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Items: 1 to 20 of 197

1.
QT Adaptation and Intrinsic QT Variability in Congenital Long QT Syndrome
Srikanth Seethala, Prabhpreet Singh, Vladimir Shusterman, Margareth Ribe, Kristina H. Haugaa, Jan Němec
J Am Heart Assoc. 2015 Dec; 4(12): e002395. Published online 2015 Dec 16. doi: 10.1161/JAHA.115.002395
PMCID:
PMC4845278
AbstractArticlePDF–433K
2.
Risk of Syncope in Family Members Who Are Genotype Negative for a Family-Associated Long QT Syndrome Mutation
Alon Barsheshet, Arthur J. Moss, Scott McNitt, Slava Polonsky, Coeli M. Lopes, Wojciech Zareba, Jennifer L. Robinson, Michael J. Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Jeffrey A. Towbin, G. Michael Vincent, Ming Qi, Ilan Goldenberg
Circ Cardiovasc Genet. Author manuscript; available in PMC 2013 Jun 23.
Published in final edited form as: Circ Cardiovasc Genet. 2011 Oct; 4(5): 491–499. Published online 2011 Aug 10. doi: 10.1161/CIRCGENETICS.111.960179
PMCID:
PMC3690290
AbstractArticlePDF–704K
3.
Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)
Sebastian Fröhler, Moritz Kieslich, Claudia Langnick, Mirjam Feldkamp, Bernd Opgen-Rhein, Felix Berger, Joachim C Will, Wei Chen
BMC Med Genet. 2014; 15: 48. Published online 2014 Apr 29. doi: 10.1186/1471-2350-15-48
PMCID:
PMC4038115
AbstractArticlePDF–464K
4.
Kcnq1-5 (Kv7.1-5) potassium channel expression in the adult zebrafish
Calvin Wu, Kanishk Sharma, Kyle Laster, Mohamed Hersi, Christina Torres, Thomas J Lukas, Ernest J Moore
BMC Physiol. 2014; 14: 1. Published online 2014 Feb 20. doi: 10.1186/1472-6793-14-1
PMCID:
PMC4016485
AbstractArticlePDF–2.2M
5.
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
Michael Christiansen, Paula L Hedley, Juliane Theilade, Birgitte Stoevring, Trond P Leren, Ole Eschen, Karina M Sørensen, Anne Tybjærg-Hansen, Lilian B Ousager, Lisbeth N Pedersen, Ruth Frikke-Schmidt, Frederik H Aidt, Michael G Hansen, Jim Hansen, Poul E Bloch Thomsen, Egon Toft, Finn L Henriksen, Henning Bundgaard, Henrik K Jensen, Jørgen K Kanters
BMC Med Genet. 2014; 15: 31. Published online 2014 Mar 7. doi: 10.1186/1471-2350-15-31
PMCID:
PMC4007532
AbstractArticlePDF–344K
6.
β-Blocker Efficacy in High-Risk Patients with the Congenital Long-QT Syndrome Types 1 and 2: Implications for Patient Management
Ilan Goldenberg, James Bradley, Arthur Moss, Scott McNitt, Slava Polonsky, Jennifer L. Robinson, Mark Andrews, Wojciech Zareba
J Cardiovasc Electrophysiol. Author manuscript; available in PMC 2014 Apr 30.
Published in final edited form as: J Cardiovasc Electrophysiol. 2010 Aug 1; 21(8): 893–901. Published online 2010 Mar 5. doi: 10.1111/j.1540-8167.2010.01737.x
PMCID:
PMC4005824
AbstractArticlePDF–958K
7.
Risk Factors for Aborted Cardiac Arrest and Sudden Cardiac Death in Children with the Congenital Long-QT Syndrome
Ilan Goldenberg, Arthur J. Moss, Derick R. Peterson, Scott McNitt, Wojciech Zareba, Mark L. Andrews, Jennifer L. Robinson, Emanuela H. Locati, Michael J. Ackerman, Jesaia Benhorin, Elizabeth S. Kaufman, Carlo Napolitano, Silvia G. Priori, Ming Qi, Peter J. Schwartz, Jeffrey A. Towbin, G. Michael Vincent, Li Zhang
Circulation. Author manuscript; available in PMC 2014 Mar 6.
Published in final edited form as: Circulation. 2008 Apr 29; 117(17): 2184–2191. Published online 2008 Apr 21. doi: 10.1161/CIRCULATIONAHA.107.701243
PMCID:
PMC3944375
AbstractArticlePDF–409K
8.
Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families
Annika Winbo, Eva-Lena Stattin, Charlotte Nordin, Ulla-Britt Diamant, Johan Persson, Steen M Jensen, Annika Rydberg
BMC Cardiovasc Disord. 2014; 14: 22. Published online 2014 Feb 19. doi: 10.1186/1471-2261-14-22
PMCID:
PMC3942207
AbstractArticlePDF–1.0M
9.
Genotype- and Phenotype-Guided Management of Congenital Long QT Syndrome
John R. Giudicessi, Michael J. Ackerman
Curr Probl Cardiol. Author manuscript; available in PMC 2014 Oct 1.
Published in final edited form as: Curr Probl Cardiol. 2013 Oct; 38(10): 417–455. doi: 10.1016/j.cpcardiol.2013.08.001
PMCID:
PMC3940076
AbstractArticlePDF–2.4M
10.
Calmodulin Mutations Associated with Recurrent Cardiac Arrest in Infants
Lia Crotti, Christopher N. Johnson, Elisabeth Graf, Gaetano M. De Ferrari, Bettina F. Cuneo, Marc Ovadia, John Papagiannis, Michael D. Feldkamp, Subodh G. Rathi, Jennifer D. Kunic, Matteo Pedrazzini, Thomas Wieland, Peter Lichtner, Britt-Maria Beckmann, Travis Clark, Christian Shaffer, D. Woodrow Benson, Stefan Kääb, Thomas Meitinger, Tim M. Strom, Walter J. Chazin, Peter J. Schwartz, Alfred L. George, Jr.
Circulation. Author manuscript; available in PMC 2014 Mar 5.
Published in final edited form as: Circulation. 2013 Mar 5; 127(9): 10.1161/CIRCULATIONAHA.112.001216. Published online 2013 Feb 6. doi: 10.1161/CIRCULATIONAHA.112.001216
PMCID:
PMC3834768
AbstractArticlePDF–2.9M
11.
Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels
Hai Huang, Silvia G. Priori, Carlo Napolitano, Michael E. O'Leary, Mohamed Chahine
Am J Physiol Heart Circ Physiol. 2011 Jan; 300(1): H288–H299. Published online 2010 Nov 12. doi: 10.1152/ajpheart.00539.2010
PMCID:
PMC3774256
AbstractArticle
12.
Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome
Nicole J. Boczek, Jabe M. Best, David J. Tester, John R. Giudicessi, Sumit Middha, Jared M. Evans, Timothy J. Kamp, Michael J. Ackerman
Circ Cardiovasc Genet. Author manuscript; available in PMC 2014 Jun 1.
Published in final edited form as: Circ Cardiovasc Genet. 2013 Jun; 6(3): 279–289. doi: 10.1161/CIRCGENETICS.113.000138
PMCID:
PMC3760222
AbstractArticlePDF–1.2M
13.
A COMMON VARIANT NEAR KCNJ2 GENE IS ASSOCIATED WITH T-PEAK TO T-END INTERVAL
Annukka Marjamaa, Lasse Oikarinen, Kimmo Porthan, Samuli Ripatti, Gina Peloso, Peter Noseworthy, Matti Viitasalo, Markku S. Nieminen, Lauri Toivonen, Kimmo Kontula, Leena Peltonen, Aki S. Havulinna, Antti Jula, Christopher J. O’Donnell, Christopher Newton-Cheh, Markus Perola, Veikko Salomaa
Heart Rhythm. Author manuscript; available in PMC 2013 Jul 1.
Published in final edited form as: Heart Rhythm. 2012 Jul; 9(7): 1099–1103. Published online 2012 Feb 15. doi: 10.1016/j.hrthm.2012.02.019
PMCID:
PMC3690340
AbstractArticlePDF–569K
14.
Nav1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link?
Pascal Gosselin-Badaroudine, Adrien Moreau, Mohamed Chahine
Channels (Austin) 2014 Jan 1; 8(1): 90–94. Published online 2013 Dec 3. doi: 10.4161/chan.27179
PMCID:
PMC4048347
AbstractArticlePDF–1.2M
15.
Prevalence and Potential Genetic Determinants of Sensorineural Deafness in KCNQ1 Homozygosity and Compound Heterozygosity
John R. Giudicessi, Michael J. Ackerman
Circ Cardiovasc Genet. Author manuscript; available in PMC 2014 Apr 1.
Published in final edited form as: Circ Cardiovasc Genet. 2013 Apr; 6(2): 193–200. Published online 2013 Feb 7. doi: 10.1161/CIRCGENETICS.112.964684
PMCID:
PMC3683572
AbstractArticlePDF–1.6M
16.
Single-channel basis for the slow activation of the repolarizing cardiac potassium current, IKs
Daniel Werry, Jodene Eldstrom, Zhuren Wang, David Fedida
Proc Natl Acad Sci U S A. 2013 Mar 12; 110(11): E996–E1005. Published online 2013 Feb 19. doi: 10.1073/pnas.1214875110
PMCID:
PMC3600500
AbstractArticlePDF–1.5M
17.
A Case of Long QT Syndrome Type 3 Aggravated by Beta-Blockers and Alleviated by Mexiletine: The Role of Epinephrine Provocation Test
Junbeom Park, Sook Kyoung Kim, Hui-Nam Pak
Yonsei Med J. 2013 Mar 1; 54(2): 529–533. Published online 2013 Jan 22. doi: 10.3349/ymj.2013.54.2.529
PMCID:
PMC3575977
AbstractArticlePDF–1.0M
18.
Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant
Lia Crotti, Dan Hu, Hector Barajas-Martinez, Gaetano M. De Ferrari, Antonio Oliva, Roberto Insolia, Guido D. Pollevick, Federica Dagradi, Alejandra Guerchicoff, Federica Greco, Peter J. Schwartz, Sami Viskin, Charles Antzelevitch
Heart Rhythm. Author manuscript; available in PMC 2013 Jul 1.
Published in final edited form as: Heart Rhythm. 2012 Jul; 9(7): 1104–1112. Published online 2012 Feb 13. doi: 10.1016/j.hrthm.2012.02.014
PMCID:
PMC3566559
AbstractArticlePDF–1.3M
19.
Left cardiac sympathetic denervation for the management of life-threatening ventricular tachyarrhythmias in young patients with catecholaminergic polymorphic ventricular tachycardia and long QT syndrome
Heike E. Schneider, Michael Steinmetz, Ulrich Krause, Thomas Kriebel, Wolfgang Ruschewski, Thomas Paul
Clin Res Cardiol. 2013; 102(1): 33–42. Published online 2012 Jul 21. doi: 10.1007/s00392-012-0492-7
PMCID:
PMC3536998
AbstractArticlePDF–427K
20.
PERTURBATION OF SODIUM CHANNEL STRUCTURE BY AN INHERITED LONG QT SYNDROME MUTATION
Ian W. Glaaser, Jeremiah D. Osteen, Akil Puckerin, Kevin J. Sampson, Xiangshu Jin, Robert S. Kass
Nat Commun. Author manuscript; available in PMC 2012 Dec 10.
Published in final edited form as: Nat Commun. 2012; 3: 706. Published online 2012 Feb 28. doi: 10.1038/ncomms1717
PMCID:
PMC3518026
AbstractArticlePDF–1.2M

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