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 modulation of atrial fibrillation risk in a Hispanic/Latino cohort

PloS one, 2018-04, Vol.13 (4), p.e0194480-e0194480

2018

Volltextzugriff (PDF)

A new paradigm for predicting risk of Torsades de Pointes during drug development: Commentary on: "Improved prediction of drug-induced Torsades de Pointes through simulations of dynamics and machine learning algorithms"

Clinical pharmacology and therapeutics, 2016-10, Vol.100 (4), p.324-326

2016

Volltextzugriff (PDF)

Association Between Family History and Early-Onset Atrial Fibrillation Across Racial and Ethnic Groups

JAMA network open, 2018-09, Vol.1 (5), p.e182497

2018

Volltextzugriff (PDF)

12 Validation of a Clinical Decision Aid for 30-Day Adverse Events in Emergency Department Patients With Atrial Fibrillation

Annals of emergency medicine, 2014-10, Vol.64 (4), p.S5-S6

2014

Volltextzugriff (PDF)

Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation

Europace (London, England), 2014-04, Vol.16 (4), p.485-490

2014

Volltextzugriff (PDF)

ST ELEVATION AS AN ECG ENDOPHENOTYPE FOR ATRIAL FIBRILLATION PATIENTS HARBORING RARE SODIUM CHANNEL SUBUNIT GENE VARIANTS

Heart rhythm, 2014-11, Vol.11 (11), p.2140-2140

2014

Volltextzugriff (PDF)

MICE THAT OVEREXPRESS A FRAMESHIFT MUTATION IN HUMAN NATRIURETIC PEPTIDE PRECURSOR A GENE EXHIBIT INCREASED ATRIAL FIBRILLATION BURDEN BUT NO ATRIAL STRUCTURAL REMODELING

Heart rhythm, 2014-11, Vol.11 (11), p.2132-2132

2014

Volltextzugriff (PDF)

SCN10A Rare Variants Associated with Atrial Fibrillation and Slow Ventricular Rates Reveal Increased Late Sodium Current

Heart rhythm, 2012-11, Vol.9 (11), p.1911-1911

2012

Volltextzugriff (PDF)

On the relationship among QT interval, atrial fibrillation, and torsade de pointes

Europace (London, England), 2007-09, Vol.9 Suppl 4 (Supplement 4), p.iv1-iv3

2007

Volltextzugriff (PDF)

A Common β-Adrenergic Receptor Polymorphism Modulates Response to Rate Control in Atrial Fibrillation

Heart rhythm, 2011, Vol.8 (11), p.1825-1825

2011

Volltextzugriff (PDF)

Sequencing candidate genes in African American and Hispanic/ Latino probands with early-onset Atrial Fibrillation

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

Volltextzugriff (PDF)

P4622Comorbid malignancy as an independent predictor of in-hospital mortality in patients with atrial fibrillation

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

Volltextzugriff (PDF)

Myosin light chain dephosphorylation by ppp1r12c promotes atrial hypocontractility in atrial fibrillation

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Volltextzugriff (PDF)

1: A Clinical Prediction Model to Estimate Risk for 30-Day Adverse Events in Emergency Department Patients With Symptomatic Atrial Fibrillation

Annals of emergency medicine, 2009, Vol.54 (3), p.S1-S2

2009

Volltextzugriff (PDF)

Electrophysiologic Characterization of Calcium Handling in Human Induced Pluripotent Stem Cell-Derived Atrial Cardiomyocytes

Stem cell reports, 2018-06, Vol.10 (6), p.1867-1878

2018

Volltextzugriff (PDF)

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

Europace (London, England), 2012-10, Vol.14 (10), p.1428-1432

2012

Volltextzugriff (PDF)

Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies

Frontiers in pharmacology, 2012-01, Vol.3, p.124-124

2012

Volltextzugriff (PDF)

Detection of left ventricular dysfunction after acute myocardial infarction: comparison of clinical, echocardiographic, and neurohormonal methods

British Heart Journal, 1994-07, Vol.72 (1), p.16-22

1994

Volltextzugriff (PDF)

Familial atrial fibrillation is a genetically heterogeneous disorder

Journal of the American College of Cardiology, 2003-06, Vol.41 (12), p.2185-2192

2003

Volltextzugriff (PDF)

5073Elucidating the underlying mechanisms for the differential response to sodium channel blocker antiarrhythmic drugs in obese patients with atrial fibrillation

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

Volltextzugriff (PDF)

Sensitivity and specificity of QTc dispersion for identification of risk of cardiac death in patients with peripheral vascular disease

BMJ, 1996-04, Vol.312 (7035), p.874-878

International edition, 1996

Volltextzugriff (PDF)

Unmasking of brugada syndrome by lithium

Circulation (New York, N.Y.), 2005-09, Vol.112 (11), p.1527-1531

2005

Volltextzugriff (PDF)

Pharmacogenomics of atrial fibrillation

Clinical pharmacology and therapeutics, 2005-02, Vol.77 (2), p.P7-P7

2005

Volltextzugriff (PDF)

Screening for genomic alterations in congenital long QT syndrome

Heart rhythm, 2006, Vol.3 (1), p.56-57

Darbar, Dawood

2006

Volltextzugriff (PDF)

1 – 25 von 244

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(231)
Mit Volltextzugriff
(186)

Publikationsform

Sprache

Englisch
(244)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort

A new paradigm for predicting risk of Torsades de Pointes during drug development: Commentary on: "Improved prediction of drug-induced Torsades de Pointes through simulations of dynamics and machine learning algorithms"

Association Between Family History and Early-Onset Atrial Fibrillation Across Racial and Ethnic Groups

12 Validation of a Clinical Decision Aid for 30-Day Adverse Events in Emergency Department Patients With Atrial Fibrillation

Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation

ST ELEVATION AS AN ECG ENDOPHENOTYPE FOR ATRIAL FIBRILLATION PATIENTS HARBORING RARE SODIUM CHANNEL SUBUNIT GENE VARIANTS

MICE THAT OVEREXPRESS A FRAMESHIFT MUTATION IN HUMAN NATRIURETIC PEPTIDE PRECURSOR A GENE EXHIBIT INCREASED ATRIAL FIBRILLATION BURDEN BUT NO ATRIAL STRUCTURAL REMODELING

SCN10A Rare Variants Associated with Atrial Fibrillation and Slow Ventricular Rates Reveal Increased Late Sodium Current

On the relationship among QT interval, atrial fibrillation, and torsade de pointes

A Common β-Adrenergic Receptor Polymorphism Modulates Response to Rate Control in Atrial Fibrillation

Sequencing candidate genes in African American and Hispanic/ Latino probands with early-onset Atrial Fibrillation

P4622Comorbid malignancy as an independent predictor of in-hospital mortality in patients with atrial fibrillation

Myosin light chain dephosphorylation by ppp1r12c promotes atrial hypocontractility in atrial fibrillation

1: A Clinical Prediction Model to Estimate Risk for 30-Day Adverse Events in Emergency Department Patients With Symptomatic Atrial Fibrillation

Electrophysiologic Characterization of Calcium Handling in Human Induced Pluripotent Stem Cell-Derived Atrial Cardiomyocytes

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies

Detection of left ventricular dysfunction after acute myocardial infarction: comparison of clinical, echocardiographic, and neurohormonal methods

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

Familial atrial fibrillation is a genetically heterogeneous disorder

5073Elucidating the underlying mechanisms for the differential response to sodium channel blocker antiarrhythmic drugs in obese patients with atrial fibrillation

Sensitivity and specificity of QTc dispersion for identification of risk of cardiac death in patients with peripheral vascular disease

Unmasking of brugada syndrome by lithium

Pharmacogenomics of atrial fibrillation

Screening for genomic alterations in congenital long QT syndrome

Suchergebnisse filtern