BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

305 related articles for article (PubMed ID: 26715165)

  • 1. The genetics underlying acquired long QT syndrome: impact for genetic screening.
    Itoh H; Crotti L; Aiba T; Spazzolini C; Denjoy I; Fressart V; Hayashi K; Nakajima T; Ohno S; Makiyama T; Wu J; Hasegawa K; Mastantuono E; Dagradi F; Pedrazzini M; Yamagishi M; Berthet M; Murakami Y; Shimizu W; Guicheney P; Schwartz PJ; Horie M
    Eur Heart J; 2016 May; 37(18):1456-64. PubMed ID: 26715165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
    Paulussen AD; Gilissen RA; Armstrong M; Doevendans PA; Verhasselt P; Smeets HJ; Schulze-Bahr E; Haverkamp W; Breithardt G; Cohen N; Aerssens J
    J Mol Med (Berl); 2004 Mar; 82(3):182-8. PubMed ID: 14760488
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The diagnostic role of T wave morphology biomarkers in congenital and acquired long QT syndrome: A systematic review.
    Tardo DT; Peck M; Subbiah RN; Vandenberg JI; Hill AP
    Ann Noninvasive Electrocardiol; 2023 Jan; 28(1):e13015. PubMed ID: 36345173
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.
    Fujii Y; Matsumoto Y; Hayashi K; Ding WG; Tomita Y; Fukumoto D; Wada Y; Ichikawa M; Sonoda K; Ozawa J; Makiyama T; Ohno S; Yamagishi M; Matsuura H; Horie M; Itoh H
    J Cardiol; 2017 Jul; 70(1):74-79. PubMed ID: 27816319
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
    Itoh H; Sakaguchi T; Ding WG; Watanabe E; Watanabe I; Nishio Y; Makiyama T; Ohno S; Akao M; Higashi Y; Zenda N; Kubota T; Mori C; Okajima K; Haruna T; Miyamoto A; Kawamura M; Ishida K; Nagaoka I; Oka Y; Nakazawa Y; Yao T; Jo H; Sugimoto Y; Ashihara T; Hayashi H; Ito M; Imoto K; Matsuura H; Horie M
    Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):511-23. PubMed ID: 19843919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Post-acute management of the acquired long QT syndrome.
    Barra S; Agarwal S; Begley D; Providência R
    Postgrad Med J; 2014 Jun; 90(1064):348-58. PubMed ID: 24696523
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
    Ghouse J; Have CT; Weeke P; Bille Nielsen J; Ahlberg G; Balslev-Harder M; Appel EV; Skaaby T; Olesen SP; Grarup N; Linneberg A; Pedersen O; Haunsø S; Hastrup Svendsen J; Hansen T; Kanters JK; Salling Olesen M
    Eur Heart J; 2015 Oct; 36(37):2523-9. PubMed ID: 26159999
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
    Zhang X; Chen S; Zhang L; Liu M; Redfearn S; Bryant RM; Oberti C; Vincent GM; Wang QK
    BMC Med Genet; 2008 Sep; 9():87. PubMed ID: 18808722
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: a long-term follow-up.
    Mönnig G; Köbe J; Löher A; Wasmer K; Milberg P; Zellerhoff S; Pott C; Zumhagen S; Radu R; Scheld HH; Haverkamp W; Schulze-Bahr E; Eckardt L
    Europace; 2012 Mar; 14(3):396-401. PubMed ID: 21979994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. End-recovery QTc: a useful metric for assessing genetic variants of unknown significance in long-QT syndrome.
    Obeyesekere MN; Sy RW; Klein GJ; Gula LJ; Modi S; Conacher S; Leong-Sit P; Skanes AC; Yee R; Krahn AD
    J Cardiovasc Electrophysiol; 2012 Jun; 23(6):637-42. PubMed ID: 22429796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acquired long QT syndrome in hospitalized patients.
    Yu H; Zhang L; Liu J; Liu Y; Kowey PR; Zhang Y; Chen Y; Wei Y; Gao L; Li H; Du J; Xia Y
    Heart Rhythm; 2017 Jul; 14(7):974-978. PubMed ID: 28323171
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic basis of long QT and short QT syndromes: a mutation update.
    Hedley PL; Jørgensen P; Schlamowitz S; Wangari R; Moolman-Smook J; Brink PA; Kanters JK; Corfield VA; Christiansen M
    Hum Mutat; 2009 Nov; 30(11):1486-511. PubMed ID: 19862833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome.
    Gray B; Baruteau AE; Antolin AA; Pittman A; Sarganas G; Molokhia M; Blom MT; Bastiaenen R; Bardai A; Priori SG; Napolitano C; Weeke PE; Shakir SA; Haverkamp W; Mestres J; Winkel BG; Witney AA; Chis-Ster I; Sangaralingam A; Camm AJ; Tfelt-Hansen J; Roden DM; Tan HL; Garbe E; Sturkenboom M; Behr ER
    Circ Genom Precis Med; 2022 Feb; 15(1):e003391. PubMed ID: 35113648
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Perioperative treatment of patients with long QT syndrome].
    Krönauer T; Friederich P
    Anaesthesist; 2015 Aug; 64(8):625-37; quiz 638-9. PubMed ID: 26260197
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A novel KCNQ1 mutation in Chinese with congenital long QT syndrome].
    Liang L; Du ZD; Cai LL; Wu JX; Zheng T; Qi TX
    Zhonghua Er Ke Za Zhi; 2003 Oct; 41(10):724-7. PubMed ID: 14731347
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence and risk factors for acquired long QT syndrome in the emergency department: a retrospective observational study.
    Fernandes DA; Camões GF; Ferreira D; Queijo C; Fontes-Ribeiro C; Gonçalves L; Pina R; António N
    World J Emerg Med; 2023; 14(6):454-461. PubMed ID: 37969211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital long QT syndrome: severe torsades de pointes provoked by epinephrine in a digenic mutation carrier.
    Tan VH; Duff H; Kuriachan V; Gerull B
    Heart Lung; 2014; 43(6):541-5. PubMed ID: 25236808
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Long QT syndrome. History, genetics, clinical symptoms, causes and therapy].
    Krönauer T; Friederich P
    Anaesthesist; 2015 Aug; 64(8):586-95. PubMed ID: 26250931
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Relation of increased short-term variability of QT interval to congenital long-QT syndrome.
    Hinterseer M; Beckmann BM; Thomsen MB; Pfeufer A; Dalla Pozza R; Loeff M; Netz H; Steinbeck G; Vos MA; Kääb S
    Am J Cardiol; 2009 May; 103(9):1244-8. PubMed ID: 19406266
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.