نتایج جستجو برای: romano ward syndrome

تعداد نتایج: 645734  

2009
Po-Hsuan Hsu Yu-Chin Hsu Chung-Ming Kuan

Article history: Received 25 October 2008 Received in revised form 19 July 2009 Accepted 5 January 2010 Available online 18 January 2010 In the finance literature, statistical inferences for large-scale testing problems usually suffer from data snooping bias. In this paper we extend the “superior predictive ability” (SPA) test of Hansen (2005, JBES) to a stepwise SPA test that can identify pred...

Journal: :Circulation 2000
L Zhang K W Timothy G M Vincent M H Lehmann J Fox L C Giuli J Shen I Splawski S G Priori S J Compton F Yanowitz J Benhorin A J Moss P J Schwartz J L Robinson Q Wang W Zareba M T Keating J A Towbin C Napolitano A Medina

BACKGROUND Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding the slow component of the delayed rectifier current (LQT1, LQT5), the rapid component of the delayed rectifier current (LQT2, LQT6), or the Na(+) current (LQT3), resulting in ST-T-wave abnormalities on the ECG. This study evaluated the spectrum of ST-T-wave patterns and repolarization parameters by genotype a...

2015
Atefeh Mousavi Nik Somayeh Gharaie Hyo Jeong Kim

As a result of cell-specific functions of voltage-activated K(+) channels, such as Kv7.1, mutations in this channel produce profound cardiac and auditory defects. At the same time, the massive diversity of K(+) channels allows for compensatory substitution of mutant channels by other functional channels of their type to minimize defective phenotypes. Kv7.1 represents a clear example of such fun...

Journal: :Circulation 2001
J M Lupoglazoff I Denjoy M Berthet N Neyroud L Demay P Richard B Hainque G Vaksmann D Klug A Leenhardt G Maillard P Coumel P Guicheney

BACKGROUND The 2 genes KCNQ1 (LQT1) and HERG (LQT2), encoding cardiac potassium channels, are the most common cause of the dominant long-QT syndrome (LQTS). In addition to QT-interval prolongation, notched T waves have been proposed as a phenotypic marker of LQTS patients. METHODS AND RESULTS The T-wave morphology of carriers of mutations in KCNQ1 (n=133) or HERG (n=57) and of 100 control sub...

Journal: :Circulation 2011
Jonathan Buber Jehu Mathew Arthur J Moss W Jackson Hall Alon Barsheshet Scott McNitt Jennifer L Robinson Wojciech Zareba Michael J Ackerman Elizabeth S Kaufman David Luria Michael Eldar Jeffrey A Towbin Michael Vincent Ilan Goldenberg

BACKGROUND Women with congenital long-QT syndrome experience an increased risk for cardiac events after the onset of adolescence that is more pronounced among carriers of the LQT2 genotype. We hypothesized that the hormonal changes associated with menopause may affect clinical risk in this population. METHODS AND RESULTS We used a repeated-events analysis to evaluate the risk for recurrent sy...

2011
Petri Haapalahti Matti Viitasalo Merja Perhonen Heikki Väänänen Markku Mäkijärvi Heikki Swan Lauri Toivonen

BACKGROUND   LQT1 subtype of long QT syndrome is characterized by defective I(Ks) , which is intrinsically stronger in the epicardium than in the midmyocardial region. Electrocardiographic QT peak and QT end intervals may reflect complete repolarization of epicardium and midmyocardial region of the ventricular wall, respectively. Repolarization abnormalities in LQT1 carriers may therefore be mo...

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2004

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