Search Results - "Jensen, H.K."

Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy by Larsen, M.K, Nissen, P.H, Berge, K.E, Leren, T.P, Kristensen, I.B, Jensen, H.K, Banner, J

“…Abstract The aim of this investigation was to identify and characterise pathogenic mutations in a sudden cardiac death (SCD) cohort suspected of cardiomyopathy…”
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249 oral MV IMAGE-BASED DYNAMIC MLC TRACKING OF A NITI STENT IN PIG LUNGS ON A LINEAR ACCELERATOR by Poulsen, P.R, Carl, J, Nielsen, J, Nielsen, M.S, Thomsen, J.B, Jensen, H.K, Kjærgaard, B, Zepernick, P.R, Worm, E, Fledelius, W, Cho, B, Sawanr, A, Ruan, D, Keall, P

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T-wave morphology reveals greater effect of d , l -sotalol than QTc by Graff, C, Andersen, M.P, Xue, J.Q, Hardahl, T.B, Kanters, J.K, Toft, E, Christiansen, M, Jensen, H.K, Struijk, J.J

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7103 Baseline and on-treatment expression of HIF-1a, HIF-2a and CAIX in patients with metastatic renal cell carcinoma by Jensen, H.K, Nordsmark, M, Donskov, F, Marcussen, N, Turley, H, Gatter, K, Harris, A, von der Maase, H

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P6091Transcatheter left atrial appendage occlusion using aspirin monotherapy for post-implant antithrombotic therapy by Korsholm, K., Nielsen, K.M., Jensen, J.M., Jensen, H.K., Andersen, G., Nielsen-Kudsk, J.E.

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Severity of congenital Long QT Syndrome disease onset and risk of depression, anxiety, and mortality: a nationwide study by Kroell, J, Jensen, H.K, Jespersen, C, Kanters, J.K, Hansen, M.S, Christiansen, M, Westergaard, L.M, Fosboel, E.L, Roerth, R, Torp-Pedersen, C, Koeber, L, Bundgaard, H, Tfelt-Hansen, J, Weeke, P.E

“…Abstract Introduction The congenital Long QT Syndrome (cLQTS) is associated with an increased risk of sudden cardiac death (SCD). Thus, cLQTS patients are…”
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First-in-world assessment of outcomes of catheter ablation for atrial arrhythmias in arrhythmogenic right ventricular cardiomyopathy by Gasperetti, A, James, C.A, Chen, L, Compagnucci, P, Casella, M, Dello Russo, A, Tondo, C, Platonov, P, Jensen, H.K, Schenker, N, Shibu, M, Kany, S, Calkins, H, Duru, F, Saguner, A.M

“…Abstract Introduction Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically inherited disease characterized by fibro-fatty infiltrations…”
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Genome-wide association study of patients with atrioventricular nodal reentry tachycardia by Andreasen, L, Ahlberg, G, Hartmann, J, Paludan-Mueller, C, Jensen, H.K, Riahi, S, Hansen, J, Sandgaard, N, Haunsoe, S, Kanters, J.K, Ellervik, C, Bundgaard, H, Svendsen, J.H, Olesen, M.S

“…Abstract Background Supraventricular tachycardias (SVTs) originate from the atria or the area close to the AV node. AV nodal reentry tachycardia (AVNRT) is one…”
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Phenotypic Variation in Patients Heterozygous for Familial Defective Apolipoprotein B (FDB) in Three European Countries by Hansen, P.S, Defesche, J.C, Kastelein, J.J.P, Gerdes, L.U, Fraza, L, Gerdes, C, Tato, F, Jensen, H.K, Jensen, L.G, Klausen, I.C, Faergeman, O, Schuster, H

“…A glutamine-for-arginine substitution at amino acid position 3500 of apolipoprotein B (apo B) causes synthesis of LDL with reduced binding affinity to the LDL…”
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MicroCT Imaging of Heart Valve Tissue in Fluid by Stephens, S.E., Bean, M., Surber, H., Ingels, N.B., Jensen, H.K., Liachenko, S., Wenk, J.F., Jensen, M.O.

“…Background Heart valve computational models require high quality geometric input data, commonly obtained using micro-computed tomography. Whether in the open…”
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Hospitalized acute patients with fever and severe infection have lower mortality than patients with hypo- or normothermia: a follow-up study by Henriksen, D P, Havshøj, U, Pedersen, P B, Laursen, C B, Jensen, H K, Brabrand, M, Lassen, A T

“…Severe infection is a frequent cause of admission to an acute medical unit (AMU). However, not all infected patients present with fever. The aim was to assess…”
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A sequence variation: 713-8delC in the transforming growth factor-beta 1 gene has higher prevalence in osteoporotic women than in normal women and is associated with very low bone mass in osteoporotic women and increased bone turnover in both osteoporotic and normal women by Langdahl, B.L., Knudsen, J.Y., Jensen, H.K., Gregersen, N., Eriksen, E.F.

“…Bone mass is partly genetically determined. The genes involved are, however, still largely unknown. Transforming growth factor-beta 1 (TGF-β1) is considered a…”
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28 Biventricular pacing versus DDD(R) pacing in patients with high-grade AV-block. A randomized comparison by Albertsen, A.E., Nielsen, J.C., Poulsen, S.H., Egeblad, H., Pedersen, A.K., Hansen, P.S., Jensen, H.K., Mortensen, P.T.

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783 Radiofrequency ablation of atrial fibrillation: Efficacy and safety in 102 consecutive patients by Pontoppidan, J., Nielsen, J.C., Poulsen, S.H., Jensen, H.K., Mortensen, P.T., Pedersen, A.K., Hansen, P.S.

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Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia by Jensen, H.K, Jensen, L.G, Meinertz, H, Hansen, P.S, Gregersen, N, Færgeman, O

“…Heterozygous familial hypercholesterolemia (FH) is one of the most common potentially fatal single-gene diseases leading to premature coronary artery disease,…”
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The importance of the left ventricular pacing site on the effect of biventricular pacing for heart failure in ischemic and non-ischemic dilated cardiomyopathy by Mortensen, P.T., S/ogàrd, P., Kim, Young, Jensen, H.K., Hansen, P.S., Pedersen, A.K.

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Same extent of coronary calcification in heterozygous familial hypercholesterolemia caused by a receptor defective and a receptor negative mutation in Danish patients by Brorholt-Petersen, J.U., Christiansen, T., Jensen, H.K., Jensen, J.M., Raungaard, B., Gregersen, N., Faergeman, O.

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Low density lipoprotein ligand function in patients with mutant apolipoprotein B-100 assessed by two-color fluorescence flow cytometry by Raungaard, B., Heath, F., Brorholt-Petersen, J.U., Jensen, H.K., Faergeman, O.

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Prediction of ischemic heart disease by coronary calcium in patients with familial hypercholesterolemia by Jensen, J.M., Gerdes, L.U., Christiansen, T.M., Brorholt-Petersen, J.U., Jensen, H.K., Faergeman, O.

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The Trp 23-Stop and Trp 66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark by Jensen, H.K., Jensen, L.G., Hansen, P.S., Færgeman, O., Gregersen, N.

“…Mutations in the gene for the low density lipoprotein (LDL) receptor cause the autosomal dominant disease familial hypercholesterolemia (FH), the prevalence of…”
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