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.
26. 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]
27. 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]
28. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children. Antzelevitch C J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population. Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276 [TBL] [Abstract][Full Text] [Related]
31. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome. Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A. Paulussen A; Matthijs G; Gewillig M; Verhasselt P; Cohen N; Aerssens J Genet Test; 2003; 7(1):57-61. PubMed ID: 12820704 [TBL] [Abstract][Full Text] [Related]
34. A challenge for mutation specific risk stratification in long QT syndrome type 1. Yagi N; Itoh H; Hisamatsu T; Tomita Y; Kimura H; Fujii Y; Makiyama T; Horie M; Ohno S J Cardiol; 2018 Jul; 72(1):56-65. PubMed ID: 29439887 [TBL] [Abstract][Full Text] [Related]
35. Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction. Biliczki P; Girmatsion Z; Brandes RP; Harenkamp S; Pitard B; Charpentier F; Hébert TE; Hohnloser SH; Baró I; Nattel S; Ehrlich JR Heart Rhythm; 2009 Dec; 6(12):1792-801. PubMed ID: 19959132 [TBL] [Abstract][Full Text] [Related]
36. Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1. Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D Gene; 2012 Dec; 511(1):26-33. PubMed ID: 23000022 [TBL] [Abstract][Full Text] [Related]
38. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2. Cordeiro JM; Perez GJ; Schmitt N; Pfeiffer R; Nesterenko VV; Burashnikov E; Veltmann C; Borggrefe M; Wolpert C; Schimpf R; Antzelevitch C Can J Physiol Pharmacol; 2010 Dec; 88(12):1181-90. PubMed ID: 21164565 [TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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] [Previous] [Next] [New Search]