BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

439 related articles for article (PubMed ID: 23075154)

  • 21. A practical approach to torsade de pointes.
    Roden DM
    Clin Cardiol; 1997 Mar; 20(3):285-90. PubMed ID: 9068917
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Torsade de pointes].
    Haverkamp W; Hördt M; Chen X; Hindricks G; Willems S; Kottkamp H; Rotman B; Brunn J; Borggrefe M; Breithardt G
    Z Kardiol; 1993 Dec; 82(12):763-74. PubMed ID: 8147050
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Rate smoothing with cardiac pacing for preventing torsade de pointes.
    Viskin S; Glikson M; Fish R; Glick A; Copperman Y; Saxon LA
    Am J Cardiol; 2000 Nov; 86(9A):111K-115K. PubMed ID: 11084109
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular predictors of drug-induced prolongation of the QT interval.
    Dilaveris PE
    Curr Med Chem Cardiovasc Hematol Agents; 2005 Apr; 3(2):105-18. PubMed ID: 15853698
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
    Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
    Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Earthquake-Induced Torsade de Pointes in Long-QT Syndrome.
    Nakagawa S; Aiba T; Nakajima K; Kataoka N; Kamakura T; Wada M; Ishibashi K; Yamagata K; Inoue Y; Miyamoto K; Nagase S; Noda T; Miyamoto Y; Yasuda S; Shimizu W; Kusano K
    Circ J; 2019 Aug; 83(9):1968. PubMed ID: 30842358
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Torsade de pointes: the clinical considerations.
    Gowda RM; Khan IA; Wilbur SL; Vasavada BC; Sacchi TJ
    Int J Cardiol; 2004 Jul; 96(1):1-6. PubMed ID: 15203254
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An antibiotic recipe for an arrhythmic disaster.
    McCutcheon K; Manga P
    Cardiovasc J Afr; 2015; 26(3):143-5. PubMed ID: 26592910
    [TBL] [Abstract][Full Text] [Related]  

  • 33. In utero diagnosis of long QT syndrome by magnetocardiography.
    Cuneo BF; Strasburger JF; Yu S; Horigome H; Hosono T; Kandori A; Wakai RT
    Circulation; 2013 Nov; 128(20):2183-91. PubMed ID: 24218437
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
    Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N
    Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [QT prolongation and torsade de pointes tachycardia during therapy with maprotiline. Differential diagnostic and therapeutic aspects].
    Lentini S; Rao ML; Schröder R; Lüderitz B; Bauriedel G
    Dtsch Med Wochenschr; 2001 Dec; 126(49):1396-400. PubMed ID: 11740632
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polymorphic ventricular tachycardia, long Q-T syndrome, and torsades de pointes.
    Passman R; Kadish A
    Med Clin North Am; 2001 Mar; 85(2):321-41. PubMed ID: 11233951
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital long QT syndrome and 2:1 atrioventricular block: an optimistic outcome in the current era.
    Aziz PF; Tanel RE; Zelster IJ; Pass RH; Wieand TS; Vetter VL; Vogel RL; Shah MJ
    Heart Rhythm; 2010 Jun; 7(6):781-5. PubMed ID: 20197117
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [Clinical observation on pause-dependent long QT syndrome and torsade de pointes ventricular tachycardia].
    Song YC
    Zhonghua Xin Xue Guan Bing Za Zhi; 1992 Dec; 20(6):349-51, 389. PubMed ID: 1307971
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital long QT syndrome presenting with a history of epilepsy: misdiagnosis or relationship between channelopathies of the heart and brain?
    Omichi C; Momose Y; Kitahara S
    Epilepsia; 2010 Feb; 51(2):289-92. PubMed ID: 19694797
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.