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...

Desmosomes and the sodium channel complex: Implications for arrhythmogenic cardiomyopathy and Brugada syndrome

Trends in cardiovascular medicine, 2014-07, Vol.24 (5), p.184-190

2014

Volltextzugriff (PDF)

Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy

Journal of the American Heart Association, 2018-06, Vol.7 (12)

Cerrone, Marina

2018

Volltextzugriff (PDF)

Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency

Cardiovascular research, 2012-09, Vol.95 (4), p.460-468

2012

Volltextzugriff (PDF)

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

Proceedings of the National Academy of Sciences - PNAS, 2013-03, Vol.110 (11), p.4291-4296

2013

Volltextzugriff (PDF)

Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias

The Journal of clinical investigation, 2015-01, Vol.125 (1), p.403-412

2015

Volltextzugriff (PDF)

Ca2+ dysregulation in cardiac stromal cells sustains fibro-adipose remodeling in Arrhythmogenic Cardiomyopathy and can be modulated by flecainide

Journal of translational medicine, 2022-11, Vol.20 (1), p.1-20, Article 522

2022

Volltextzugriff (PDF)

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca2+ regulation

Heart rhythm, 2009-11, Vol.6 (11), p.1652-1659

2009

Volltextzugriff (PDF)

Editorial commentary: Non-invasive tools for risk stratification and treatment in Brugada syndrome: Less is more?

Trends in cardiovascular medicine, 2021-07, Vol.31 (5), p.330-331

Cerrone, Marina

2021

Volltextzugriff (PDF)

Connexin43 contributes to electrotonic conduction across scar tissue in the intact heart

Scientific reports, 2016-05, Vol.6 (1), p.26744-26744, Article 26744

2016

Volltextzugriff (PDF)

Pleiotropic Phenotypes Associated With PKP2 Variants

Frontiers in cardiovascular medicine, 2018-12, Vol.5, p.184-184

2018

Volltextzugriff (PDF)

Arrhythmogenic Mechanisms in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation research, 2007-11, Vol.101 (10), p.1039-1048

2007

Volltextzugriff (PDF)

Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor

Circulation research, 2005-05, Vol.96 (10), p.e77-e82

2005

Volltextzugriff (PDF)

Performance of a Protein Language Model for Variant Annotation in Cardiac Disease

Journal of the American Heart Association, 2024-10, Vol.13 (20), p.e036921

2024

Volltextzugriff (PDF)

Controversies in Brugada syndrome

Trends in cardiovascular medicine, 2018-05, Vol.28 (4), p.284-292

Cerrone, Marina

2018

Volltextzugriff (PDF)

Transcriptomic Coupling of PKP2 With Inflammatory and Immune Pathways Endogenous to Adult Cardiac Myocytes

Frontiers in physiology, 2021-01, Vol.11, p.623190-623190

2021

Volltextzugriff (PDF)

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

Circulation (New York, N.Y.), 2004-04, Vol.109 (15), p.1826-1833

2004

Volltextzugriff (PDF)

Risk indicators in long QT syndrome: Does location matter?

Heart rhythm, 2012-06, Vol.9 (6), p.899-900

Cerrone, Marina, MD

2012

Volltextzugriff (PDF)

Up-regulation of the inward rectifier K+ current (IK1) in the mouse heart accelerates and stabilizes rotors

The Journal of physiology, 2007-01, Vol.578 (1), p.315-326

2007

Volltextzugriff (PDF)

Blockade of the Adenosine 2A Receptor Mitigates the Cardiomyopathy Induced by Loss of Plakophilin-2 Expression

Frontiers in physiology, 2018-12, Vol.9, p.1750-1750

2018

Volltextzugriff (PDF)

Management of Congenital Long-QT Syndrome: Commentary From the Experts

Circulation. Arrhythmia and electrophysiology, 2021-07, Vol.14 (7), p.e009726-e009726

2021

Volltextzugriff (PDF)

Arrhythmogenic cardiomyopathy and Brugada syndrome: Diseases of the connexome

FEBS letters, 2014-04, Vol.588 (8), p.1322-1330

2014

Volltextzugriff (PDF)

The Genetics of Brugada Syndrome

Annual review of genomics and human genetics, 2022-08, Vol.23 (1), p.255-274

2022

Volltextzugriff (PDF)

Discerning From the Good, the Bad, and the Ugly

Circulation. Arrhythmia and electrophysiology, 2017-04, Vol.10 (4), p.e005209-e005209

Cerrone, Marina

2017

Volltextzugriff (PDF)

ICD shocks and complications in patients with inherited arrhythmia syndromes

International journal of cardiology. Heart & vasculature, 2021-12, Vol.37, p.100908, Article 100908

2021

Volltextzugriff (PDF)

Sudden Cardiac Arrest in a Patient With Mitral Valve Prolapse and LMNA and SCN5A Mutations

JACC. Case reports, 2021-02, Vol.3 (2), p.242-246

2021

Volltextzugriff (PDF)

1 – 25 von 109

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(93)
Mit Volltextzugriff
(91)

Publikationsform

Sprache

Englisch
(108)
Italienisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(60)
Life Sciences & Biomedicine
(55)
Humans
(43)
Cardiac & Cardiovascular Systems
(41)
Cardiovascular System & Cardiology
(41)
Animals
(19)
Mutation
(17)
Electrocardiography
(14)
Male
(13)
Mice
(13)
Genetics
(12)
Phenotype
(12)
Plakophilins - Genetics
(12)
Cardiomyopathy
(11)
Female
(11)
Adult
(10)
Arrhythmias, Cardiac - Genetics
(10)
Arrhythmogenic Right Ventricular Dysplasia - Genetics
(9)
Brugada Syndrome
(9)
Cardiovascular
(9)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Desmosomes and the sodium channel complex: Implications for arrhythmogenic cardiomyopathy and Brugada syndrome

Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy

Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias

Ca2+ dysregulation in cardiac stromal cells sustains fibro-adipose remodeling in Arrhythmogenic Cardiomyopathy and can be modulated by flecainide

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca2+ regulation

Editorial commentary: Non-invasive tools for risk stratification and treatment in Brugada syndrome: Less is more?

Connexin43 contributes to electrotonic conduction across scar tissue in the intact heart

Pleiotropic Phenotypes Associated With PKP2 Variants

Arrhythmogenic Mechanisms in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia

Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor

Performance of a Protein Language Model for Variant Annotation in Cardiac Disease

Controversies in Brugada syndrome

Transcriptomic Coupling of PKP2 With Inflammatory and Immune Pathways Endogenous to Adult Cardiac Myocytes

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

Risk indicators in long QT syndrome: Does location matter?

Up-regulation of the inward rectifier K+ current (IK1) in the mouse heart accelerates and stabilizes rotors

Blockade of the Adenosine 2A Receptor Mitigates the Cardiomyopathy Induced by Loss of Plakophilin-2 Expression

Management of Congenital Long-QT Syndrome: Commentary From the Experts

Arrhythmogenic cardiomyopathy and Brugada syndrome: Diseases of the connexome

The Genetics of Brugada Syndrome

Discerning From the Good, the Bad, and the Ugly

ICD shocks and complications in patients with inherited arrhythmia syndromes

Sudden Cardiac Arrest in a Patient With Mitral Valve Prolapse and LMNA and SCN5A Mutations

Suchergebnisse filtern