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 *

416 related articles for article (PubMed ID: 26425105)

  • 1. Genetics of inherited primary arrhythmia disorders.
    Spears DA; Gollob MH
    Appl Clin Genet; 2015; 8():215-33. PubMed ID: 26425105
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sudden death and ion channel disease: pathophysiology and implications for management.
    Bastiaenen R; Behr ER
    Heart; 2011 Sep; 97(17):1365-72. PubMed ID: 21685181
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.
    Kumar S; Peters S; Thompson T; Morgan N; Maccicoca I; Trainer A; Zentner D; Kalman JM; Winship I; Vohra JK
    Heart Rhythm; 2013 Nov; 10(11):1653-60. PubMed ID: 23973953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited primary arrhythmia disorders: cardiac channelopathies and sports activity.
    Marrakchi S; Kammoun I; Bennour E; Laroussi L; Ben Miled M; Kachboura S
    Herz; 2020 Apr; 45(2):142-157. PubMed ID: 29744527
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.
    Roston TM; Cunningham T; Lehman A; Laksman ZW; Krahn AD; Sanatani S
    Clin Med Insights Cardiol; 2017; 11():1179546817698134. PubMed ID: 28469493
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Genetic screening in sudden cardiac death in the young can save future lives.
    Stattin EL; Westin IM; Cederquist K; Jonasson J; Jonsson BA; Mörner S; Norberg A; Krantz P; Wisten A
    Int J Legal Med; 2016 Jan; 130(1):59-66. PubMed ID: 26228265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Drug-induced fatal arrhythmias: Acquired long QT and Brugada syndromes.
    Turker I; Ai T; Itoh H; Horie M
    Pharmacol Ther; 2017 Aug; 176():48-59. PubMed ID: 28527921
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Postmortem genetic testing in sudden cardiac death due to ion channelopathies].
    Guan DW; Zhao R
    Fa Yi Xue Za Zhi; 2010 Apr; 26(2):120-7. PubMed ID: 20653139
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry.
    Steinberg C; Padfield GJ; Champagne J; Sanatani S; Angaran P; Andrade JG; Roberts JD; Healey JS; Chauhan VS; Birnie DH; Janzen M; Gerull B; Klein GJ; Leather R; Simpson CS; Seifer C; Talajic M; Gardner M; Krahn AD
    Circ Arrhythm Electrophysiol; 2016 Sep; 9(9):. PubMed ID: 27635072
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances.
    Fernández-Falgueras A; Sarquella-Brugada G; Brugada J; Brugada R; Campuzano O
    Biology (Basel); 2017 Jan; 6(1):. PubMed ID: 28146053
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited ion channel diseases: a brief review.
    Lieve KV; Wilde AA
    Europace; 2015 Oct; 17 Suppl 2():ii1-6. PubMed ID: 26842110
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recent understanding of clinical sequencing and gene-based risk stratification in inherited primary arrhythmia syndrome.
    Aiba T
    J Cardiol; 2019 May; 73(5):335-342. PubMed ID: 30910390
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The genetic and clinical features of cardiac channelopathies.
    Roberts JD; Gollob MH
    Future Cardiol; 2010 Jul; 6(4):491-506. PubMed ID: 20608822
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Arrhythmogenic hereditary syndromes: Brugada Syndrome, long QT syndrome, short QT syndrome and CPVT.
    Schimpf R; Veltmann C; Wolpert C; Borggrefe M
    Minerva Cardioangiol; 2010 Dec; 58(6):623-36. PubMed ID: 21135804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Amplification of spatial dispersion of repolarization underlies sudden cardiac death associated with catecholaminergic polymorphic VT, long QT, short QT and Brugada syndromes.
    Antzelevitch C; Oliva A
    J Intern Med; 2006 Jan; 259(1):48-58. PubMed ID: 16336513
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited arrhythmias: The cardiac channelopathies.
    Behere SP; Weindling SN
    Ann Pediatr Cardiol; 2015; 8(3):210-20. PubMed ID: 26556967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited Cardiac Arrhythmias and Channelopathies.
    Kline J; Costantini O
    Med Clin North Am; 2019 Sep; 103(5):809-820. PubMed ID: 31378327
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.