UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 55

Sortiert nach

An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Heart rhythm, 2010-01, Vol.7 (1), p.33-46

2010

Volltextzugriff (PDF)

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Genetics in medicine, 2021-01, Vol.23 (1), p.47-58

2021

Volltextzugriff (PDF)

A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction

Circulation research, 2017-05, Vol.120 (10), p.e33-e44

2017

Volltextzugriff (PDF)

Corneal Densitometry as a Novel Technique for Monitoring Amiodarone Therapy

Ophthalmology (Rochester, Minn.), 2016-11, Vol.123 (11), p.2294-2299

2016

Volltextzugriff (PDF)

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

European heart journal, 2016-02, Vol.37 (7), p.640-650

2016

Volltextzugriff (PDF)

Sodium permeable and “hypersensitive” TREK ‐1 channels cause ventricular tachycardia

EMBO molecular medicine, 2017-04, Vol.9 (4), p.403-414

2017

Volltextzugriff (PDF)

Gain‐of‐function mutation in TASK‐4 channels and severe cardiac conduction disorder

EMBO molecular medicine, 2014-07, Vol.6 (7), p.937-951

2014

Volltextzugriff (PDF)

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

European journal of human genetics : EJHG, 2016-08, Vol.24 (8), p.1160-1166

2016

Volltextzugriff (PDF)

Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K + Channel) Channel Function

Circulation. Genomic and precision medicine, 2019-01, Vol.12 (1), p.e002238-e002238

2019

Volltextzugriff (PDF)

Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs

PloS one, 2016-07, Vol.11 (7), p.e0158085-e0158085

2016

Volltextzugriff (PDF)

A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

PloS one, 2013-06, Vol.8 (6), p.e67963

2013

Volltextzugriff (PDF)

Intraoperative Defibrillation Testing of Subcutaneous Implantable Cardioverter‐Defibrillator Systems—A Simple Issue?

Journal of the American Heart Association, 2016-03, Vol.5 (3), p.e003181-n/a

2016

Volltextzugriff (PDF)

High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature

Journal of cardiology cases, 2015-01, Vol.11 (1), p.10-13

2015

Volltextzugriff (PDF)

T peak –T end interval and T peak –T end /QT ratio in patients with Brugada syndrome

Europace (London, England), 2016-12, p.euw033

2016

Volltextzugriff (PDF)

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Nature genetics, 2013-09, Vol.45 (9), p.1044-1049

2013

Volltextzugriff (PDF)

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Circulation (New York, N.Y.), 2020-07, Vol.142 (4), p.324-338

2020

Volltextzugriff (PDF)

Safety of Endomyocardial Biopsy in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy

JACC. Cardiovascular interventions, 2011-10, Vol.4 (10), p.1142-1148

2011

Volltextzugriff (PDF)

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome

Journal of molecular and cellular cardiology, 2015-03, Vol.80, p.186-195

2015

Volltextzugriff (PDF)

Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

Human mutation, 2012-01, Vol.33 (1), p.109-117

2012

Volltextzugriff (PDF)

(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply

Europace (London, England), 2017-04, Vol.19 (4), p.696-697

2017

Volltextzugriff (PDF)

Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

Human mutation, 2012-01, Vol.33 (1), p.109-117

2012

Volltextzugriff (PDF)

POPDC2 a novel susceptibility gene for conduction disorders

Journal of molecular and cellular cardiology, 2020-08, Vol.145, p.74-83

2020

Volltextzugriff (PDF)

Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia

EMBO molecular medicine, 2017-04, Vol.9 (4), p.403-414

2017

Volltextzugriff (PDF)

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

European heart journal, 2016-02, Vol.37 (7), p.640-650

2016

Volltextzugriff (PDF)

1 – 25 von 55

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(49)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Europace
(5)
Herz
(4)
Nature Genetics
(4)
Plos One
(4)
Embo Molecular Medicine
(3)
Genetics In Medicine
(3)
Human Mutation
(3)
Circulation
(2)
Circulation. Cardiovascular Genetics
(2)
Clinical Research In Cardiology
(2)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction

Corneal Densitometry as a Novel Technique for Monitoring Amiodarone Therapy

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

Sodium permeable and “hypersensitive” TREK ‐1 channels cause ventricular tachycardia

Gain‐of‐function mutation in TASK‐4 channels and severe cardiac conduction disorder

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K + Channel) Channel Function

Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs

A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

Intraoperative Defibrillation Testing of Subcutaneous Implantable Cardioverter‐Defibrillator Systems—A Simple Issue?

High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature

T peak –T end interval and T peak –T end /QT ratio in patients with Brugada syndrome

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Safety of Endomyocardial Biopsy in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome

Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply

Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

POPDC2 a novel susceptibility gene for conduction disorders

Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

Suchergebnisse filtern