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...

Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry

Circulation. Heart failure, 2024-03, Vol.17 (3), p.e010970

2024

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)

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)

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)

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)

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)

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)

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)

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)

Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variants

Heart rhythm, 2020-08, Vol.17 (8), p.1304-1311

2020

Volltextzugriff (PDF)

Low Incidence of Sudden Cardiac Death in a Swedish Y111C Type 1 Long-QT syndrome Population

Circulation. Cardiovascular genetics, 2009-12, Vol.2 (6), p.558-564

2009

Volltextzugriff (PDF)

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome

Cardiology in the young, 2013-06, Vol.23 (3), p.325-334

2013

Volltextzugriff (PDF)

Dynamic composite hydrogels of gelatin methacryloyl (GelMA) with supramolecular fibers for tissue engineering applications

Biomaterials advances, 2024-10, Vol.163, p.213957, Article 213957

2024

Volltextzugriff (PDF)

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Circulation (New York, N.Y.), 2020-07, Vol.142, p.324-338

2020

Volltextzugriff (PDF)

NICE, a new cause of death classification for stillbirths and neonatal deaths

International journal of epidemiology, 1998-06, Vol.27 (3), p.499-504

1998

Volltextzugriff (PDF)

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

BMC cardiovascular disorders, 2012-10, Vol.12 (1), p.95-95, Article 95

2012

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)

Assessment and Support? AI,R – A Pilot Project on Support Systems for Innovation in Automation Industry

Procedia, social and behavioral sciences, 2015-07, Vol.195, p.103-112

2015

Volltextzugriff (PDF)

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

Genetics in medicine, 2020-09

2020

Volltextzugriff (PDF)

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene

Journal of applied physiology (1985), 2013-11, Vol.115 (10), p.1423-1432

2013

Volltextzugriff (PDF)

Maternal risk factors for cause-specific stillbirth and neonatal death

Acta obstetricia et gynecologica Scandinavica, 2001-03, Vol.80 (3), p.235-244

2001

Volltextzugriff (PDF)

26 – 50 von 74

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(69)

Publikationsform

Sprache

Englisch
(73)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry

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

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

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

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

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

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

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

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

Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variants

Low Incidence of Sudden Cardiac Death in a Swedish Y111C Type 1 Long-QT syndrome Population

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome

Dynamic composite hydrogels of gelatin methacryloyl (GelMA) with supramolecular fibers for tissue engineering applications

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

NICE, a new cause of death classification for stillbirths and neonatal deaths

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

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

Assessment and Support? AI,R – A Pilot Project on Support Systems for Innovation in Automation Industry

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

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene

Maternal risk factors for cause-specific stillbirth and neonatal death

Suchergebnisse filtern