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 *

287 related articles for article (PubMed ID: 21831960)

  • 101. Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.
    Trolle C; Mortensen KH; Pedersen LN; Berglund A; Jensen HK; Andersen NH; Gravholt CH
    PLoS One; 2013; 8(7):e69614. PubMed ID: 23936059
    [TBL] [Abstract][Full Text] [Related]  

  • 102. Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.
    J E; T D; M S; M KN; J D; M NW
    Int J Legal Med; 2017 Mar; 131(2):333-338. PubMed ID: 27613431
    [TBL] [Abstract][Full Text] [Related]  

  • 103. 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]  

  • 104. Long QT syndrome: a double hit hurts more.
    Wilde AA
    Heart Rhythm; 2010 Oct; 7(10):1419-20. PubMed ID: 20601150
    [No Abstract]   [Full Text] [Related]  

  • 105. Genotype-specific QT correction for heart rate and the risk of life-threatening cardiac events in adolescents with congenital long-QT syndrome.
    Barsheshet A; Peterson DR; Moss AJ; Schwartz PJ; Kaufman ES; McNitt S; Polonsky S; Buber J; Zareba W; Robinson JL; Ackerman MJ; Benhorin J; Towbin JA; Vincent GM; Zhang L; Goldenberg I
    Heart Rhythm; 2011 Aug; 8(8):1207-13. PubMed ID: 21397043
    [TBL] [Abstract][Full Text] [Related]  

  • 106. Phenotypes of Overdiagnosed Long QT Syndrome.
    Bains S; Neves R; Bos JM; Giudicessi JR; MacIntyre C; Ackerman MJ
    J Am Coll Cardiol; 2023 Feb; 81(5):477-486. PubMed ID: 36725176
    [TBL] [Abstract][Full Text] [Related]  

  • 107. KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences.
    Ke Z; Li C; Bai G; Tan L; Wang J; Zhou M; Zhou J; Chen SY; Dong X
    Clinics (Sao Paulo); 2023; 78():100285. PubMed ID: 37783170
    [TBL] [Abstract][Full Text] [Related]  

  • 108. Effectiveness of Implantable Cardioverter-Defibrillators to Reduce Mortality in Patients With Long QT Syndrome.
    Wang M; Peterson DR; Rosero S; McNitt S; Rich DQ; Seplaki CL; Polonsky B; Goldenberg I; Zareba W
    J Am Coll Cardiol; 2021 Nov; 78(21):2076-2088. PubMed ID: 34794689
    [TBL] [Abstract][Full Text] [Related]  

  • 109. Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.
    Stattin EL; Boström IM; Winbo A; Cederquist K; Jonasson J; Jonsson BA; Diamant UB; Jensen SM; Rydberg A; Norberg A
    BMC Cardiovasc Disord; 2012 Oct; 12():95. PubMed ID: 23098067
    [TBL] [Abstract][Full Text] [Related]  

  • 110. Association Between Syncope Trigger Type and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome.
    Younis A; Bos JM; Zareba W; Aktas MK; Wilde AAM; Tabaja C; Bodurian C; Tobert KE; McNitt S; Polonsky B; Shimizu W; Ackerman MJ; Goldenberg I
    JAMA Cardiol; 2023 Aug; 8(8):775-783. PubMed ID: 37436769
    [TBL] [Abstract][Full Text] [Related]  

  • 111. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.
    Schwartz PJ; Priori SG; Locati EH; Napolitano C; Cantù F; Towbin JA; Keating MT; Hammoude H; Brown AM; Chen LS; Colatsky TJ
    Circulation; 1995 Dec; 92(12):3381-6. PubMed ID: 8521555
    [TBL] [Abstract][Full Text] [Related]  

  • 112. 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]  

  • 113. Effectiveness of beta-blockers depending on the genotype of congenital long-QT syndrome: A meta-analysis.
    Ahn J; Kim HJ; Choi JI; Lee KN; Shim J; Ahn HS; Kim YH
    PLoS One; 2017; 12(10):e0185680. PubMed ID: 29059199
    [TBL] [Abstract][Full Text] [Related]  

  • 114. Molecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?
    Kamei S; Sato N; Harayama Y; Nunotani M; Takatsu K; Shiozaki T; Hayashi T; Asamura H
    J Hum Genet; 2014 Feb; 59(2):95-9. PubMed ID: 24284363
    [TBL] [Abstract][Full Text] [Related]  

  • 115. Risk of life-threatening cardiac events among patients with long QT syndrome and multiple mutations.
    Mullally J; Goldenberg I; Moss AJ; Lopes CM; Ackerman MJ; Zareba W; McNitt S; Robinson JL; Benhorin J; Kaufman ES; Towbin JA; Barsheshet A
    Heart Rhythm; 2013 Mar; 10(3):378-82. PubMed ID: 23174487
    [TBL] [Abstract][Full Text] [Related]  

  • 116. Do LQTS gene single nucleotide polymorphisms alter QTc intervals at rest and during exercise stress testing?
    Aziz PF; Wieand TS; Ganley J; Henderson J; McBride M; Shah MJ
    Ann Noninvasive Electrocardiol; 2013 May; 18(3):288-93. PubMed ID: 23714088
    [TBL] [Abstract][Full Text] [Related]  

  • 117. Clinical and electrophysiological features of Japanese pediatric long QT syndrome patients with KCNQ1 mutations.
    Yasuda K; Hayashi G; Horie A; Taketani T; Yamaguchi S
    Pediatr Int; 2008 Oct; 50(5):611-4. PubMed ID: 19261104
    [TBL] [Abstract][Full Text] [Related]  

  • 118. Long QT molecular autopsy in sudden infant death syndrome.
    Glengarry JM; Crawford J; Morrow PL; Stables SR; Love DR; Skinner JR
    Arch Dis Child; 2014 Jul; 99(7):635-40. PubMed ID: 24596401
    [TBL] [Abstract][Full Text] [Related]  

  • 119. Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort.
    Chang RK; Lan YT; Silka MJ; Morrow H; Kwong A; Smith-Lang J; Wallerstein R; Lin HJ
    J Pediatr; 2014 Mar; 164(3):590-5.e1-3. PubMed ID: 24388587
    [TBL] [Abstract][Full Text] [Related]  

  • 120. Common variants in cardiac ion channel genes are associated with sudden cardiac death.
    Albert CM; MacRae CA; Chasman DI; VanDenburgh M; Buring JE; Manson JE; Cook NR; Newton-Cheh C
    Circ Arrhythm Electrophysiol; 2010 Jun; 3(3):222-9. PubMed ID: 20400777
    [TBL] [Abstract][Full Text] [Related]  

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