BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 21831960)

  • 41. Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.
    Theilade J; Kanters J; Henriksen FL; Gilså-Hansen M; Svendsen JH; Eschen O; Toft E; Reimers JI; Tybjærg-Hansen A; Christiansen M; Jensen HK; Bundgaard H
    Cardiology; 2013; 126(2):131-7. PubMed ID: 23969902
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications.
    Shinwari ZM; Al-Hazzani A; Dzimiri N; Tulbah S; Mallawi Y; Al-Fayyadh M; Al-Hassnan ZN
    Clin Genet; 2013 Apr; 83(4):370-4. PubMed ID: 22708720
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.
    Moss AJ; Shimizu W; Wilde AA; Towbin JA; Zareba W; Robinson JL; Qi M; Vincent GM; Ackerman MJ; Kaufman ES; Hofman N; Seth R; Kamakura S; Miyamoto Y; Goldenberg I; Andrews ML; McNitt S
    Circulation; 2007 May; 115(19):2481-9. PubMed ID: 17470695
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].
    Shi RM; Ma AQ; Zhang YM; Yang C; Huang C; Zhou XH; Liu XH
    Zhonghua Er Ke Za Zhi; 2009 Dec; 47(12):926-30. PubMed ID: 20193146
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.
    Fodstad H; Bendahhou S; Rougier JS; Laitinen-Forsblom PJ; Barhanin J; Abriel H; Schild L; Kontula K; Swan H
    Ann Med; 2006; 38(4):294-304. PubMed ID: 16754261
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genetics of long QT syndrome.
    Tester DJ; Ackerman MJ
    Methodist Debakey Cardiovasc J; 2014; 10(1):29-33. PubMed ID: 24932360
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome.
    Chatrath R; Bell CM; Ackerman MJ
    Pediatr Cardiol; 2004; 25(5):459-65. PubMed ID: 15534720
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome.
    Goldenberg I; Moss AJ; Peterson DR; McNitt S; Zareba W; Andrews ML; Robinson JL; Locati EH; Ackerman MJ; Benhorin J; Kaufman ES; Napolitano C; Priori SG; Qi M; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
    Circulation; 2008 Apr; 117(17):2184-91. PubMed ID: 18427136
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers With Normal QTc Interval: The Value of Sex, T-Wave Morphology, and Mutation Type.
    Platonov PG; McNitt S; Polonsky B; Rosero SZ; Kutyifa V; Huang A; Moss AJ; Zareba W
    Circ Arrhythm Electrophysiol; 2018 Jul; 11(7):e005918. PubMed ID: 30012873
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Risk of recurrent cardiac events after onset of menopause in women with congenital long-QT syndrome types 1 and 2.
    Buber J; Mathew J; Moss AJ; Hall WJ; Barsheshet A; McNitt S; Robinson JL; Zareba W; Ackerman MJ; Kaufman ES; Luria D; Eldar M; Towbin JA; Vincent M; Goldenberg I
    Circulation; 2011 Jun; 123(24):2784-91. PubMed ID: 21632495
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG; Larsen MK; Berge KE; Leren TP; Nissen PH; Olesen MS; Hollegaard MV; Jespersen T; Yuan L; Nielsen N; Haunsø S; Svendsen JH; Wang Y; Kristensen IB; Jensen HK; Tfelt-Hansen J; Banner J
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Long QT syndrome in adults.
    Sauer AJ; Moss AJ; McNitt S; Peterson DR; Zareba W; Robinson JL; Qi M; Goldenberg I; Hobbs JB; Ackerman MJ; Benhorin J; Hall WJ; Kaufman ES; Locati EH; Napolitano C; Priori SG; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
    J Am Coll Cardiol; 2007 Jan; 49(3):329-37. PubMed ID: 17239714
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Risk of death in the long QT syndrome when a sibling has died.
    Kaufman ES; McNitt S; Moss AJ; Zareba W; Robinson JL; Hall WJ; Ackerman MJ; Benhorin J; Locati ET; Napolitano C; Priori SG; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
    Heart Rhythm; 2008 Jun; 5(6):831-6. PubMed ID: 18534367
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Characterization of a KCNQ1/KVLQT1 polymorphism in Asian families with LQT2: implications for genetic testing.
    Sharma D; Glatter KA; Timofeyev V; Tuteja D; Zhang Z; Rodriguez J; Tester DJ; Low R; Scheinman MM; Ackerman MJ; Chiamvimonvat N
    J Mol Cell Cardiol; 2004 Jul; 37(1):79-89. PubMed ID: 15242738
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome.
    Costa J; Lopes CM; Barsheshet A; Moss AJ; Migdalovich D; Ouellet G; McNitt S; Polonsky S; Robinson JL; Zareba W; Ackerman MJ; Benhorin J; Kaufman ES; Platonov PG; Shimizu W; Towbin JA; Vincent GM; Wilde AA; Goldenberg I
    Heart Rhythm; 2012 Jun; 9(6):892-8. PubMed ID: 22293141
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.