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Journal Abstract Search

594 related items for PubMed ID: 18808722

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  • 22. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C, Zhao Q, Su T, Tang S, Lv G, Liu H, Quan L, Cheng J.
    Forensic Sci Int; 2013 Sep 10; 231(1-3):82-7. PubMed ID: 23890619
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  • 24. 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 10; 131(2):333-338. PubMed ID: 27613431
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  • 28. 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 Mar 10; 38(4):294-304. PubMed ID: 16754261
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  • 29. [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 10; 47(12):926-30. PubMed ID: 20193146
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  • 33. Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations.
    Leong IU, Stuckey A, Lai D, Skinner JR, Love DR.
    BMC Med Genet; 2015 May 13; 16():34. PubMed ID: 25967940
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  • 34. Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
    Koponen M, Marjamaa A, Hiippala A, Happonen JM, Havulinna AS, Salomaa V, Lahtinen AM, Hintsa T, Viitasalo M, Toivonen L, Kontula K, Swan H.
    Circ Arrhythm Electrophysiol; 2015 Aug 13; 8(4):815-23. PubMed ID: 26063740
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  • 35. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.
    Liu L, Hayashi K, Kaneda T, Ino H, Fujino N, Uchiyama K, Konno T, Tsuda T, Kawashiri MA, Ueda K, Higashikata T, Shuai W, Kupershmidt S, Higashida H, Yamagishi M.
    Heart Rhythm; 2013 Jan 13; 10(1):61-7. PubMed ID: 23010577
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  • 36. Long QT syndrome-associated mutations in intrauterine fetal death.
    Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ.
    JAMA; 2013 Apr 10; 309(14):1473-82. PubMed ID: 23571586
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  • 37. 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 03; 120(18):1752-60. PubMed ID: 19841300
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  • 38. 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 03; 8(5):501-510. PubMed ID: 25890583
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  • 39. [Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].
    Du R, Ren FX, Yang JG, Yuan GH, Zhang SY, Kang CL, Li W, Gui L, Li J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Jun 03; 27(3):289-94. PubMed ID: 16038262
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  • 40. Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.
    Liu W, Hu D, Li C, Li P, Li Y, Li Z, Li L, Qin X, Dong W, Qi Y, Chen S, Wang Q.
    Chin Med J (Engl); 2003 Sep 03; 116(9):1333-5. PubMed ID: 14527360
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