These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

427 related articles for article (PubMed ID: 35052786)

  • 21. Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
    Singh M; Morin DP; Link MS
    Prog Cardiovasc Dis; 2019; 62(3):227-234. PubMed ID: 31078562
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sudden cardiac death: what is inside our genes?
    Sarkozy A; Brugada P
    Can J Cardiol; 2005 Oct; 21(12):1099-110. PubMed ID: 16234896
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular mechanisms of inherited ventricular arrhythmias.
    Wichter T; Schulze-Bahr E; Eckardt L; Paul M; Levkau B; Meyborg M; Schäfers M; Haverkamp W; Breithardt G
    Herz; 2002 Dec; 27(8):712-39. PubMed ID: 12574890
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects.
    Skinner JR; Winbo A; Abrams D; Vohra J; Wilde AA
    Heart Lung Circ; 2019 Jan; 28(1):22-30. PubMed ID: 30389366
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic arrhythmias.
    Priori SG; Cerrone M
    Ital Heart J; 2005 Mar; 6(3):241-8. PubMed ID: 15875515
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Syncopes and channelopathies].
    Müller-Leisse J; Zormpas C; König T; Duncker D; Veltmann C
    Herzschrittmacherther Elektrophysiol; 2018 Jun; 29(2):171-177. PubMed ID: 29766267
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic causes of sudden cardiac death in the young.
    Mazzanti A; Maragna R; Priori SG
    Curr Opin Cardiol; 2017 May; 32(3):253-261. PubMed ID: 28266935
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ion Channel Disorders and Sudden Cardiac Death.
    Garcia-Elias A; Benito B
    Int J Mol Sci; 2018 Feb; 19(3):. PubMed ID: 29495624
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The electrocardiographic abnormalities in highly trained athletes compared to the genetic study related to causes of unexpected sudden cardiac death.
    Macarie C; Stoian I; Dermengiu D; Barbarii L; Piser IT; Chioncel O; Carp A; Stoian I
    J Med Life; 2009; 2(4):361-72. PubMed ID: 20108749
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
    White JL; Chang AM; Cesar S; Sarquella-Brugada G
    Emergencias; 2018 Jun; 30(3):194-200. PubMed ID: 29687676
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.
    Adler A; Sadek MM; Chan AY; Dell E; Rutberg J; Davis D; Green MS; Spears DA; Gollob MH
    Circ Arrhythm Electrophysiol; 2016 Jan; 9(1):e003440. PubMed ID: 26743238
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.
    Kaufman ES
    Heart Rhythm; 2009 Aug; 6(8 Suppl):S51-5. PubMed ID: 19631908
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia.
    Walsh R; Peters NS; Cook SA; Ware JS
    J Med Genet; 2014 Jan; 51(1):35-44. PubMed ID: 24136861
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders.
    Junttila MJ; Holmström L; Pylkäs K; Mantere T; Kaikkonen K; Porvari K; Kortelainen ML; Pakanen L; Kerkelä R; Myerburg RJ; Huikuri HV
    Circulation; 2018 Jun; 137(25):2716-2726. PubMed ID: 29915098
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cardiac channelopathies and sudden infant death syndrome.
    Tfelt-Hansen J; Winkel BG; Grunnet M; Jespersen T
    Cardiology; 2011; 119(1):21-33. PubMed ID: 21778721
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death.
    Walsh R; Adler A; Amin AS; Abiusi E; Care M; Bikker H; Amenta S; Feilotter H; Nannenberg EA; Mazzarotto F; Trevisan V; Garcia J; Hershberger RE; Perez MV; Sturm AC; Ware JS; Zareba W; Novelli V; Wilde AAM; Gollob MH
    Eur Heart J; 2022 Apr; 43(15):1500-1510. PubMed ID: 34557911
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.
    Hertz CL; Ferrero-Miliani L; Frank-Hansen R; Morling N; Bundgaard H
    Europace; 2015 Mar; 17(3):350-7. PubMed ID: 25345827
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families.
    Kotta MC; Torchio M; Bayliss P; Cohen MC; Quarrell O; Wheeldon N; Marton T; Gentilini D; Crotti L; Coombs RC; Schwartz PJ
    J Am Heart Assoc; 2023 Sep; 12(17):e029100. PubMed ID: 37589201
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and children.
    Tester DJ; Ackerman MJ
    Annu Rev Med; 2009; 60():69-84. PubMed ID: 18928334
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths.
    Farrugia A; Keyser C; Hollard C; Raul JS; Muller J; Ludes B
    Forensic Sci Int; 2015 Sep; 254():5-11. PubMed ID: 26164358
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.