Found: 31
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Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.
- Published in:
- EP: Europace, 2014, v. 16, n. 12, p. 1828, doi. 10.1093/europace/euu063
- By:
- Publication type:
- Article
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.
- Published in:
- EP: Europace, 2014, v. 16, n. 11, p. 1646, doi. 10.1093/europace/eut382
- By:
- Publication type:
- Article
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Triggering of high-speed neurite outgrowth using an optical microheater.
- Published in:
- Scientific Reports, 2015, p. 16611, doi. 10.1038/srep16611
- By:
- Publication type:
- Article
Population Pharmacokinetics and Pharmacodynamics of Apixaban Linking Its Plasma Concentration to Intrinsic Activated Coagulation Factor X Activity in Japanese Patients with Atrial Fibrillation.
- Published in:
- AAPS Journal, 2019, v. 21, n. 5, p. N.PAG, doi. 10.1208/s12248-019-0353-7
- By:
- Publication type:
- Article
Gain-of-Function KCNH2 Mutations in Patients with Brugada Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2014, v. 25, n. 5, p. 522, doi. 10.1111/jce.12361
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- Publication type:
- Article
Cardiac Channelopathies Associated with Infantile Fatal Ventricular Arrhythmias: From the Cradle to the Bench.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2014, v. 25, n. 1, p. 66, doi. 10.1111/jce.12270
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- Publication type:
- Article
Age- and Genotype-Specific Triggers for Life-Threatening Arrhythmia in the Genotyped Long QT Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2008, v. 19, n. 8, p. 794, doi. 10.1111/j.1540-8167.2008.01138.x
- By:
- Publication type:
- Article
A Novel Missense Mutation in theSCN5AGene Associated with Brugada Syndrome Bidirectionally Affecting Blocking Actions of Antiarrhythmic Drugs.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2005, v. 16, n. 5, p. 486, doi. 10.1111/j.1540-8167.2005.40711.x
- By:
- Publication type:
- Article
Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-Pore Site ofSCN5A.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2005, v. 16, n. 4, p. 378, doi. 10.1046/j.1540-8167.2005.40606.x
- By:
- Publication type:
- Article
Practical applicability of landiolol, an ultra-short-acting β1-selective blocker, for rapid atrial and ventricular tachyarrhythmias with left ventricular dysfunction.
- Published in:
- Journal of Arrhythmia, 2016, v. 32, n. 2, p. 82, doi. 10.1016/j.joa.2015.09.002
- By:
- Publication type:
- Article
A rare KCNE1 polymorphism, D85N, as a genetic modifier of long QT syndrome.
- Published in:
- Journal of Arrhythmia, 2014, v. 30, n. 3, p. 161, doi. 10.1016/j.joa.2013.08.004
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- Publication type:
- Article
Carvedilol, a Non-Selective β-with α1-Blocker is Effective in Long QT Syndrome Type 2
- Published in:
- Journal of Arrhythmia, 2011, v. 27, n. 4, p. 324, doi. 10.1016/S1880-4276(11)80034-7
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- Publication type:
- Article
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation.
- Published in:
- British Journal of Clinical Pharmacology, 2018, v. 84, n. 6, p. 1301, doi. 10.1111/bcp.13561
- By:
- Publication type:
- Article
Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-13363-3
- By:
- Publication type:
- Article
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents.
- Published in:
- Cardiovascular Research, 2012, v. 93, n. 4, p. 666, doi. 10.1093/cvr/cvr329
- By:
- Publication type:
- Article
Extracorporeal membrane oxygenation for the anesthetic management of a patient with severe airway stenosis caused by thyroid carcinoma invasion.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
A Clinical Trial Evaluating the Efficacy of Deep Learning-Based Facial Recognition for Patient Identification in Diverse Hospital Settings.
- Published in:
- Bioengineering (Basel), 2024, v. 11, n. 4, p. 384, doi. 10.3390/bioengineering11040384
- By:
- Publication type:
- Article
T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin i mutation than qt dispersion.
- Published in:
- Clinical Cardiology, 2002, v. 25, n. 7, p. 335, doi. 10.1002/clc.4950250706
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- Publication type:
- Article
Clinical Care Recommendations for Cardiologists Treating Adults With Myotonic Dystrophy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Novel KCNQ1 Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents.
- Published in:
- Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1401822
- By:
- Publication type:
- Article
Dynorphins directly inhibit neuronal nicotinic acetylcholine receptors in PC12 cells.
- Published in:
- European Journal of Neuroscience, 2000, v. 12, n. 4, p. 1253, doi. 10.1046/j.1460-9568.2000.00012.x
- By:
- Publication type:
- Article
Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164795
- By:
- Publication type:
- Article
A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG.
- Published in:
- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0161872
- By:
- Publication type:
- Article
Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome.
- Published in:
- PLoS ONE, 2022, v. 17, n. 7, p. 1, doi. 10.1371/journal.pone.0271796
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- Publication type:
- Article
The genetics underlying acquired long QT syndrome: impact for genetic screening.
- Published in:
- European Heart Journal, 2016, v. 37, n. 18, p. 1456, doi. 10.1093/eurheartj/ehv695
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- Publication type:
- Article
Low HDL cholesterol is associated with the risk of stroke in elderly diabetic individuals: changes in the risk for atherosclerotic diseases at various ages.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Low HDL Cholesterol Is Associated With the Risk of Stroke in Elderly Diabetic Individuals.
- Published in:
- Diabetes Care, 2009, v. 32, n. 7, p. 1221, doi. 10.2337/dc08-1677
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- Publication type:
- Article
Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome.
- Published in:
- EP: Europace, 2010, v. 12, n. 11, p. 1623, doi. 10.1093/europace/euq342
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- Publication type:
- Article
Prognostic Value of DNA Ploidy Patterns of Colorectal Adenocarcinoma: Univariate and Multivariate Analysis.
- Published in:
- Digestive Surgery, 1998, v. 15, n. 6, p. 687, doi. 10.1159/000018679
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- Publication type:
- Article