260 related articles for article (PubMed ID: 25691538)
21. Functional characterization of SCN10A variants in several cases of sudden unexplained death.
Gando I; Williams N; Fishman GI; Sampson BA; Tang Y; Coetzee WA
Forensic Sci Int; 2019 Aug; 301():289-298. PubMed ID: 31195250
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases.
Hayashi K; Teramoto R; Nomura A; Asano Y; Beerens M; Kurata Y; Kobayashi I; Fujino N; Furusho H; Sakata K; Onoue K; Chiang DY; Kiviniemi TO; Buys E; Sips P; Burch ML; Zhao Y; Kelly AE; Namura M; Kita Y; Tsuchiya T; Kaku B; Oe K; Takeda Y; Konno T; Inoue M; Fujita T; Kato T; Funada A; Tada H; Hodatsu A; Nakanishi C; Sakamoto Y; Tsuda T; Nagata Y; Tanaka Y; Okada H; Usuda K; Cui S; Saito Y; MacRae CA; Takashima S; Yamagishi M; Kawashiri MA; Takamura M
Cardiovasc Res; 2020 Nov; 116(13):2116-2130. PubMed ID: 31977013
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26.
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]
27. Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
Nunn LM; Lopes LR; Syrris P; Murphy C; Plagnol V; Firman E; Dalageorgou C; Zorio E; Domingo D; Murday V; Findlay I; Duncan A; Carr-White G; Robert L; Bueser T; Langman C; Fynn SP; Goddard M; White A; Bundgaard H; Ferrero-Miliani L; Wheeldon N; Suvarna SK; O'Beirne A; Lowe MD; McKenna WJ; Elliott PM; Lambiase PD
Europace; 2016 Jun; 18(6):888-96. PubMed ID: 26498160
[TBL] [Abstract][Full Text] [Related]
28. Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
Selga E; Campuzano O; Pinsach-Abuin ML; Pérez-Serra A; Mademont-Soler I; Riuró H; Picó F; Coll M; Iglesias A; Pagans S; Sarquella-Brugada G; Berne P; Benito B; Brugada J; Porres JM; López Zea M; Castro-Urda V; Fernández-Lozano I; Brugada R
PLoS One; 2015; 10(7):e0132888. PubMed ID: 26173111
[TBL] [Abstract][Full Text] [Related]
29. Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.
Cerrone M; Lin X; Zhang M; Agullo-Pascual E; Pfenniger A; Chkourko Gusky H; Novelli V; Kim C; Tirasawadichai T; Judge DP; Rothenberg E; Chen HS; Napolitano C; Priori SG; Delmar M
Circulation; 2014 Mar; 129(10):1092-103. PubMed ID: 24352520
[TBL] [Abstract][Full Text] [Related]
30. Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.
Abou Ziki MD; Seidelmann SB; Smith E; Atteya G; Jiang Y; Fernandes RG; Marieb MA; Akar JG; Mani A
Clin Genet; 2018 Apr; 93(4):741-751. PubMed ID: 28407228
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. 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]
34. Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death.
Isaacs A; Barysenka A; Ter Bekke RMA; Helderman-van den Enden ATJM; van den Wijngaard A; Volders PGA; Stoll M
Heart Rhythm; 2023 May; 20(5):720-727. PubMed ID: 36764349
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. A common genetic variant within SCN10A modulates cardiac SCN5A expression.
van den Boogaard M; Smemo S; Burnicka-Turek O; Arnolds DE; van de Werken HJ; Klous P; McKean D; Muehlschlegel JD; Moosmann J; Toka O; Yang XH; Koopmann TT; Adriaens ME; Bezzina CR; de Laat W; Seidman C; Seidman JG; Christoffels VM; Nobrega MA; Barnett P; Moskowitz IP
J Clin Invest; 2014 Apr; 124(4):1844-52. PubMed ID: 24642470
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome.
Ishikawa T; Kimoto H; Mishima H; Yamagata K; Ogata S; Aizawa Y; Hayashi K; Morita H; Nakajima T; Nakano Y; Nagase S; Murakoshi N; Kowase S; Ohkubo K; Aiba T; Morimoto S; Ohno S; Kamakura S; Nogami A; Takagi M; Karakachoff M; Dina C; Schott JJ; Yoshiura KI; Horie M; Shimizu W; Nishimura K; Kusano K; Makita N
Eur Heart J; 2021 Jul; 42(29):2854-2863. PubMed ID: 34219138
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]