Recent Publications on Jervell-Lange Nielsen Syndrome: |  |
| A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.
| 13th September, 2008
| Department of Cardiovascular Medicine, Kyoto University Graduate School of
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Congenital long QT syndrome.
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease...
Direct Link | 12th August, 2008
| Section of Cardiology, Department of Lung, Blood and Heart, University of
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| Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance.
| 8th August, 2008
| Department of Otolaryngology, Faculty Division Rikshospitalet, University
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Cochlear implantation in children with Jervell, Lange-Nielsen syndrome.
Jervell, Lange-Nielsen syndrome is a condition that causes profound...
Direct Link | 20th June, 2008
| Head and Neck Surgery Department, Iran University of Medical Sciences,
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Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
BACKGROUND: Long QT syndrome (LQTS) is a cardiac disorder characterized by...
Direct Link | 1st May, 2008
| Key Laboratory of Molecular Biophysics of Ministry of Education, College
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| [Jervell and Lange-Nielsen syndrome]
| 8th December, 2007
| Department of Cardiovascular and Respiratory Medicine, Shiga University of
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[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome]
Data on the Jervell and Lange-Nielsen syndrome (JLN), the long QT syndrome...
Direct Link | 20th October, 2007
| Service de cardiologie, Hopital Lariboisiere, 2, rue Ambroise-Pare, 75010
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| Jervell-Lange Nielsen syndrome in a family with the long QT syndrome (LQTS).
| 23rd February, 2007
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| [KCNQ 1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family]
| 23rd February, 2007
| Departamento de Electrocardiologia, Instituto Nacional de Cardiologia
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Computational model of vectorial potassium transport by cochlear marginal cells and vestibular dark cells.
Cochlear marginal cells and vestibular dark cells transport potassium into...
Direct Link | 21st February, 2007
| Department of Bioengineering, M. S. 142, Rice University, Houston, TX
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Skipping of Exon 1 in the KCNQ1 gene causes Jervell and Lange-Nielsen syndrome.
The Jervell and Lange-Nielsen syndrome (JLNS) is a rare autosomal...
Direct Link | 19th January, 2007
| Universitatsklinikum Heidelberg, Innere Medizin III, Im Neuenheimer Feld
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Risk-stratifying Jervell and Lange-Nielsen syndrome from clinical data.
The Jervell and Lange-Nielsen syndrome (JLNS) is a rare autosomal...
Direct Link | 5th January, 2007
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Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome.
INTRODUCTION: Data regarding risk factors and clinical course of patients...
Direct Link | 5th January, 2007
| Division of Cardiology, Department of Medicine, University of Rochester
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Functional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytes.
The KCNQ gene family comprises voltage-gated potassium channels expressed...
Direct Link | 27th September, 2006
| Department of Physiology, University of Tuebingen, Tuebingen, Germany.
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| Jervell-Lange Nielsen syndrome in a family with the long QT Syndrome (LQTS).
| 15th August, 2006
| Department of Cardiovascular and Thoracic Surgery, IPGMER & SSKM Hospital,
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