Lista de obras - Henrik K Jensen - Dominio Público Uruguay

A 45-SNP genetic risk score is increased in early-onset coronary artery disease but independent of familial disease clustering

artículo científico publicado en 2017

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

artículo científico publicado en 2009

A genetic risk score predicts cardiovascular events in patients with stable coronary artery disease

artículo científico publicado en 2017

Ablation for idiopathic ventricular arrhythmia - with and without arrhythmia-induced cardiomyopathy

artículo científico publicado en 2014

Biventricular pacing preserves left ventricular performance in patients with high-grade atrio-ventricular block: a randomized comparison with DDD(R) pacing in 50 consecutive patients

artículo científico publicado en 2008

Cardiovascular risk factor control is insufficient in young patients with coronary artery disease

artículo científico publicado en 2016

Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome

artículo científico publicado en 2013

Catheter ablation for ventricular tachycardia in ischaemic heart disease; acute success and long-term outcome.

artículo científico publicado en 2014

Coronary Plaque Burden and Adverse Plaque Characteristics Are Increased in Healthy Relatives of Patients With Early Onset Coronary Artery Disease.

artículo científico publicado en 2017

Coronary artery disease-associated genetic variants and biomarkers of inflammation ⬇️

artículo científico publicado en 2017

Flow cytometric assessment of effects of fluvastatin on low-density lipoprotein receptor activity in stimulated T-lymphocytes from patients with heterozygous familial hypercholesterolemia

artículo científico publicado en 2000

Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families

artículo científico publicado en 1996

Identifying drug-induced repolarization abnormalities from distinct ECG patterns in congenital long QT syndrome: a study of sotalol effects on T-wave morphology.

artículo científico publicado en 2009

Impact of Acute Biventricular Pacing on Left Ventricular Performance and Volumes in Patients with Severe Heart Failure

artículo científico publicado en 2001

Incidence of the apolipoprotein B-3500 mutation in Denmark

artículo científico publicado en 1994

Is the knowledge of contact force beneficial in pulmonary vein antrum isolation?

artículo científico publicado en 2017

Left ventricular lead performance in cardiac resynchronization therapy: impact of lead localization and complications

artículo científico publicado en 2005

Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations

artículo científico publicado en 2013

Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study

artículo científico publicado en 2012

Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries

artículo científico publicado en 2015

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.

artículo científico publicado en 2014

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

artículo científico publicado en 2012

No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes

artículo científico publicado en 2004

Outcome after catheter ablation for left atrial flutter

scientific article published on 12 May 2019

Phenotypic characterization of late onset cardiac amyloidosis caused by the transthyretin mutation TTRA45S, p.(Ala65Ser)

Proteolysis of arterial basement membrane containing different amounts of carbohydrates

artículo científico publicado en 1986

QT interval corrected for heart rate is not associated with mortality in patients with cirrhosis and ascites

artículo científico publicado en 2019

QTc Interval and Risk of Cardiac Events in Adults With Anorexia Nervosa: A Long-Term Follow-Up Study

scientific article published on 01 August 2018

Rapid Exclusion of COVID Infection With the Artificial Intelligence Electrocardiogram

artículo científico publicado en 2021

Recurrence after pulmonary vein isolation is associated with low contact force

artículo científico publicado en 2017

Repeat pulmonary vein isolation in patients with atrial fibrillation: low ablation index is associated with increased risk of recurrent arrhythmia

artículo científico publicado en 2020

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics

artículo científico publicado en 2012

Superior transseptal approach to mitral valve is associated with a higher need for pacemaker implantation than the left atrial approach

artículo científico publicado en 2007

The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes

artículo científico publicado en 2022

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

article by BO GREGERS WINKEL et al published 6 August 2012 in Journal of Cardiovascular Electrophysiology

The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity

artículo científico publicado en 2017

The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark

artículo científico publicado en 1996

The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria

artículo científico publicado en 2014

The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population

artículo científico publicado en 2005

Transcatheter left atrial appendage occlusion in patients with atrial fibrillation and a high bleeding risk using aspirin alone for post-implant antithrombotic therapy

artículo científico publicado en 2016

Lista de obras de Henrik K Jensen

A 45-SNP genetic risk score is increased in early-onset coronary artery disease but independent of familial disease clustering

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

A genetic risk score predicts cardiovascular events in patients with stable coronary artery disease

Ablation for idiopathic ventricular arrhythmia - with and without arrhythmia-induced cardiomyopathy

Biventricular pacing preserves left ventricular performance in patients with high-grade atrio-ventricular block: a randomized comparison with DDD(R) pacing in 50 consecutive patients

Cardiovascular risk factor control is insufficient in young patients with coronary artery disease

Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome

Catheter ablation for ventricular tachycardia in ischaemic heart disease; acute success and long-term outcome.

Coronary Plaque Burden and Adverse Plaque Characteristics Are Increased in Healthy Relatives of Patients With Early Onset Coronary Artery Disease.

Coronary artery disease-associated genetic variants and biomarkers of inflammation ⬇️

Flow cytometric assessment of effects of fluvastatin on low-density lipoprotein receptor activity in stimulated T-lymphocytes from patients with heterozygous familial hypercholesterolemia

Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families

Identifying drug-induced repolarization abnormalities from distinct ECG patterns in congenital long QT syndrome: a study of sotalol effects on T-wave morphology.

Impact of Acute Biventricular Pacing on Left Ventricular Performance and Volumes in Patients with Severe Heart Failure

Incidence of the apolipoprotein B-3500 mutation in Denmark

Is the knowledge of contact force beneficial in pulmonary vein antrum isolation?

Left ventricular lead performance in cardiac resynchronization therapy: impact of lead localization and complications

Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations

Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study

Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes

Outcome after catheter ablation for left atrial flutter

Phenotypic characterization of late onset cardiac amyloidosis caused by the transthyretin mutation TTRA45S, p.(Ala65Ser)

Proteolysis of arterial basement membrane containing different amounts of carbohydrates

QT interval corrected for heart rate is not associated with mortality in patients with cirrhosis and ascites

QTc Interval and Risk of Cardiac Events in Adults With Anorexia Nervosa: A Long-Term Follow-Up Study

Rapid Exclusion of COVID Infection With the Artificial Intelligence Electrocardiogram

Recurrence after pulmonary vein isolation is associated with low contact force

Repeat pulmonary vein isolation in patients with atrial fibrillation: low ablation index is associated with increased risk of recurrent arrhythmia

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics

Superior transseptal approach to mitral valve is associated with a higher need for pacemaker implantation than the left atrial approach

The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity

The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark

The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria

The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population

Transcatheter left atrial appendage occlusion in patients with atrial fibrillation and a high bleeding risk using aspirin alone for post-implant antithrombotic therapy