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Journal Abstract Search

106 related items for PubMed ID: 2236786

  • 1. [A child affected by the Romano-Ward syndrome born of a mother with the Jervell and Lange-Nielsen syndrome].
    Sánchez Cascos A, Sánchez Pernaute R, Cifuentes S.
    Rev Esp Cardiol; 1990; 43(6):406-7. PubMed ID: 2236786
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  • 5. Cochlear implantation in children with Jervell, Lange-Nielsen syndrome.
    Daneshi A, Ghassemi MM, Talee M, Hassanzadeh S.
    J Laryngol Otol; 2008 Mar; 122(3):314-7. PubMed ID: 17498328
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  • 6. Hereditary long QT syndrome in pregnancy: antenatal and intrapartum management options.
    Papantoniou N, Katsoulis I, Papageorgiou I, Antsaklis A.
    J Matern Fetal Neonatal Med; 2007 May; 20(5):419-21. PubMed ID: 17674248
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  • 7. [Hereditary prolonged QT interval (Romano Ward syndrome) in obstetric management].
    Heidegger H, von Hugo R, Plötz J.
    Geburtshilfe Frauenheilkd; 1993 Mar; 53(3):201-3. PubMed ID: 8467990
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  • 9. Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
    Wei J, Fish FA, Myerburg RJ, Roden DM, George AL.
    Hum Mutat; 2000 Apr; 15(4):387-8. PubMed ID: 10737999
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  • 10. [Long QT--a polymorphic syndrome].
    Swan H.
    Duodecim; 1998 Apr; 114(19):1905-13. PubMed ID: 11717744
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  • 11. [Jervell and Lange-Nielsen cardioauditory syndrome].
    Ferreira M das G, da Cunha GP, Marçallo FA.
    Arq Bras Cardiol; 1986 Sep; 47(3):173-9. PubMed ID: 3593016
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  • 12. Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.
    Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P.
    Eur J Hum Genet; 1998 Sep; 6(2):129-33. PubMed ID: 9781056
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  • 13. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
    Bhuiyan ZA, Momenah TS, Amin AS, Al-Khadra AS, Alders M, Wilde AA, Mannens MM.
    Prog Biophys Mol Biol; 2008 Sep; 98(2-3):319-27. PubMed ID: 19027783
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  • 16. [Jervell and Lange-Nielsen syndrome].
    Aoki T.
    Ryoikibetsu Shokogun Shirizu; 1996 Sep; (12):188-91. PubMed ID: 9047439
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  • 17. KCNE1 mutations cause jervell and Lange-Nielsen syndrome.
    Schulze-Bahr E, Wang Q, Wedekind H, Haverkamp W, Chen Q, Sun Y, Rubie C, Hördt M, Towbin JA, Borggrefe M, Assmann G, Qu X, Somberg JC, Breithardt G, Oberti C, Funke H.
    Nat Genet; 1997 Nov; 17(3):267-8. PubMed ID: 9354783
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  • 19. [Molecular genetics of the long QT syndrome: clinical aspects].
    Sepp R, Csanády M.
    Orv Hetil; 1999 Nov 21; 140(47):2633-8. PubMed ID: 10613047
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  • 20. [Hereditary prolonged QT interval (Romano-Ward syndrome) in a female patient with non-elective cesarean section].
    Plötz J, Heidegger H, von Hugo R, Grohmann H, Deeg KH.
    Anaesthesist; 1992 Feb 21; 41(2):88-92. PubMed ID: 1562098
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