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 *

172 related articles for article (PubMed ID: 19184172)

  • 21. 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]  

  • 22. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS; Yang YW; Lin YN; Lin KH; Chang KC; Chang JG
    Int Heart J; 2015; 56(4):450-3. PubMed ID: 26118593
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
    Altmann HM; Tester DJ; Will ML; Middha S; Evans JM; Eckloff BW; Ackerman MJ
    Circulation; 2015 Jun; 131(23):2051-60. PubMed ID: 25922419
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Atrial Fibrillation in Long QT Syndrome by Genotype.
    Platonov PG; McNitt S; Polonsky B; Rosero SZ; Zareba W
    Circ Arrhythm Electrophysiol; 2019 Oct; 12(10):e007213. PubMed ID: 31610692
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
    Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
    J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
    Koponen M; Marjamaa A; Hiippala A; Happonen JM; Havulinna AS; Salomaa V; Lahtinen AM; Hintsa T; Viitasalo M; Toivonen L; Kontula K; Swan H
    Circ Arrhythm Electrophysiol; 2015 Aug; 8(4):815-23. PubMed ID: 26063740
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing.
    Andrsova I; Novotny T; Kadlecova J; Bittnerova A; Vit P; Florianova A; Sisakova M; Gaillyova R; Manouskova L; Spinar J
    J Electrocardiol; 2012; 45(6):746-51. PubMed ID: 22727609
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.
    Horigome H; Nagashima M; Sumitomo N; Yoshinaga M; Ushinohama H; Iwamoto M; Shiono J; Ichihashi K; Hasegawa S; Yoshikawa T; Matsunaga T; Goto H; Waki K; Arima M; Takasugi H; Tanaka Y; Tauchi N; Ikoma M; Inamura N; Takahashi H; Shimizu W; Horie M
    Circ Arrhythm Electrophysiol; 2010 Feb; 3(1):10-7. PubMed ID: 19996378
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pediatric Cohort With Long QT Syndrome - KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms.
    Ozawa J; Ohno S; Hisamatsu T; Itoh H; Makiyama T; Suzuki H; Saitoh A; Horie M
    Circ J; 2016; 80(3):696-702. PubMed ID: 26823142
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole-exome sequencing and electrophysiological study reveal a novel loss-of-function mutation of KCNA10 in epinephrine provoked long QT syndrome with familial history of sudden cardiac death.
    Huang S; Chen J; Song M; Yu Y; Geng J; Lin D; Yang J; Wu J; Li K; Yu Y; Wang J; Hu L; Shan Q; Wang J; Chen P; Chen F
    Leg Med (Tokyo); 2023 May; 62():102245. PubMed ID: 36965351
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Aborted Cardiac Arrest in LQT2 Related to Novel
    Bileišienė N; Barysienė J; Mikštienė V; Preikšaitienė E; Marinskis G; Keževičiūtė M; Utkus A; Aidietis A
    Medicina (Kaunas); 2021 Jul; 57(7):. PubMed ID: 34357002
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Unexplained fainting, near drowning and unusual seizures in childhood: screening for long QT syndrome in New Zealand families.
    Bradley T; Dixon J; Easthope R
    N Z Med J; 1999 Aug; 112(1093):299-302. PubMed ID: 10493429
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.
    Itoh H; Berthet M; Fressart V; Denjoy I; Maugenre S; Klug D; Mizusawa Y; Makiyama T; Hofman N; Stallmeyer B; Zumhagen S; Shimizu W; Wilde AA; Schulze-Bahr E; Horie M; Tezenas du Montcel S; Guicheney P
    Eur J Hum Genet; 2016 Aug; 24(8):1160-6. PubMed ID: 26669661
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome.
    Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Kaneda T; Mabuchi H; Sumita R; Oshima T; Hoshi N; Higashida H
    Clin Sci (Lond); 2005 Feb; 108(2):143-50. PubMed ID: 15500450
    [TBL] [Abstract][Full Text] [Related]  

  • 35. QT interval prolongation and risk for cardiac events in genotyped LQTS-index children.
    Wedekind H; Burde D; Zumhagen S; Debus V; Burkhardtsmaier G; Mönnig G; Breithardt G; Schulze-Bahr E
    Eur J Pediatr; 2009 Sep; 168(9):1107-15. PubMed ID: 19101729
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Risk of Cardiac Events Associated With Antidepressant Therapy in Patients With Long QT Syndrome.
    Wang M; Szepietowska B; Polonsky B; McNitt S; Moss AJ; Zareba W; Auerbach DS
    Am J Cardiol; 2018 Jan; 121(2):182-187. PubMed ID: 29174490
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Long QT syndrome in children.
    Zareba W; Moss AJ
    J Electrocardiol; 2001; 34 Suppl():167-71. PubMed ID: 11781951
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical aspects of the three major genetic forms of long QT syndrome (LQT1, LQT2, LQT3).
    Kutyifa V; Daimee UA; McNitt S; Polonsky B; Lowenstein C; Cutter K; Lopes C; Zareba W; Moss AJ
    Ann Noninvasive Electrocardiol; 2018 May; 23(3):e12537. PubMed ID: 29504689
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.