heart Rhythm; 2022 May; 19(5):798-806. PubMed ID: 34999275
[TBL] [Abstract][Full Text] [Related]
2. Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Béziau DM; Barc J; O'Hara T; Le Gloan L; Amarouch MY; Solnon A; Pavin D; Lecointe S; Bouillet P; Gourraud JB; Guicheney P; Denjoy I; Redon R; Mabo P; le Marec H; Loussouarn G; Kyndt F; Schott JJ; Probst V; Baró I
Basic Res Cardiol; 2014; 109(6):446. PubMed ID: 25341504
[TBL] [Abstract][Full Text] [Related]
3. Gain-of-function KCNH2 mutations in patients with Brugada syndrome.
Wang QI; Ohno S; Ding WG; Fukuyama M; Miyamoto A; Itoh H; Makiyama T; Wu J; Bai J; Hasegawa K; Shinohara T; Takahashi N; Shimizu A; Matsuura H; Horie M
J Cardiovasc Electrophysiol; 2014 May; 25(5):522-530. PubMed ID: 24400717
[TBL] [Abstract][Full Text] [Related]
4. High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
Hasdemir C; Payzin S; Kocabas U; Sahin H; Yildirim N; Alp A; Aydin M; Pfeiffer R; Burashnikov E; Wu Y; Antzelevitch C
Heart Rhythm; 2015 Jul; 12(7):1584-94. PubMed ID: 25998140
[TBL] [Abstract][Full Text] [Related]
5. Novel SCN10A variants associated with Brugada syndrome.
Fukuyama M; Ohno S; Makiyama T; Horie M
Europace; 2016 Jun; 18(6):905-11. PubMed ID: 25842276
[TBL] [Abstract][Full Text] [Related]
6. Genotype-Phenotype Correlation of
Milman A; Behr ER; Gray B; Johnson DC; Andorin A; Hochstadt A; Gourraud JB; Maeda S; Takahashi Y; Jm Juang J; Kim SH; Kamakura T; Aiba T; Postema PG; Mizusawa Y; Denjoy I; Giustetto C; Conte G; Huang Z; Sarquella-Brugada G; Mazzanti A; Jespersen CH; Arbelo E; Brugada R; Calo L; Corrado D; Casado-Arroyo R; Allocca G; Takagi M; Delise P; Brugada J; Tfelt-Hansen J; Priori SG; Veltmann C; Yan GX; Brugada P; Gaita F; Leenhardt A; Wilde AAM; Kusano KF; Nam GB; Hirao K; Probst V; Belhassen B
Circ Genom Precis Med; 2021 Oct; 14(5):e003222. PubMed ID: 34461752
[TBL] [Abstract][Full Text] [Related]
7. Genetic Testing in Brugada Syndrome: A 30-Year Experience.
Pannone L; Bisignani A; Osei R; Gauthey A; Sorgente A; Monaco C; Della Rocca DG; Del Monte A; Strazdas A; Mojica J; Al Housari M; Miraglia V; Mouram S; Vetta G; Paparella G; Ramak R; Overeinder I; Bala G; Almorad A; Ströker E; Pappaert G; Sieira J; de Ravel T; La Meir M; Sarkozy A; Brugada P; Chierchia GB; Van Dooren S; de Asmundis C
Circ Arrhythm Electrophysiol; 2024 Apr; 17(4):e012374. PubMed ID: 38426305
[TBL] [Abstract][Full Text] [Related]
8. Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants.
Gray B; Hasdemir C; Ingles J; Aiba T; Makita N; Probst V; Wilde AAM; Newbury-Ecob R; Sheppard MN; Semsarian C; Sy RW; Behr ER
Heart Rhythm; 2018 Jul; 15(7):1051-1057. PubMed ID: 29758173
[TBL] [Abstract][Full Text] [Related]
9. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Makarawate P; Glinge C; Khongphatthanayothin A; Walsh R; Mauleekoonphairoj J; Amnueypol M; Prechawat S; Wongcharoen W; Krittayaphong R; Anannab A; Lichtner P; Meitinger T; Tjong FVY; Lieve KVV; Amin AS; Sahasatas D; Ngarmukos T; Wichadakul D; Payungporn S; Sutjaporn B; Wandee P; Poovorawan Y; Tfelt-Hansen J; Tanck MWT; Tadros R; Wilde AAM; Bezzina CR; Veerakul G; Nademanee K
Heart Rhythm; 2020 Dec; 17(12):2145-2153. PubMed ID: 32619740
[TBL] [Abstract][Full Text] [Related]
10. In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
Pham HM; Nguyen DP; Ta TD; Le TP; Phan PH; Trinh HA; Tran TV; Luong TLA; Nguyen HM; Bui TH; Tran TH; Ta TV; Tran VK
Mol Genet Genomic Med; 2023 Dec; 11(12):e2263. PubMed ID: 37547970
[TBL] [Abstract][Full Text] [Related]
11. High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.
Risgaard B; Jabbari R; Refsgaard L; Holst AG; Haunsø S; Sadjadieh A; Winkel BG; Olesen MS; Tfelt-Hansen J
Clin Genet; 2013 Nov; 84(5):489-95. PubMed ID: 23414114
[TBL] [Abstract][Full Text] [Related]
12.
Wijeyeratne YD; Tanck MW; Mizusawa Y; Batchvarov V; Barc J; Crotti L; Bos JM; Tester DJ; Muir A; Veltmann C; Ohno S; Page SP; Galvin J; Tadros R; Muggenthaler M; Raju H; Denjoy I; Schott JJ; Gourraud JB; Skoric-Milosavljevic D; Nannenberg EA; Redon R; Papadakis M; Kyndt F; Dagradi F; Castelletti S; Torchio M; Meitinger T; Lichtner P; Ishikawa T; Wilde AAM; Takahashi K; Sharma S; Roden DM; Borggrefe MM; McKeown PP; Shimizu W; Horie M; Makita N; Aiba T; Ackerman MJ; Schwartz PJ; Probst V; Bezzina CR; Behr ER
Circ Genom Precis Med; 2020 Dec; 13(6):e002911. PubMed ID: 33164571
[TBL] [Abstract][Full Text] [Related]
13. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
Rudic B; Schimpf R; Veltmann C; Doesch C; Tülümen E; Schoenberg SO; Borggrefe M; Papavassiliu T
Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399
[TBL] [Abstract][Full Text] [Related]
14. Systematic re-evaluation of SCN5A variants associated with Brugada syndrome.
Denham NC; Pearman CM; Ding WY; Waktare J; Gupta D; Snowdon R; Hall M; Cooper R; Modi S; Todd D; Mahida S
J Cardiovasc Electrophysiol; 2019 Jan; 30(1):118-127. PubMed ID: 30203441
[TBL] [Abstract][Full Text] [Related]
15. Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?
Daimi H; Khelil AH; Neji A; Ben Hamda K; Maaoui S; Aranega A; Be Chibani J; Franco D
Biomed J; 2019 Aug; 42(4):252-260. PubMed ID: 31627867
[TBL] [Abstract][Full Text] [Related]
16. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Kapplinger JD; Tester DJ; Alders M; Benito B; Berthet M; Brugada J; Brugada P; Fressart V; Guerchicoff A; Harris-Kerr C; Kamakura S; Kyndt F; Koopmann TT; Miyamoto Y; Pfeiffer R; Pollevick GD; Probst V; Zumhagen S; Vatta M; Towbin JA; Shimizu W; Schulze-Bahr E; Antzelevitch C; Salisbury BA; Guicheney P; Wilde AA; Brugada R; Schott JJ; Ackerman MJ
Heart Rhythm; 2010 Jan; 7(1):33-46. PubMed ID: 20129283
[TBL] [Abstract][Full Text] [Related]
17. Functional Characterization of Two Novel Mutations in
Balla C; Conte E; Selvatici R; Marsano RM; Gerbino A; Farnè M; Blunck R; Vitali F; Armaroli A; Brieda A; Liantonio A; De Luca A; Ferlini A; Rapezzi C; Bertini M; Gualandi F; Imbrici P
Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34204499
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Burashnikov E; Pfeiffer R; Barajas-Martinez H; Delpón E; Hu D; Desai M; Borggrefe M; Häissaguerre M; Kanter R; Pollevick GD; Guerchicoff A; Laiño R; Marieb M; Nademanee K; Nam GB; Robles R; Schimpf R; Stapleton DD; Viskin S; Winters S; Wolpert C; Zimmern S; Veltmann C; Antzelevitch C
Heart Rhythm; 2010 Dec; 7(12):1872-82. PubMed ID: 20817017
[TBL] [Abstract][Full Text] [Related]
19. Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy.
Curcio A; Malovini A; Mazzanti A; Memmi M; Gambelli P; La Rosa F; Bloise R; Indolfi C; Bellazzi R; Napolitano C
Heart Rhythm; 2021 Oct; 18(10):1698-1706. PubMed ID: 34245912
[TBL] [Abstract][Full Text] [Related]
20. Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.
Campuzano O; Sarquella-Brugada G; Fernandez-Falgueras A; Cesar S; Coll M; Mates J; Arbelo E; Perez-Serra A; Del Olmo B; Jordá P; Fiol V; Iglesias A; Puigmulé M; Lopez L; Pico F; Brugada J; Brugada R
Hum Mutat; 2019 Jun; 40(6):749-764. PubMed ID: 30821013
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]