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...

Cardiac response to water activities in children with Long QT syndrome type 1

PloS one, 2023-12, Vol.18 (12), p.e0295431-e0295431

2023

Volltextzugriff (PDF)

LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder

Biodemography and social biology, 2020-10, Vol.66 (3-4), p.191-207

2020

Volltextzugriff (PDF)

To Modify or Not to Modify: Allele-Specific Effects of 3'UTR- KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation

Journal of the American Heart Association, 2022-09, Vol.11 (18), p.e025981-e025981

2022

Volltextzugriff (PDF)

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2015-08, Vol.8 (4), p.806-814

2015

Volltextzugriff (PDF)

Origin of the Swedish long QT syndrome Y111C/ KCNQ1 founder mutation

Heart rhythm, 2011-04, Vol.8 (4), p.541-547

2011

Volltextzugriff (PDF)

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

BMC medical genetics, 2017-07, Vol.18 (1), p.74-74, Article 74

2017

Volltextzugriff (PDF)

Combining tissue engineering and optical imaging approaches to explore interactions along the neuro-cardiac axis

Royal Society open science, 2020-06, Vol.7 (6), p.200265-200265

2020

Volltextzugriff (PDF)

Modelling neurocardiac physiology and diseases using human pluripotent stem cells: current progress and future prospects

The Journal of physiology, 2024-09

2024

Volltextzugriff (PDF)

Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

American journal of physiology. Heart and circulatory physiology, 2021-07, Vol.321 (1), p.H217

2021

Volltextzugriff (PDF)

Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

American journal of physiology. Heart and circulatory physiology, 2020-11, Vol.319 (5), p.H927-H937

2020

Volltextzugriff (PDF)

Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations

HeartRhythm case reports, 2018-06, Vol.4 (6), p.237-240

2018

Volltextzugriff (PDF)

The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes

Heart, lung & circulation, 2020-04, Vol.29 (4), p.529-537

2020

Volltextzugriff (PDF)

Neuroscience in the heart: Recent advances in neurocardiac communication and its role in cardiac arrhythmias

The international journal of biochemistry & cell biology, 2020-05, Vol.122, p.105737-105737, Article 105737

2020

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)

Functional hyperactivity in long QT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

American journal of physiology. Heart and circulatory physiology, 2021-07, Vol.321 (1), p.H217-H227

2021

Volltextzugriff (PDF)

Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

American journal of obstetrics and gynecology, 2020-03, Vol.222 (3), p.263.e1-263.e11

2020

Volltextzugriff (PDF)

Molecular and cellular neurocardiology in heart disease

The Journal of physiology, 2024-05

2024

Volltextzugriff (PDF)

Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes

Journal of molecular and cellular cardiology, 2016-11, Vol.100, p.25-34

2016

Volltextzugriff (PDF)

Cardiac response to water activities in children with Long QT syndrome type 1

PloS one, 2023-01, Vol.18 (12), p.e0295431

2023

Volltextzugriff (PDF)

Assays of Variant Effect and Automated Patch Clamping Improve KCNH2 -LQTS Variant Classification and Cardiac Event Risk Stratification

Circulation (New York, N.Y.), 2024-09

2024

Volltextzugriff (PDF)

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

Europace (London, England), 2023-11, Vol.25 (11)

2023

Volltextzugriff (PDF)

130: Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype. Results of an 8-center international study

American journal of obstetrics and gynecology, 2018-01, Vol.218 (1), p.S93-S93

2018

Volltextzugriff (PDF)

Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype: Results of an 8-center international study

American journal of obstetrics and gynecology, 2018, Vol.218 (1), p.S93

2018

Volltextzugriff (PDF)

Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects

Heart, lung & circulation, 2019-01, Vol.28 (1), p.22-30

2019

Volltextzugriff (PDF)

1 – 25 von 41

Suche als RSS-Feed

Aktive Filter

ThemaAged

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(40)
Berichte
(1)

Sprache

Englisch
(41)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Cardiac response to water activities in children with Long QT syndrome type 1

LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder

To Modify or Not to Modify: Allele-Specific Effects of 3'UTR- KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Origin of the Swedish long QT syndrome Y111C/ KCNQ1 founder mutation

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

Combining tissue engineering and optical imaging approaches to explore interactions along the neuro-cardiac axis

Modelling neurocardiac physiology and diseases using human pluripotent stem cells: current progress and future prospects

Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations

The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes

Neuroscience in the heart: Recent advances in neurocardiac communication and its role in cardiac arrhythmias

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

Functional hyperactivity in long QT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

Molecular and cellular neurocardiology in heart disease

Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes

Cardiac response to water activities in children with Long QT syndrome type 1

Assays of Variant Effect and Automated Patch Clamping Improve KCNH2 -LQTS Variant Classification and Cardiac Event Risk Stratification

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

130: Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype. Results of an 8-center international study

Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype: Results of an 8-center international study

BS-469619-003 GRANULAR VARIANT-SPECIFIC FEATURES IMPROVE KCNH2-LONG QT SYNDROME RISK STRATIFICATION

Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects

Aktive Filter

Suchergebnisse filtern