Found: 156
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J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
- Published in:
- 2017
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- Publication type:
- journal article
Quantitative analysis of PKP2 and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygous PKP2 deletion.
- Published in:
- 2017
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- Publication type:
- journal article
Novel SCN10A variants associated with Brugada syndrome.
- Published in:
- 2016
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- Publication type:
- journal article
Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case report.
- Published in:
- 2017
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- Publication type:
- journal article
Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome.
- Published in:
- EP: Europace, 2023, v. 25, n. 4, p. 1491, doi. 10.1093/europace/euac269
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- Publication type:
- Article
School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome.
- Published in:
- 2022
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- Publication type:
- journal article
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome.
- Published in:
- 2022
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- Publication type:
- journal article
Different responses to exercise between Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- 2018
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- 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
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- Publication type:
- Article
Author reply.
- Published in:
- EP: Europace, 2014, v. 16, n. 12, p. 1864, doi. 10.1093/europace/euu061
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- 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
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- Publication type:
- Article
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
- Published in:
- 2013
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- Publication type:
- Journal Article
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
- Published in:
- EP: Europace, 2013, v. 15, n. 10, p. 1389
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- Publication type:
- Article
Open channel block of Kv1.5 channels by HMQ1611.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.965086
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- Publication type:
- Article
Augmentation Index and Pulse Wave Velocity as Indicators of Cardiovascular Stiffness.
- Published in:
- Angiology, 2008, v. 59, n. 4, p. 421, doi. 10.1177/0003319707306299
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- Publication type:
- Article
NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function.
- Published in:
- EMBO Journal, 2003, v. 22, n. 23, p. 6310, doi. 10.1093/emboj/cdg601
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- Publication type:
- Article
Late presentation of arrhythmogenic right ventricular cardiomyopathy in an octogenarian associated with a pathogenic variant in the plakophilin 2 gene: a case report.
- Published in:
- 2019
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- Publication type:
- Case Study
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
- Published in:
- 2008
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- Publication type:
- journal article
Cardiac Chloride Channels: Incremental Regulation by Phosphorylation/Dephosphorylation<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1993, v. 707, n. 1, p. 259, doi. 10.1111/j.1749-6632.1993.tb38057.x
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- Publication type:
- Article
Characterization of the rapidly activating delayed rectifier potassium current, I (Kr), in HL-1 mouse atrial myocytes.
- Published in:
- 2010
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- Publication type:
- journal article
Cytoplasmic terminus domains of Kir6.x confer different nucleotide-dependent gating on the ATP-sensitive K<sup>+</sup> channel.
- Published in:
- Journal of Physiology, 1998, v. 512, n. 2, p. 395, doi. 10.1111/j.1469-7793.1998.395be.x
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- Publication type:
- Article
Long QT syndrome with a de novo CALM2 mutation in a 4‐year‐old boy.
- Published in:
- Pediatrics International, 2019, v. 61, n. 9, p. 852, doi. 10.1111/ped.13959
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- Publication type:
- Article
Catecholaminergic polymorphic ventricular tachycardia managed as orthostatic dysregulation and epilepsy in 11‐ and 15‐year‐old sisters.
- Published in:
- Pediatrics International, 2018, v. 60, n. 11, p. 998, doi. 10.1111/ped.13688
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- Publication type:
- Article
Increased Ca<sub>V</sub>1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-23512-2
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- Publication type:
- Article
Assessment of disease-associated missense variants in RYR2 on transcript splicing.
- Published in:
- Cardiogenetics, 2020, v. 10, n. 1, p. 11, doi. 10.4081/cardiogenetics.2020.8637
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- Publication type:
- Article
Evaluation and management of bradycardia in neonates and children.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Erratum to "Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients".
- Published in:
- Stem Cells International, 2020, p. 1, doi. 10.1155/2020/8765895
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- Publication type:
- Article
Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients.
- Published in:
- Stem Cells International, 2019, p. 1, doi. 10.1155/2019/7532657
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- Publication type:
- Article
Cardiomyopathy with an LMNA Genetic Variant Affecting Three Consecutive Generations: A Case Series.
- Published in:
- Internal Medicine, 2024, v. 63, n. 18, p. 2533, doi. 10.2169/internalmedicine.1701-23
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- Publication type:
- Article
Successful Management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator.
- Published in:
- Internal Medicine, 2022, v. 61, n. 8, p. 1179, doi. 10.2169/internalmedicine.8093-21
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- Publication type:
- Article
Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose.
- Published in:
- 2020
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- Publication type:
- Case Study
Association between brachial-ankle pulse wave velocity and endothelium-dependent and -independent coronary vasomotor function.
- Published in:
- Clinical & Experimental Pharmacology & Physiology, 2011, v. 38, n. 1, p. 34, doi. 10.1111/j.1440-1681.2010.05455.x
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- 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
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- Publication type:
- Article
Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0131517
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- Publication type:
- Article
QT Is Longer in Drug-Free Patients with Schizophrenia Compared with Age-Matched Healthy Subjects.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0098555
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- Publication type:
- Article
Pandora will never regret having opened her box: reappraisal of genes associated with CPVT and SQTS.
- Published in:
- European Heart Journal, 2022, v. 43, n. 15, p. 1511, doi. 10.1093/eurheartj/ehab794
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- Publication type:
- Article
Clinical and neurophysiological variability in Andersen-Tawil syndrome.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Angiotensin-converting enzyme inhibition and fibrinolytic balance.
- Published in:
- Hypertension Research, 2011, v. 34, n. 4, p. 448, doi. 10.1038/hr.2011.3
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- Publication type:
- Article
Comparison of the long-term effects of candesartan and olmesartan on plasma angiotensin II and left ventricular mass index in patients with hypertension.
- Published in:
- Hypertension Research, 2010, v. 33, n. 2, p. 118, doi. 10.1038/hr.2009.192
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- Publication type:
- Article
Long-term effect of efonidipine therapy on plasma aldosterone and left ventricular mass index in patients with essential hypertension.
- Published in:
- Hypertension Research, 2009, v. 32, n. 8, p. 670, doi. 10.1038/hr.2009.78
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- Publication type:
- Article
Comparison of the Effects of Efonidipine and Amlodipine on Aldosterone in Patients with Hypertension.
- Published in:
- Hypertension Research, 2007, v. 30, n. 8, p. 691, doi. 10.1291/hypres.30.691
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- Publication type:
- Article
Relationship between Metabolic Syndrome and Trp64Arg Polymorphism of the β3-Adrenergic Receptor Gene in a General Sample: The Shigaraki Study.
- Published in:
- Hypertension Research, 2006, v. 29, n. 11, p. 891, doi. 10.1291/hypres.29.891
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- Publication type:
- Article
The Association between Morning Hypertension and Metabolic Syndrome in Hypertensive Patients.
- Published in:
- Hypertension Research, 2006, v. 29, n. 10, p. 783, doi. 10.1291/hypres.29.783
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- Publication type:
- Article
Impact of Paraoxonase Polymorphism (Q192R) on Endothelial Function in Intact Coronary Circulation.
- Published in:
- Hypertension Research, 2006, v. 29, n. 6, p. 417, doi. 10.1291/hypres.29.417
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- Publication type:
- Article
Combined Analysis of Polymorphisms in Angiotensinogen and Adducin Genes and Their Effects on Hypertension in a Japanese Sample: The Shigaraki Study.
- Published in:
- Hypertension Research, 2005, v. 28, n. 8, p. 645, doi. 10.1291/hypres.28.645
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- Publication type:
- Article
Brachial Artery Flow-Mediated Vasodilation Is Correlated with Coronary Vasomotor and Fibrinolytic Responses Induced by Bradykinin.
- Published in:
- Hypertension Research, 2005, v. 28, n. 1, p. 59, doi. 10.1291/hypres.28.59
- By:
- Publication type:
- Article
Arrhythmogenic right-ventricular cardiomyopathy with plakophilin-2 genetic variant concomitant with early manifestation of ventricular tachyarrhythmia: a case series.
- Published in:
- European Heart Journal Case Reports, 2022, v. 6, n. 10, p. 1, doi. 10.1093/ehjcr/ytac397
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- 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
Time Course and Prognostic Implications of QT Interval in Patients with Coronary Artery Disease Undergoing Coronary Bypass Surgery.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2012, v. 23, n. 6, p. 645, doi. 10.1111/j.1540-8167.2011.02244.x
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- Publication type:
- Article