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...

Extensive Diversity of Molecular Mechanisms Underlying the Congenital Long QT Syndrome Type 1

Canadian journal of cardiology, 2018-09, Vol.34 (9), p.1108-1109

Horie, Minoru

2018

Volltextzugriff (PDF)

Genetic and Clinical Advances in Congenital Long QT Syndrome

Circulation Journal, 2014/11/25, Vol.78(12), pp.2827-2833

2014

Volltextzugriff (PDF)

Phenotypic Manifestations of Mutations in Genes Encoding Subunits of Cardiac Potassium Channels

Circulation research, 2011-06, Vol.109 (1), p.97-109

2011

Volltextzugriff (PDF)

Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

PloS one, 2021-02, Vol.16 (2), p.e0243476-e0243476

2021

Volltextzugriff (PDF)

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score

Circulation Journal, 2018/08/24, Vol.82(9), pp.2269-2276

2018

Volltextzugriff (PDF)

Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

PloS one, 2015-06, Vol.10 (6), p.e0131517-e0131517

2015

Volltextzugriff (PDF)

An NGS-based genotyping in LQTS; minor genes are no longer minor

Journal of human genetics, 2020-12, Vol.65 (12), p.1083-1091

2020

Volltextzugriff (PDF)

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

Europace (London, England), 2017-04, Vol.19 (4), p.665-694

2017

Volltextzugriff (PDF)

The genetics underlying acquired long QT syndrome: impact for genetic screening

European heart journal, 2016-05, Vol.37 (18), p.1456-1464

2016

Volltextzugriff (PDF)

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

Heart rhythm, 2016-10, Vol.13 (10), p.e295-e324

2016

Volltextzugriff (PDF)

Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation

Circulation Journal, 2020/01/24, Vol.84(2), pp.226-234

2020

Volltextzugriff (PDF)

Molecular pathogenesis of long QT syndrome type 1

Journal of arrhythmia, 2016-10, Vol.32 (5), p.381-388

2016

Volltextzugriff (PDF)

Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations

Internal Medicine, 2018/07/01, Vol.57(13), pp.1813-1817

2018

Volltextzugriff (PDF)

Genetics of Brugada syndrome

Journal of arrhythmia, 2016-10, Vol.32 (5), p.418-425

2016

Volltextzugriff (PDF)

Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture

Circulation Journal, 2013, Vol.77(5), pp.1307-1314

2013

Volltextzugriff (PDF)

Molecular genetics have opened a new era for arrhythmia research, but also Pandora's box?

Journal of arrhythmia, 2016-10, Vol.32 (5), p.313-314

Horie, Minoru

2016

Volltextzugriff (PDF)

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Nature communications, 2016-04, Vol.7 (1), p.11067-11067, Article 11067

2016

Volltextzugriff (PDF)

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Circulation Journal, 2024/06/25, Vol.88(7), pp.1176-1184

2024

Volltextzugriff (PDF)

Cardiomyopathy with an LMNA Genetic Variant Affecting Three Consecutive Generations: A Case Series

Internal Medicine, 2024/09/15, Vol.63(18), pp.2533-2536

2024

Volltextzugriff (PDF)

Dynamic QT Changes in Long QT Syndrome Type 8

Circulation Journal, 2019/06/25, Vol.83(7), pp.1614

2019

Volltextzugriff (PDF)

Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population

Circulation Journal, 2020/08/25, Vol.84(9), pp.1575-1581

2020

Volltextzugriff (PDF)

Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2

The Journal of general physiology, 2022-09, Vol.154 (9), p.1

2022

Volltextzugriff (PDF)

1 – 25 von 1.151

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(941)
Mit Volltextzugriff
(1.045)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.021)
Japanisch
(146)
Deutsch
(1)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(587)
Life Sciences & Biomedicine
(555)
Humans
(480)
Cardiovascular System & Cardiology
(379)
Male
(374)
Cardiac & Cardiovascular Systems
(345)
Female
(324)
Middle Aged
(253)
Aged
(204)
Adult
(193)
Electrocardiography
(138)
Cardiovascular
(130)
Mutation
(121)
Biological And Medical Sciences
(115)
Animals
(114)
Medical Sciences
(102)
Long Qt Syndrome
(95)
Heart
(90)
Adolescent
(75)
Risk Factors
(73)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

Extensive Diversity of Molecular Mechanisms Underlying the Congenital Long QT Syndrome Type 1

Genetic and Clinical Advances in Congenital Long QT Syndrome

Phenotypic Manifestations of Mutations in Genes Encoding Subunits of Cardiac Potassium Channels

Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score

Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

An NGS-based genotyping in LQTS; minor genes are no longer minor

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

The genetics underlying acquired long QT syndrome: impact for genetic screening

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation

Molecular pathogenesis of long QT syndrome type 1

Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations

Genetics of Brugada syndrome

Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture

Molecular genetics have opened a new era for arrhythmia research, but also Pandora's box?

Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Cardiomyopathy with an LMNA Genetic Variant Affecting Three Consecutive Generations: A Case Series

Efficacy of Antiarrhythmic Drugs Short-Term Use After Catheter Ablation for Atrial Fibrillation (EAST-AF) trial

Dynamic QT Changes in Long QT Syndrome Type 8

Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population

Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2

Suchergebnisse filtern