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Results 1 to 25 of 330

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The antipsychotic drug chlorpromazine inhibits HERG potassium channelsTHOMAS, Dierk; KEZHONG WU; KATHÖFER, Sven et al.British journal of pharmacology. 2003, Vol 139, Num 3, pp 567-574, issn 0007-1188, 8 p.Article

Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndromeSHIMIZU, W; OHE, T; KURITA, T et al.Journal of the American College of Cardiology. 1995, Vol 26, Num 5, pp 1299-1309, issn 0735-1097Article

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromesCHOI, Grace; KOPPLIN, Laura J; TESTER, David J et al.Circulation (New York, N.Y.). 2004, Vol 110, Num 15, pp 2119-2124, issn 0009-7322, 6 p.Article

Blockade of HERG potassium currents by fluvoxamine: incomplete attenuation by S6 mutations at F656 or Y652MILNES, James T; CROCIANI, Olivia; ARCANGELI, Annarosa et al.British journal of pharmacology. 2003, Vol 139, Num 5, pp 887-898, issn 0007-1188, 12 p.Article

Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome : a worldwide reportSCHWARTZ, P. J; LOCATI, E. H; MOSS, A. J et al.Circulation (New York, N.Y.). 1991, Vol 84, Num 2, pp 503-511, issn 0009-7322Article

Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical PracticeTESTER, David J; ACKERMAN, Michael J.Circulation (New York, N.Y.). 2011, Vol 123, Num 9, pp 1021-1037, issn 0009-7322, 17 p.Article

How to Perform and Interpret Provocative Testing for the Diagnosis of Brugada Syndrome, Long-QT Syndrome, and Catecholaminergic Polymorphic Ventricular TachycardiaOBEYESEKERE, Manoj N; KLEIN, George J; MODI, Simon et al.Circulation. Arrhythmia and electrophysiology. 2011, Vol 4, Num 6, pp 958-964, issn 1941-3149, 7 p.Article

Common genetic variation in KCNH2 is associated with QT interval duration : The framingham heart studyNEWTON-CHEH, Christopher; GUO, Chao-Yu; HIRSCHHORN, Joel N et al.Circulation (New York, N.Y.). 2007, Vol 116, Num 10, pp 1128-1136, issn 0009-7322, 9 p.Article

Mechanism of hERG K+ channel blockade by the fluoroquinolone antibiotic moxifloxacinALEXANDROU, Ari J; DUNCAN, Rona S; SULLIVAN, Anneli et al.British journal of pharmacology. 2006, Vol 147, Num 8, pp 905-916, issn 0007-1188, 12 p.Article

Sudden unexplained death : Heritability and diagnostic yield of cardiological and genetic examination in surviving relativesTAN, Hanno L; HOFMAN, Nynke; VAN LANGEN, Irene M et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 2, pp 207-213, issn 0009-7322, 7 p.Article

Compound mutations: A common cause of severe long-Qt syndromeWESTENSKOW, Peter; SPLAWSKI, Igor; TIMOTHY, Katherine W et al.Circulation (New York, N.Y.). 2004, Vol 109, Num 15, pp 1834-1841, issn 0009-7322, 8 p.Article

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndromeSCHWARTZ, Peter J; PRIORI, Silvia G; ZAREBA, Wojciech et al.Circulation (New York, N.Y.). 2004, Vol 109, Num 15, pp 1826-1833, issn 0009-7322, 8 p.Article

Stillbirths, sudden infant deaths, and long-QT syndrome : Puzzle or mosaic, the pieces of the jigsaw are being fitted togetherSCHWARTZ, Peter J.Circulation (New York, N.Y.). 2004, Vol 109, Num 24, pp 2930-2932, issn 0009-7322, 3 p.Article

Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mrna decay in human long-QT syndromeQIUMING GONG; LI ZHANG; VINCENT, G. Michael et al.Circulation (New York, N.Y.). 2007, Vol 116, Num 1, pp 17-24, issn 0009-7322, 8 p.Article

Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanismANDERSON, Corey L; DELISLE, Brian P; ANSON, Blake D et al.Circulation (New York, N.Y.). 2006, Vol 113, Num 3, pp 365-373, issn 0009-7322, 9 p.Article

Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndromePARK, Kyu-Ho; PIRON, Julien; DAHIMENE, Shehrazade et al.Circulation research. 2005, Vol 96, Num 7, pp 730-739, issn 0009-7330, 10 p.Article

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndromeCROTTI, Lia; LUNDQUIST, Andrew L; SCHWARTZ, Peter J et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 9, pp 1251-1258, issn 0009-7322, 8 p.Article

New mechanism contributing to drug-induced arrhythmia : Rescue of a misprocessed LQT3 mutantKAI LIU; TAO YANG; VISWANATHAN, Prakash C et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 21, pp 3239-3246, issn 0009-7322, 8 p.Article

Non-equilibrium gating in cardiac Na+ channels: An original mechanism of arrhythmiaCLANCY, Colleen E; TATEYAMA, Michihiro; HUAJUN LIU et al.Circulation (New York, N.Y.). 2003, Vol 107, Num 17, pp 2233-2237, issn 0009-7322, 5 p.Article

Fetal Heart Rate Predictors of Long QT SyndromeMITCHELL, Jason L; CUNEO, Bettina F; ETHERIDGE, Susan P et al.Circulation (New York, N.Y.). 2012, Vol 126, Num 23, pp 2688-2695, issn 0009-7322, 8 p.Article

A Dual Mechanism for IKS Current Reduction by the Pathogenic Mutation KCNQ1-S277LCHEN, Jerri; WEBER, Michael; YON UM, Sung et al.Pacing and clinical electrophysiology. 2011, Vol 34, Num 12, pp 1652-1664, issn 0147-8389, 13 p.Article

Transmural Differences in Myocardial Contraction in Long-QT Syndrome: Mechanical Consequences of Ion Channel DysfunctionHAUGAA, Kristina Hermann; AMLIE, Jan P; BERGE, Knut Erik et al.Circulation (New York, N.Y.). 2010, Vol 122, Num 14, pp 1355-1363, issn 0009-7322, 9 p.Article

Long-QT Syndrome After Age 40GOLDENBERG, Ilan; MOSS, Arthur J; BENHORIN, Jesaia et al.Circulation (New York, N.Y.). 2008, Vol 117, Num 17, pp 2192-2201, issn 0009-7322, 10 p.Article

Sudden cardiac death in nephrology : focus on acquired long QT syndromeGUSSAK, Ihor; GUSSAK, Hiie M.Nephrology, dialysis, transplantation (Print). 2007, Vol 22, Num 1, pp 12-14, issn 0931-0509, 3 p.Article

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 geneMOSS, Arthur J; SHIMIZU, Wataru; HOFMAN, Nynke et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 19, pp 2481-2489, issn 0009-7322, 9 p.Article

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