UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2

Journal of the American College of Cardiology, 2012-11, Vol.60 (20), p.2092-2099

2012

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)

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Journal of the American College of Cardiology, 2012-11, Vol.60 (20), p.2092-2099

2012

Volltextzugriff (PDF)

Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade

Circulation (New York, N.Y.), 2022-11, Vol.146 (21), p.1610-1626

2022

Volltextzugriff (PDF)

Clinical utility gene card for: Long-QT syndrome

European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1825-1832

2021

Volltextzugriff (PDF)

Variant interpretation in molecular autopsy: a useful dilemma

International journal of legal medicine, 2022-03, Vol.136 (2), p.475-482

2022

Volltextzugriff (PDF)

Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony

Europace (London, England), 2014-12, Vol.16 (12), p.1752-1758

2014

Volltextzugriff (PDF)

Torsades de Pointes: A Rare Complication of an Extra-Adrenal Pheochromocytoma

Hypertension research, 2007-12, Vol.30 (12), p.1263-1266

2007

Volltextzugriff (PDF)

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Circulation. Cardiovascular genetics, 2015-06, Vol.8 (3), p.447-456

2015

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, 2013-11, Vol.45 (11), p.1409-1409

2013

Volltextzugriff (PDF)

Baseline Values and Sotalol-Induced Changes of Ventricular Repolarization Duration, Heterogeneity, and Instability in Patients With a History of Drug-Induced Torsades de Pointes

Journal of clinical pharmacology, 2009-01, Vol.49 (1), p.6-16

2009

Volltextzugriff (PDF)

Dual Inheritance of Sudden Death from Cardiovascular Causes

The New England journal of medicine, 2008-05, Vol.358 (19), p.2077-2078

2008

Volltextzugriff (PDF)

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study

European heart journal, 2007-02, Vol.28 (3), p.305-309

2007

Volltextzugriff (PDF)

Common variants in KCNN3 are associated with lone atrial fibrillation

Nature Genetics, 2010-03, Vol.42 (3), p.240-244

2010

Volltextzugriff (PDF)

Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure

The American journal of cardiology, 2010-07, Vol.106 (2), p.216-220

2010

Volltextzugriff (PDF)

Relation of Increased Short-Term Variability of QT Interval to Congenital Long-QT Syndrome

The American journal of cardiology, 2009-05, Vol.103 (9), p.1244-1248

2009

Volltextzugriff (PDF)

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

Nature genetics, 2013-11, Vol.45 (11), p.1409

2013

Volltextzugriff (PDF)

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

Nature genetics, 2013-10, Vol.45 (11), p.1409-1409

2013

Volltextzugriff (PDF)

Seizures on hearing the alarm clock

The Lancet (British edition), 2007-12, Vol.370 (9605), p.2172-2172

2007

Volltextzugriff (PDF)

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

European heart journal, 2019-09, Vol.40 (35), p.2964-2975

2019

Volltextzugriff (PDF)

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Circulation (New York, N.Y.), 2013-03, Vol.127 (9), p.1009-1017

2013

Volltextzugriff (PDF)

Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study

European heart journal, 2008-01, Vol.29 (2), p.185-190

2008

Volltextzugriff (PDF)

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

European heart journal, 2007-03, Vol.28 (5), p.575-580

2007

Volltextzugriff (PDF)

1 – 25 von 40

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(39)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(40)

Sprache

Englisch
(40)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2

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

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade

Clinical utility gene card for: Long-QT syndrome

Variant interpretation in molecular autopsy: a useful dilemma

Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

Torsades de Pointes: A Rare Complication of an Extra-Adrenal Pheochromocytoma

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

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

Baseline Values and Sotalol-Induced Changes of Ventricular Repolarization Duration, Heterogeneity, and Instability in Patients With a History of Drug-Induced Torsades de Pointes

Dual Inheritance of Sudden Death from Cardiovascular Causes

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study

Common variants in KCNN3 are associated with lone atrial fibrillation

Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure

Relation of Increased Short-Term Variability of QT Interval to Congenital Long-QT Syndrome

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

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

Lack of replication in polymorphisms reported to be associated with atrial fibrillation

Seizures on hearing the alarm clock

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Suchergebnisse filtern