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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 2
2011 1
2013 1
2014 1
2015 2
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2017 2
2019 1
2020 1
2022 1
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11 results

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Page 1
Identification of Low-Risk Adult Congenital LQTS Patients.
Zhang C, Kutyifa V, McNitt S, Zareba W, Goldenberg I, Moss AJ. Zhang C, et al. J Cardiovasc Electrophysiol. 2015 Aug;26(8):853-858. doi: 10.1111/jce.12686. Epub 2015 May 28. J Cardiovasc Electrophysiol. 2015. PMID: 25872798
Detecting Underlying Cardiovascular Disease in Young Competitive Athletes.
McKinney J, Lithwick DJ, Morrison BN, Nazzari H, Luong M, Fordyce CB, Taunton J, Krahn AD, Heilbron B, Isserow S. McKinney J, et al. Can J Cardiol. 2017 Jan;33(1):155-161. doi: 10.1016/j.cjca.2016.06.007. Epub 2016 Jun 23. Can J Cardiol. 2017. PMID: 27692657
RESULTS: Overall, 7 YCAs (0.52%) were found to have clinically significant diagnoses associated with SCD (4 pre-excitation, 1 long QT syndrome, 1 mitral valve prolapse, 1 hypertrophic cardiomyopathy). ...
RESULTS: Overall, 7 YCAs (0.52%) were found to have clinically significant diagnoses associated with SCD (4 pre-excitation, 1 long …
Separation of HCM and LQT Cardiac Diseases with Machine Learning of Ca2+ Transient Profiles.
Joutsijoki H, Penttinen K, Juhola M, Aalto-Setälä K. Joutsijoki H, et al. Methods Inf Med. 2019 Nov;58(4-05):167-178. doi: 10.1055/s-0040-1701484. Epub 2020 Feb 20. Methods Inf Med. 2019. PMID: 32079026
., TPM1 (HCMT) or MYBPC3 or myosin-binding protein C (HCMM) mutation and LQTS signals included data recorded from iPSC-CMs carrying potassium voltage-gated channel subfamily Q member 1 (KCNQ1) mutation (long QT syndrome 1 [LQT1]) or KCNH2 mutation (lon …
., TPM1 (HCMT) or MYBPC3 or myosin-binding protein C (HCMM) mutation and LQTS signals included data recorded from iPSC-CMs carrying potassiu …
Nicorandil normalizes prolonged repolarisation in the first transgenic rabbit model with Long-QT syndrome 1 both in vitro and in vivo.
Biermann J, Wu K, Odening KE, Asbach S, Koren G, Peng X, Zehender M, Bode C, Brunner M. Biermann J, et al. Eur J Pharmacol. 2011 Jan 10;650(1):309-16. doi: 10.1016/j.ejphar.2010.10.016. Epub 2010 Oct 17. Eur J Pharmacol. 2011. PMID: 20959120 Free PMC article.
Transgenic rabbits expressing loss-of-function pore mutants of the human gene KCNQ1 (K(v)LQT1-Y315S) have a Long QT-Syndrome 1 (LQT1) phenotype. We evaluated for the first time the effect of nicorandil, an opener of ATP-sensitive potassium channels, an …
Transgenic rabbits expressing loss-of-function pore mutants of the human gene KCNQ1 (K(v)LQT1-Y315S) have a Long QT-Syndrom …
Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience.
Wong LC, Roses-Noguer F, Till JA, Behr ER. Wong LC, et al. Circ Arrhythm Electrophysiol. 2014 Oct;7(5):800-6. doi: 10.1161/CIRCEP.114.001818. Epub 2014 Sep 6. Circ Arrhythm Electrophysiol. 2014. PMID: 25194972
Genetic testing identified mutations in 20% of Brugada syndrome (2/10) and 50% of long QT syndrome (1/2) and catecholaminergic polymorphic ventricular tachycardia families (1/2) who were tested. ...
Genetic testing identified mutations in 20% of Brugada syndrome (2/10) and 50% of long QT syndrome (1/2) and cat …
4,4'-Diisothiocyanato-2,2'-Stilbenedisulfonic Acid (DIDS) Modulates the Activity of KCNQ1/KCNE1 Channels by an Interaction with the Central Pore Region.
Bollmann E, Schreiber JA, Ritter N, Peischard S, Ho HT, Wünsch B, Strünker T, Meuth S, Budde T, Strutz-Seebohm N, Seebohm G. Bollmann E, et al. Cell Physiol Biochem. 2020 Apr 8;54(2):321-332. doi: 10.33594/000000222. Cell Physiol Biochem. 2020. PMID: 32259418 Free article.
Genetic aberrations that affect the activity of KCNQ1/KCNE1 can lead to the Long QT Syndrome 1 and 5 and, thereby, to a predisposition to sudden cardiac death. ...
Genetic aberrations that affect the activity of KCNQ1/KCNE1 can lead to the Long QT Syndrome 1 and 5 and, thereb …
Low Prevalence of Inappropriate Shocks in Patients With Inherited Arrhythmia Syndromes With the Subcutaneous Implantable Defibrillator Single Center Experience and Long-Term Follow-Up.
Rudic B, Tülümen E, Berlin V, Röger S, Stach K, Liebe V, El-Battrawy I, Dösch C, Papavassiliu T, Akin I, Borggrefe M, Kuschyk J. Rudic B, et al. J Am Heart Assoc. 2017 Oct 17;6(10):e006265. doi: 10.1161/JAHA.117.006265. J Am Heart Assoc. 2017. PMID: 29042423 Free PMC article.
The study cohort comprised of 24 patients with Brugada syndrome, 17 with idiopathic ventricular fibrillation, 6 with long-QT syndrome, 1 with short-QT syndrome, 3 with catecholaminergic polymorphic ventricular tachycardia, 8 with hypertrophic cardiomyo …
The study cohort comprised of 24 patients with Brugada syndrome, 17 with idiopathic ventricular fibrillation, 6 with long-QT …
11 results