BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 19038855)

  • 1. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy.
    Johnson JN; Hofman N; Haglund CM; Cascino GD; Wilde AA; Ackerman MJ
    Neurology; 2009 Jan; 72(3):224-31. PubMed ID: 19038855
    [TBL] [Abstract][Full Text] [Related]  

  • 2. KCNH2 variants in a family with epilepsy and long QT syndrome: A case report and literature review.
    Zhou Y; Hao N; Sander JW; Lin X; Xiong W; Zhou D
    Epileptic Disord; 2023 Aug; 25(4):492-499. PubMed ID: 36946251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients.
    Shimizu W; Makimoto H; Yamagata K; Kamakura T; Wada M; Miyamoto K; Inoue-Yamada Y; Okamura H; Ishibashi K; Noda T; Nagase S; Miyazaki A; Sakaguchi H; Shiraishi I; Makiyama T; Ohno S; Itoh H; Watanabe H; Hayashi K; Yamagishi M; Morita H; Yoshinaga M; Aizawa Y; Kusano K; Miyamoto Y; Kamakura S; Yasuda S; Ogawa H; Tanaka T; Sumitomo N; Hagiwara N; Fukuda K; Ogawa S; Aizawa Y; Makita N; Ohe T; Horie M; Aiba T
    JAMA Cardiol; 2019 Mar; 4(3):246-254. PubMed ID: 30758498
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
    Tester DJ; Will ML; Haglund CM; Ackerman MJ
    Heart Rhythm; 2005 May; 2(5):507-17. PubMed ID: 15840476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
    Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
    Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
    Wong JA; Gula LJ; Klein GJ; Yee R; Skanes AC; Krahn AD
    Circ Arrhythm Electrophysiol; 2010 Apr; 3(2):120-5. PubMed ID: 20071715
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
    Zareba W; Moss AJ; Locati EH; Lehmann MH; Peterson DR; Hall WJ; Schwartz PJ; Vincent GM; Priori SG; Benhorin J; Towbin JA; Robinson JL; Andrews ML; Napolitano C; Timothy K; Zhang L; Medina A;
    J Am Coll Cardiol; 2003 Jul; 42(1):103-9. PubMed ID: 12849668
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence and spectrum of electroencephalogram-identified epileptiform activity among patients with long QT syndrome.
    Anderson JH; Bos JM; Cascino GD; Ackerman MJ
    Heart Rhythm; 2014 Jan; 11(1):53-7. PubMed ID: 24103226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
    Tester DJ; Benton AJ; Train L; Deal B; Baudhuin LM; Ackerman MJ
    Am J Cardiol; 2010 Oct; 106(8):1124-8. PubMed ID: 20920651
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ; Cronk LB; Carr JL; Schulz V; Salisbury BA; Judson RS; Ackerman MJ
    Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiac Mechanical Alterations and Genotype Specific Differences in Subjects With Long QT Syndrome.
    Leren IS; Hasselberg NE; Saberniak J; Håland TF; Kongsgård E; Smiseth OA; Edvardsen T; Haugaa KH
    JACC Cardiovasc Imaging; 2015 May; 8(5):501-510. PubMed ID: 25890583
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
    Kapa S; Tester DJ; Salisbury BA; Harris-Kerr C; Pungliya MS; Alders M; Wilde AA; Ackerman MJ
    Circulation; 2009 Nov; 120(18):1752-60. PubMed ID: 19841300
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular biology of the long QT syndrome: impact on management.
    Priori SG; Napolitano C; Paganini V; Cantù F; Schwartz PJ
    Pacing Clin Electrophysiol; 1997 Aug; 20(8 Pt 2):2052-7. PubMed ID: 9272507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant.
    Tiron C; Campuzano O; Pérez-Serra A; Mademont I; Coll M; Allegue C; Iglesias A; Partemi S; Striano P; Oliva A; Brugada R
    Seizure; 2015 Feb; 25():65-7. PubMed ID: 25645639
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.
    Koponen M; Havulinna AS; Marjamaa A; Tuiskula AM; Salomaa V; Laitinen-Forsblom PJ; Piippo K; Toivonen L; Kontula K; Viitasalo M; Swan H
    BMC Med Genet; 2018 Apr; 19(1):56. PubMed ID: 29622001
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome.
    Eddy CA; MacCormick JM; Chung SK; Crawford JR; Love DR; Rees MI; Skinner JR; Shelling AN
    Heart Rhythm; 2008 Sep; 5(9):1275-81. PubMed ID: 18774102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. KCNH2 gene mutation: a potential link between epilepsy and long QT-2 syndrome.
    Zamorano-León JJ; Yañez R; Jaime G; Rodriguez-Sierra P; Calatrava-Ledrado L; Alvarez-Granada RR; Mateos-Cáceres PJ; Macaya C; López-Farré AJ
    J Neurogenet; 2012 Sep; 26(3-4):382-6. PubMed ID: 22515331
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
    Tester DJ; Ackerman MJ
    J Am Coll Cardiol; 2007 Jan; 49(2):240-6. PubMed ID: 17222736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.
    Choi G; Kopplin LJ; Tester DJ; Will ML; Haglund CM; Ackerman MJ
    Circulation; 2004 Oct; 110(15):2119-24. PubMed ID: 15466642
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant.
    Tobert KE; Tester DJ; Zhou W; Haglund-Turnquist CM; Giudicessi JR; Ackerman MJ
    Heart Rhythm; 2022 Jun; 19(6):998-1007. PubMed ID: 35144019
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.