187 related articles for article (PubMed ID: 35331424)
1. Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome.
Suzuki K; Sonoda K; Aoki H; Nakamura Y; Watanabe S; Yoshida Y; Hoshino K; Ozawa J; Imamura T; Aiba T; Kato K; Makiyama T; Kusano K; Horie M; Ohno S
JACC Clin Electrophysiol; 2022 Mar; 8(3):297-305. PubMed ID: 35331424
[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. 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]
4. 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]
5. Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.
Maury P; Moreau A; Hidden-Lucet F; Leenhardt A; Fressart V; Berthet M; Denjoy I; Bennamar N; Rollin A; Cardin C; Guicheney P; Chahine M
J Interv Card Electrophysiol; 2013 Aug; 37(2):131-40. PubMed ID: 23612926
[TBL] [Abstract][Full Text] [Related]
6. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
[TBL] [Abstract][Full Text] [Related]
7. Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations.
Ortiz-Bonnin B; Rinné S; Moss R; Streit AK; Scharf M; Richter K; Stöber A; Pfeufer A; Seemann G; Kääb S; Beckmann BM; Decher N
Pflugers Arch; 2016 Aug; 468(8):1375-87. PubMed ID: 27287068
[TBL] [Abstract][Full Text] [Related]
8. A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
Tan BY; Yong RY; Barajas-Martinez H; Dumaine R; Chew YX; Wasan PS; Ching CK; Ho KL; Gan LS; Morin N; Chong AP; Yap SH; Neo JL; Yap EP; Moochhala S; Chong DT; Chow W; Seow SC; Hu D; Uttamchandani M; Teo WS
Europace; 2016 Jun; 18(6):897-904. PubMed ID: 25829473
[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. 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]
11. 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]
12. GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome.
Semino F; Darche FF; Bruehl C; Koenen M; Skladny H; Katus HA; Frey N; Draguhn A; Schweizer PA
Pflugers Arch; 2024 Feb; 476(2):229-242. PubMed ID: 38036776
[TBL] [Abstract][Full Text] [Related]
13. Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
Veltmann C; Barajas-Martinez H; Wolpert C; Borggrefe M; Schimpf R; Pfeiffer R; Cáceres G; Burashnikov E; Antzelevitch C; Hu D
J Am Heart Assoc; 2016 Jul; 5(7):. PubMed ID: 27381756
[TBL] [Abstract][Full Text] [Related]
14. Functional Analysis of SCN5A Genetic Variants Associated with Brugada Syndrome.
Mikhailova VB; Karpushev AV; Vavilova VD; Klimenko ES; Tulintseva T; Yudina YS; Vasichkina ES; Zhorov BS; Kostareva A
Cardiology; 2022; 147(1):35-46. PubMed ID: 34628415
[TBL] [Abstract][Full Text] [Related]
15. Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan.
Juang JM; Tsai CT; Lin LY; Liu YB; Yu CC; Hwang JJ; Chen JJ; Chiu FC; Chen WJ; Tseng CD; Chiang FT; Yeh HM; Sherri Yeh SF; Lai LP; Lin JL
J Formos Med Assoc; 2015 Jul; 114(7):620-6. PubMed ID: 26154754
[TBL] [Abstract][Full Text] [Related]
16.
Makarawate P; Chaosuwannakit N; Vannaprasaht S; Sahasthas D; Koo SH; Lee EJD; Tassaneeyakul W; Barajas-Martinez H; Hu D; Sawanyawisuth K
J Am Heart Assoc; 2017 Jun; 6(6):. PubMed ID: 28584071
[TBL] [Abstract][Full Text] [Related]
17. Relationship between sodium channel function and clinical phenotype in SCN5A variants associated with Brugada syndrome.
Pearman CM; Denham NC; Mills RW; Ding WY; Modi SS; Hall MCS; Todd DM; Mahida S
Hum Mutat; 2020 Dec; 41(12):2195-2204. PubMed ID: 33131149
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Distinct Features of Probands With Early Repolarization and Brugada Syndromes Carrying SCN5A Pathogenic Variants.
Zhang ZH; Barajas-Martínez H; Xia H; Li B; Capra JA; Clatot J; Chen GX; Chen X; Yang B; Jiang H; Tse G; Aizawa Y; Gollob MH; Scheinman M; Antzelevitch C; Hu D
J Am Coll Cardiol; 2021 Oct; 78(16):1603-1617. PubMed ID: 34649698
[TBL] [Abstract][Full Text] [Related]
20. SCN5A(K817E), a novel Brugada syndrome-associated mutation that alters the activation gating of NaV1.5 channel.
Kinoshita K; Takahashi H; Hata Y; Nishide K; Kato M; Fujita H; Yoshida S; Murai K; Mizumaki K; Nishida K; Yamaguchi Y; Kano M; Tabata T; Nishida N
Heart Rhythm; 2016 May; 13(5):1113-1120. PubMed ID: 26776555
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]