349 related articles for article (PubMed ID: 24388542)
1. A second case with arrhythmogenic cardiomyopathy, provocable Brugada ECG and SCN5A mutation.
S P
Int J Cardiol; 2014 Feb; 171(3):e117-8. PubMed ID: 24388542
[No Abstract] [Full Text] [Related]
2. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
Wahbi K; Algalarrondo V; Bécane HM; Fressart V; Beldjord C; Azibi K; Lazarus A; Berber N; Radvanyi-Hoffman H; Stojkovic T; Béhin A; Laforêt P; Eymard B; Hatem S; Duboc D
Arch Cardiovasc Dis; 2013 Dec; 106(12):635-43. PubMed ID: 24140416
[TBL] [Abstract][Full Text] [Related]
3. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
Allegue C; Coll M; Mates J; Campuzano O; Iglesias A; Sobrino B; Brion M; Amigo J; Carracedo A; Brugada P; Brugada J; Brugada R
PLoS One; 2015; 10(7):e0133037. PubMed ID: 26230511
[TBL] [Abstract][Full Text] [Related]
4. [Genetic and molecular basis for sodium channel-mediated Brugada syndrome].
Barajas-Martínez H; Hu D; Antzelevitch C
Arch Cardiol Mex; 2013; 83(4):295-302. PubMed ID: 24269159
[TBL] [Abstract][Full Text] [Related]
5. Diagnosis of arrhythmogenic cardiomyopathy by localized right precordial QRS prolongation and inferior early repolarization phenomenon but without T-wave inversion.
Peters S
Int J Cardiol; 2016 Mar; 207():97-9. PubMed ID: 26797341
[No Abstract] [Full Text] [Related]
6. [SCN5A mutation in patients with Brugada electrocardiographic pattern induced by fever].
Yu JH; Hu JZ; Zhou H; Liu X; Cao Q; Shen Y; Ma JY; Zhou SZ; Liu XX; Li JX; Chen Q; Cheng XS; Hong K
Zhonghua Xin Xue Guan Bing Za Zhi; 2013 Dec; 41(12):1010-4. PubMed ID: 24524602
[TBL] [Abstract][Full Text] [Related]
7. Dual phenotypic transmission in Brugada syndrome.
Hermida JS; Arnalsteen-Dassonvalle E; Kubala M; Mathiron A; Traulle S; Anbazhagan K; Hermida A; Rochette J
Arch Cardiovasc Dis; 2013; 106(6-7):366-72. PubMed ID: 23810369
[TBL] [Abstract][Full Text] [Related]
8. [Cardiac sodium channelopathy from bench to bedside].
Zhang YM; Zhou N
Zhonghua Er Ke Za Zhi; 2013 Nov; 51(11):874-7. PubMed ID: 24484568
[No Abstract] [Full Text] [Related]
9. A novel mutation in the SCN5A gene contributes to arrhythmogenic characteristics of early repolarization syndrome.
Guo Q; Ren L; Chen X; Hou C; Chu J; Pu J; Zhang S
Int J Mol Med; 2016 Mar; 37(3):727-33. PubMed ID: 26820605
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. In Children and Adolescents From Brugada Syndrome-Families, Only
Peltenburg PJ; Blom NA; Vink AS; Kammeraad JAE; Breur HJMPJ; Rammeloo LAJ; Wilde AAM; Clur SB
Circulation; 2020 Jul; 142(1):89-91. PubMed ID: 32628552
[No Abstract] [Full Text] [Related]
13. Malignant response to ajmaline challenge in SCN5A mutation carriers: experience from a large familial study.
Gandjbakhch E; Fressart V; Duthoit G; Marquié C; Deharo JC; Pousset F; Hebert JL; Simon F; Himbert C; Klug D; Charron P; Hidden-Lucet F
Int J Cardiol; 2014 Mar; 172(1):256-8. PubMed ID: 24476701
[No Abstract] [Full Text] [Related]
14. Arrhythmogenic cardiomyopathy and provocable Brugada ECG in a patient caused by missense mutation in plakophilin-2.
Peters S
Int J Cardiol; 2014 May; 173(2):317-8. PubMed ID: 24681023
[No Abstract] [Full Text] [Related]
15. p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter.
Hothi SS; Ara F; Timperley J
J Cardiovasc Electrophysiol; 2015 Jan; 26(1):93-7. PubMed ID: 24903439
[TBL] [Abstract][Full Text] [Related]
16. Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy.
Wilde AAM; Amin AS
JACC Clin Electrophysiol; 2018 May; 4(5):569-579. PubMed ID: 29798782
[TBL] [Abstract][Full Text] [Related]
17. Low amplitude ECG and QRS fragmentation in provocable coved-type ST-segment elevation on surface ECG are strong predictors of a continuum between arrhythmogenic cardiomypathy and Brugada syndrome.
Peters S
Int J Cardiol; 2016 Jul; 214():148-50. PubMed ID: 27061648
[No Abstract] [Full Text] [Related]
18. An autopsy case of sudden unexpected nocturnal death syndrome with R1193Q polymorphism in the SCN5A gene.
Matsusue A; Kashiwagi M; Hara K; Waters B; Sugimura T; Kubo S
Leg Med (Tokyo); 2012 Nov; 14(6):317-9. PubMed ID: 22682427
[TBL] [Abstract][Full Text] [Related]
19. Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutation.
Hong K; Hu J; Yu J; Brugada R
Eur J Hum Genet; 2012 Nov; 20(11):1189-92. PubMed ID: 22490985
[TBL] [Abstract][Full Text] [Related]
20. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
Yagihara N; Watanabe H; Barnett P; Duboscq-Bidot L; Thomas AC; Yang P; Ohno S; Hasegawa K; Kuwano R; Chatel S; Redon R; Schott JJ; Probst V; Koopmann TT; Bezzina CR; Wilde AA; Nakano Y; Aiba T; Miyamoto Y; Kamakura S; Darbar D; Donahue BS; Shigemizu D; Tanaka T; Tsunoda T; Suda M; Sato A; Minamino T; Endo N; Shimizu W; Horie M; Roden DM; Makita N
J Am Heart Assoc; 2016 Sep; 5(9):. PubMed ID: 27625342
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
