BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 28781330)

  • 1. Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant - Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping.
    Van Malderen SCH; Daneels D; Kerkhove D; Peeters U; Theuns DAMJ; Droogmans S; Van Camp G; Weytjens C; Biervliet M; Bonduelle M; Van Dooren S; Brugada P
    Circ J; 2017 Dec; 82(1):53-61. PubMed ID: 28781330
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndrome.
    Van Malderen SC; Kerkhove D; Theuns DA; Weytjens C; Droogmans S; Tanaka K; Daneels D; Van Dooren S; Meuwissen M; Bonduelle M; Brugada P; Van Camp G
    Int J Cardiol; 2015 Jul; 191():90-6. PubMed ID: 25965611
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Contraction delay of the RV outflow tract in patients with Brugada syndrome is dependent on the spontaneous ST-segment elevation pattern.
    Rouzet F; Algalarrondo V; Burg S; Nassar P; Sarda-Mantel L; Aouate P; Frank R; Leenhardt A; Fressart V; Charron P; Slama MS; Le Guludec D
    Heart Rhythm; 2011 Dec; 8(12):1905-12. PubMed ID: 21798229
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.
    Meregalli PG; Tan HL; Probst V; Koopmann TT; Tanck MW; Bhuiyan ZA; Sacher F; Kyndt F; Schott JJ; Albuisson J; Mabo P; Bezzina CR; Le Marec H; Wilde AA
    Heart Rhythm; 2009 Mar; 6(3):341-8. PubMed ID: 19251209
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9.
    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]  

  • 10. Copy number variations of SCN5A in Brugada syndrome.
    Sonoda K; Ohno S; Ozawa J; Hayano M; Hattori T; Kobori A; Yahata M; Aburadani I; Watanabe S; Matsumoto Y; Makiyama T; Horie M
    Heart Rhythm; 2018 Aug; 15(8):1179-1188. PubMed ID: 29574140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers.
    Robyns T; Nuyens D; Vandenberk B; Kuiperi C; Corveleyn A; Breckpot J; Garweg C; Ector J; Willems R
    Ann Noninvasive Electrocardiol; 2018 Sep; 23(5):e12548. PubMed ID: 29709101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patient-Specific and Genome-Edited Induced Pluripotent Stem Cell-Derived Cardiomyocytes Elucidate Single-Cell Phenotype of Brugada Syndrome.
    Liang P; Sallam K; Wu H; Li Y; Itzhaki I; Garg P; Zhang Y; Vermglinchan V; Lan F; Gu M; Gong T; Zhuge Y; He C; Ebert AD; Sanchez-Freire V; Churko J; Hu S; Sharma A; Lam CK; Scheinman MM; Bers DM; Wu JC
    J Am Coll Cardiol; 2016 Nov; 68(19):2086-2096. PubMed ID: 27810048
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Genotype-Phenotype Correlation of
    Yamagata K; Horie M; Aiba T; Ogawa S; Aizawa Y; Ohe T; Yamagishi M; Makita N; Sakurada H; Tanaka T; Shimizu A; Hagiwara N; Kishi R; Nakano Y; Takagi M; Makiyama T; Ohno S; Fukuda K; Watanabe H; Morita H; Hayashi K; Kusano K; Kamakura S; Yasuda S; Ogawa H; Miyamoto Y; Kapplinger JD; Ackerman MJ; Shimizu W
    Circulation; 2017 Jun; 135(23):2255-2270. PubMed ID: 28341781
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371* Nonsense Variant in the
    Monasky MM; Micaglio E; Giachino D; Ciconte G; Giannelli L; Locati ET; Ramondini E; Cotugno R; Vicedomini G; Borrelli V; Ghiroldi A; Anastasia L; Pappone C
    Int J Mol Sci; 2019 Nov; 20(22):. PubMed ID: 31698696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ventricular dysfunction in a family with long QT syndrome type 3.
    Hummel YM; Wilde AA; Voors AA; Bugatti S; Hillege HL; van den Berg MP
    Europace; 2013 Oct; 15(10):1516-21. PubMed ID: 23612729
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.