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)

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)

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)

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)

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)

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)

Genetics of Brugada syndrome

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

2016

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)

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)

Dynamic QT Changes in Long QT Syndrome Type 8

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

2019

Volltextzugriff (PDF)

A de novo gain-of-function KCND3 mutation in early repolarization syndrome

Heart rhythm, 2019-11, Vol.16 (11), p.1698-1706

2019

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)

Incidence and Prognostic Impact of Heart Failure Hospitalization During Follow Up After Primary Percutaneous Coronary Intervention in ST-Segment Elevation Myocardial Infarction

The American journal of cardiology, 2017-06, Vol.119 (11), p.1729-1739

2017

Volltextzugriff (PDF)

Response to Letter to the Editor: "How to Screen and Manage Suspected Laminopathy"

Internal Medicine, 2024, pp.3959-24

2024

Volltextzugriff (PDF)

Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome

PloS one, 2022-07, Vol.17 (7), p.e0271796-e0271796

2022

Volltextzugriff (PDF)

A tryptophan residue in the caffeine-binding site of the ryanodine receptor regulates Ca2+ sensitivity

Communications biology, 2018-07, Vol.1 (1), p.98-98, Article 98

2018

Volltextzugriff (PDF)

1 – 25 von 899

Suche als RSS-Feed

Aktive Filter

ThemaMiddle Aged

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(707)
Mit Volltextzugriff
(809)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(775)
Japanisch
(138)
Deutsch
(1)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(360)
Life Sciences & Biomedicine
(332)
Humans
(231)
Cardiovascular System & Cardiology
(216)
Cardiac & Cardiovascular Systems
(207)
Male
(142)
Female
(117)
Animals
(103)
Cardiovascular
(99)
Mutation
(88)
Electrocardiography
(86)
Long Qt Syndrome
(80)
Biological And Medical Sciences
(72)
Heart
(59)
Medical Sciences
(59)
Adult
(57)
Aged
(44)
Long Qt Syndrome - Genetics
(44)
Cardiac Arrhythmia
(43)
Patch-Clamp Techniques
(41)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... 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

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

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

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

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

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

Genetics of Brugada syndrome

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

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

Dynamic QT Changes in Long QT Syndrome Type 8

A de novo gain-of-function KCND3 mutation in early repolarization syndrome

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

Incidence and Prognostic Impact of Heart Failure Hospitalization During Follow Up After Primary Percutaneous Coronary Intervention in ST-Segment Elevation Myocardial Infarction

Response to Letter to the Editor: "How to Screen and Manage Suspected Laminopathy"

Novel CACNA1C R511Q mutation, located in domain Ⅰ-Ⅱ linker, causes non-syndromic type-8 long QT syndrome

A tryptophan residue in the caffeine-binding site of the ryanodine receptor regulates Ca2+ sensitivity

Aktive Filter

Suchergebnisse filtern