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There are 7347 results for: content related to: Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications

  1. You have free access to this content
    Long QT syndrome: beyond the causal mutation

    The Journal of Physiology

    Volume 591, Issue 17, September 2013, Pages: 4125–4139, Ahmad S. Amin, Yigal M. Pinto and Arthur A. M. Wilde

    Version of Record online : 19 JUL 2013, DOI: 10.1113/jphysiol.2013.254920

  2. Breath Holding Spells in Children with Long QT Syndrome

    Congenital Heart Disease

    Volume 10, Issue 4, July/August 2015, Pages: 354–361, Jeffrey A. Robinson, J. Martijn Bos, Susan P. Etheridge and Michael J. Ackerman

    Version of Record online : 27 APR 2015, DOI: 10.1111/chd.12262

  3. Mutations at KCNQ1 and an unknown locus cause long QT syndrome in a large Australian family: Implications for genetic testing

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 3, March 2010, Pages: 613–621, Kim M. Summers, Nilesh J. Bokil, Foong Teng Lu, Jiun Tsuen Low, John M. Baisden, David Duffy and Dorothy J. Radford

    Version of Record online : 22 FEB 2010, DOI: 10.1002/ajmg.a.33274

  4. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death

    Clinical Genetics

    Volume 63, Issue 4, April 2003, Pages: 273–282, S Chen, L Zhang, RM Bryant, GM Vincent, M Flippin, JC Lee, E Brown, F Zimmerman, R Rozich, P Szafranski, C Oberti, R Sterba, D Marangi, PJ Tchou, MK Chung and Q Wang

    Version of Record online : 22 APR 2003, DOI: 10.1034/j.1399-0004.2003.00048.x

  5. Beckwith–Wiedemann syndrome and long QT syndrome due to familial-balanced translocation t(11;17)(p15.5;q21.3) involving the KCNQ1 gene

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 78–81, S Kaltenbach, Y Capri, S Rossignol, I Denjoy, S Soudée, A Aboura, C Baumann and A Verloes

    Version of Record online : 14 NOV 2012, DOI: 10.1111/cge.12038

  6. LQTS in Northern BC: homozygosity for KCNQ1V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 85–90, H.A. Jackson, S. McIntosh, B. Whittome, S. Asuri, B. Casey, C. Kerr, A. Tang and L.T. Arbour

    Version of Record online : 30 JUL 2013, DOI: 10.1111/cge.12235

  7. Clinical and electrophysiological features of Japanese pediatric long QT syndrome patients with KCNQ1 mutations

    Pediatrics International

    Volume 50, Issue 5, October 2008, Pages: 611–614, Kenji Yasuda, George Hayashi, Akiyoshi Horie, Takeshi Taketani and Seiji Yamaguchi

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1442-200X.2008.02623.x

  8. Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-QT Syndrome Genotype–Phenotype Correlations of the KCNQ1(S349W) Mutation

    Journal of Cardiovascular Electrophysiology

    Volume 22, Issue 2, February 2011, Pages: 193–200, SAMUEL HORR, ILAN GOLDENBERG, ARTHUR J. MOSS, JIN O-UCHI, ALON BARSHESHET, HEATHER CONNELLY, DANIEL A. GRAY, WOJCIECH ZAREBA and COELI M. B. LOPES

    Version of Record online : 19 JUL 2010, DOI: 10.1111/j.1540-8167.2010.01852.x

  9. Identification of Low-Risk Adult Congenital LQTS Patients

    Journal of Cardiovascular Electrophysiology

    Volume 26, Issue 8, August 2015, Pages: 853–858, CLAIRE ZHANG, VALENTINA KUTYIFA, SCOTT MCNITT, WOJCIECH ZAREBA, ILAN GOLDENBERG and ARTHUR J. MOSS

    Version of Record online : 28 MAY 2015, DOI: 10.1111/jce.12686

  10. End-Recovery QTc: A Useful Metric for Assessing Genetic Variants of Unknown Significance in Long-QT syndrome

    Journal of Cardiovascular Electrophysiology

    Volume 23, Issue 6, June 2012, Pages: 637–642, MANOJ N. OBEYESEKERE, RAYMOND W. SY, GEORGE J. KLEIN, LORNE J. GULA, SIMON MODI, SUSAN CONACHER, PETER LEONG-SIT, ALLAN C. SKANES, RAYMOND YEE and ANDREW D. KRAHN

    Version of Record online : 19 MAR 2012, DOI: 10.1111/j.1540-8167.2011.02265.x

  11. Catecholamine-Provoked Microvoltage T Wave Alternans in Genotyped Long QT Syndrome

    Pacing and Clinical Electrophysiology

    Volume 26, Issue 8, August 2003, Pages: 1660–1667, JAN NEMEC, MICHAEL J. ACKERMAN, DAVID J. TESTER, JOSEPH HEJLIK and WIN-KUANG SHEN

    Version of Record online : 24 JUL 2003, DOI: 10.1046/j.1460-9592.2003.t01-1-00249.x

  12. Instability of KCNE1-D85N that Causes Long QT Syndrome: Stabilization by Verapamil

    Pacing and Clinical Electrophysiology

    Volume 37, Issue 7, July 2014, Pages: 853–863, SHINJI SAKATA, YASUTAKA KURATA, PEILI LI, TOMOMI NOTSU, KUMI MORIKAWA, JUNICHIRO MIAKE, KATSUMI HIGAKI, YASUTAKA YAMAMOTO, AKIO YOSHIDA, YASUAKI SHIRAYOSHI, KAZUHIRO YAMAMOTO, MINORU HORIE, HARUAKI NINOMIYA, SUSUMU KANZAKI and ICHIRO HISATOME

    Version of Record online : 5 FEB 2014, DOI: 10.1111/pace.12360

  13. The Prevalence of Mutations in KCNQ1, KCNH2, and SCN5A in an Unselected National Cohort of Young Sudden Unexplained Death Cases

    Journal of Cardiovascular Electrophysiology

    Volume 23, Issue 10, October 2012, Pages: 1092–1098, BO GREGERS WINKEL, MAIKEN KUDAHL LARSEN, KNUT ERIK BERGE, TROND PAUL LEREN, PETER HENRIK NISSEN, MORTEN SALLING OLESEN, MADS VILHELM HOLLEGAARD, THOMAS JESPERSEN, LEI YUAN, NIKOLAJ NIELSEN, STIG HAUNSØ, JESPER HASTRUP SVENDSEN, YINMAN WANG, INGRID BAYER KRISTENSEN, HENRIK KJÆRULF JENSEN, JACOB TFELT-HANSEN and JYTTE BANNER

    Version of Record online : 6 AUG 2012, DOI: 10.1111/j.1540-8167.2012.02371.x

  14. Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

    Clinical Genetics

    Volume 70, Issue 3, September 2006, Pages: 214–227, G Millat, P Chevalier, L Restier-Miron, A Da Costa, P Bouvagnet, B Kugener, L Fayol, C Gonzàlez Armengod, B Oddou, V Chanavat, E Froidefond, R Perraudin, R Rousson and C Rodriguez-Lafrasse

    Version of Record online : 10 AUG 2006, DOI: 10.1111/j.1399-0004.2006.00671.x

  15. You have free access to this content
    Mutation of colocalized residues of the pore helix and transmembrane segments S5 and S6 disrupt deactivation and modify inactivation of KCNQ1 K+ channels

    The Journal of Physiology

    Volume 563, Issue 2, March 2005, Pages: 359–368, Guiscard Seebohm, Peter Westenskow, Florian Lang and Michael C. Sanguinetti

    Version of Record online : 21 FEB 2005, DOI: 10.1113/jphysiol.2004.080887

  16. Clinical Course and Risk Stratification of Patients Affected with the Jervell and Lange-Nielsen Syndrome

    Journal of Cardiovascular Electrophysiology

    Volume 17, Issue 11, November 2006, Pages: 1161–1168, ILAN GOLDENBERG, ARTHUR J. MOSS, WOJCIECH ZAREBA, SCOTT MCNITT, JENNIFER L. ROBINSON, MING QI, JEFFREY A. TOWBIN, MICHAEL J. ACKERMAN and LAURA MURPHY

    Version of Record online : 14 AUG 2006, DOI: 10.1111/j.1540-8167.2006.00587.x

  17. You have free access to this content
    Case ascertainment and estimated incidence of drug-induced long-QT syndrome: study in Southwest France

    British Journal of Clinical Pharmacology

    Volume 66, Issue 3, September 2008, Pages: 386–395, Mariam Molokhia, Atul Pathak, Maryse Lapeyre-Mestre, Laetitia Caturla, Jean Louis Montastruc, L'Association Française des Centres Régionaux de Pharmacovigilance (CRPV) and Paul McKeigue

    Version of Record online : 29 MAY 2008, DOI: 10.1111/j.1365-2125.2008.03229.x

  18. A Novel Mutation in KCNQ1 Associated with a Potent Dominant Negative Effect as the Basis for the LQT1 Form of the Long QT Syndrome

    Journal of Cardiovascular Electrophysiology

    Volume 18, Issue 9, September 2007, Pages: 972–977, YOSHIYASU AIZAWA, KAZUO UEDA, FABIANA SCORNIK, JONATHAN M. CORDEIRO, YUESHENG WU, MAYURIKA DESAI, ALEJANDRA GUERCHICOFF, YASUTOSHI NAGATA, YOSHITO IESAKA, AKINORI KIMURA, MASAYASU HIRAOKA and CHARLES ANTZELEVITCH

    Version of Record online : 26 JUL 2007, DOI: 10.1111/j.1540-8167.2007.00889.x

  19. Predictive genetic testing for cardiovascular diseases: Impact on carrier children

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 24, 15 December 2008, Pages: 3136–3146, Tineke M. Meulenkamp, Aad Tibben, Eline D. Mollema, Irene M. van Langen, Albert Wiegman, Guido M. de Wert, Inez D. de Beaufort, Arthur A.M. Wilde and Ellen M.A. Smets

    Version of Record online : 14 NOV 2008, DOI: 10.1002/ajmg.a.32592

  20. Long-QT Syndrome and Therapy for Attention Deficit/Hyperactivity Disorder

    Journal of Cardiovascular Electrophysiology

    Volume 26, Issue 10, October 2015, Pages: 1039–1044, CLAIRE ZHANG, VALENTINA KUTYIFA, ARTHUR J. MOSS, SCOTT MCNITT, WOJCIECH ZAREBA and ELIZABETH S. KAUFMAN

    Version of Record online : 6 AUG 2015, DOI: 10.1111/jce.12739