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Journal Abstract Search

368 related items for PubMed ID: 9297927

  • 1. Multi-undulant T-U-wave, sinus bradycardia and long QT syndrome: a possible phenotype of mutant genes controlling the inward potassium rectifiers.
    Shen CT, Wu YC, Yu SS, Wang NK.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(4):267-75. PubMed ID: 9297927
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  • 2. [T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].
    Lupoglazoff JM, Denjoy I, Berthet M, Hainque B, Vaksmann G, Klug D, Villain E, Lucet V, Guicheney P, Coumel P.
    Arch Mal Coeur Vaiss; 2001 May; 94(5):470-8. PubMed ID: 11434015
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  • 4. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
    Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H.
    Circ J; 2003 Jun; 67(6):495-8. PubMed ID: 12808265
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  • 8. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Jun; 49():263-74. PubMed ID: 9509262
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  • 10. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
    Splawski I, Shen J, Timothy KW, Vincent GM, Lehmann MH, Keating MT.
    Genomics; 1998 Jul 01; 51(1):86-97. PubMed ID: 9693036
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  • 11. Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.
    Satler CA, Walsh EP, Vesely MR, Plummer MH, Ginsburg GS, Jacob HJ.
    Am J Med Genet; 1996 Oct 02; 65(1):27-35. PubMed ID: 8914737
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  • 12. Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice.
    Babij P, Askew GR, Nieuwenhuijsen B, Su CM, Bridal TR, Jow B, Argentieri TM, Kulik J, DeGennaro LJ, Spinelli W, Colatsky TJ.
    Circ Res; 1998 Sep 21; 83(6):668-78. PubMed ID: 9742063
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  • 13. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
    Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P.
    J Am Coll Cardiol; 2004 Mar 03; 43(5):826-30. PubMed ID: 14998624
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  • 15. A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.
    Etheridge SP, Compton SJ, Tristani-Firouzi M, Mason JW.
    J Am Coll Cardiol; 2003 Nov 19; 42(10):1777-82. PubMed ID: 14642687
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  • 17. Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
    Allan WC, Timothy K, Vincent GM, Palomaki GE, Neveux LM, Haddow JE.
    J Med Screen; 2001 Nov 19; 8(4):173-7. PubMed ID: 11743032
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  • 18. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns.
    Piippo K, Laitinen P, Swan H, Toivonen L, Viitasalo M, Pasternack M, Paavonen K, Chapman H, Wann KT, Hirvelä E, Sajantila A, Kontula K.
    J Am Coll Cardiol; 2000 Jun 19; 35(7):1919-25. PubMed ID: 10841244
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  • 19. Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
    Johnson WH, Yang P, Yang T, Lau YR, Mostella BA, Wolff DJ, Roden DM, Benson DW.
    Pediatr Res; 2003 May 19; 53(5):744-8. PubMed ID: 12621127
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