about
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillationManagement of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countriesMutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study.Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutationsCardiovascular risk factor control is insufficient in young patients with coronary artery disease.A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease.Coronary artery disease-associated genetic variants and biomarkers of inflammationNo 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.Coronary Plaque Burden and Adverse Plaque Characteristics Are Increased in Healthy Relatives of Patients With Early Onset Coronary Artery Disease.A 45-SNP genetic risk score is increased in early-onset coronary artery disease but independent of familial disease clustering.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.The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population.A genetic risk score predicts cardiovascular events in patients with stable coronary artery disease.Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.Transcatheter left atrial appendage occlusion in patients with atrial fibrillation and a high bleeding risk using aspirin alone for post-implant antithrombotic therapy.Superior transseptal approach to mitral valve is associated with a higher need for pacemaker implantation than the left atrial approach.The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria.Left ventricular lead performance in cardiac resynchronization therapy: impact of lead localization and complications.The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity.The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death CasesPhenotypic characterization of late onset cardiac amyloidosis caused by the transthyretin mutation TTRA45S, p.(Ala65Ser)QTc Interval and Risk of Cardiac Events in Adults With Anorexia Nervosa: A Long-Term Follow-Up Study
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Q21261490-21C0A44E-BCE5-43FD-97C9-AD988AEC82D6Q26782057-B155F9B9-3FF5-4396-A89F-802C93E195EFQ31153701-8B958BB8-4CA1-4A82-A553-E19E6C13B48FQ33160907-7745BD38-B4CA-48D1-82E6-9E84EA607009Q33163183-F728090B-505A-4057-8FDE-138050777A01Q34920627-92D8C0D6-704B-44DC-8A9E-01B13EBD35F9Q36956002-E54ACB69-F5C8-437A-8324-9FCF7FFE21E5Q37385366-4BD42207-704E-4B65-8B69-077FD7171E73Q40960080-7C125B90-30E7-41D1-A4FB-B8AE3F9CEC3EQ45142380-DC0910D1-DE45-4330-A4C3-D2196093FB04Q46000375-9CB10FFA-CFE0-4C25-973E-6935966DB71DQ47874849-FD3B310A-7228-43EF-BEDC-5DCCBED6B547Q47914586-A94C6AD5-4852-4893-8585-909BCB0E01B2Q50579803-90706F61-BE33-440C-919B-28042316A8DAQ50701682-D00306D4-ACBB-4462-AEE9-1D802A33CBBBQ50971591-FEA69F6F-40B2-4A78-863B-DF23AF6C9F92Q51079772-A2D0EC8C-32A9-4A73-BB4D-C36989B751A5Q51092109-BBFDD039-1918-4A02-8C2B-C3D632374FEAQ51133570-9AC8C4F6-A6E8-4B3B-8CCF-DA8D2C859518Q51434995-8D0C131F-3C57-453D-96DE-F9943AA26C10Q53087375-495B5D2D-4670-49C2-944C-D4212261F024Q57682751-FCE86D00-2673-4D49-8203-19A18C6753C8Q58290327-31504F60-F134-4D5D-A418-9A7253F7CCBBQ90374327-51983326-92B2-4DAF-892E-FC69541B8F5A
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description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Henrik K Jensen
@ast
Henrik K Jensen
@en
Henrik K Jensen
@es
Henrik K Jensen
@nl
Henrik K Jensen
@sl
type
label
Henrik K Jensen
@ast
Henrik K Jensen
@en
Henrik K Jensen
@es
Henrik K Jensen
@nl
Henrik K Jensen
@sl
prefLabel
Henrik K Jensen
@ast
Henrik K Jensen
@en
Henrik K Jensen
@es
Henrik K Jensen
@nl
Henrik K Jensen
@sl
P214
P106
P21
P214
P31
P496
0000-0003-1802-4302
P569
2000-01-01T00:00:00Z
P734
P735
P7859
viaf-307249305