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Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy

Forensic science international, 2012-06, Vol.219 (1), p.33-38

2012

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249 oral MV IMAGE-BASED DYNAMIC MLC TRACKING OF A NITI STENT IN PIG LUNGS ON A LINEAR ACCELERATOR

Radiotherapy and oncology, 2011, Vol.99, p.S97-S98

2011

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P6091Transcatheter left atrial appendage occlusion using aspirin monotherapy for post-implant antithrombotic therapy

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

2017

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MicroCT Imaging of Heart Valve Tissue in Fluid

Experimental mechanics, 2021-01, Vol.61 (1), p.253-261

2021

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Severity of congenital Long QT Syndrome disease onset and risk of depression, anxiety, and mortality: a nationwide study

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

2020

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First-in-world assessment of outcomes of catheter ablation for atrial arrhythmias in arrhythmogenic right ventricular cardiomyopathy

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

2020

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Genome-wide association study of patients with atrioventricular nodal reentry tachycardia

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

2020

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T-wave morphology reveals greater effect of d , l -sotalol than QTc

Journal of electrocardiology, 2008, Vol.41 (6), p.644-644

2008

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7103 Baseline and on-treatment expression of HIF-1a, HIF-2a and CAIX in patients with metastatic renal cell carcinoma

European journal of cancer supplements, 2009, Vol.7 (2), p.423-423

2009

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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

QJM : An International Journal of Medicine, 2016-07, Vol.109 (7), p.473-479

2016

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Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries

Arteriosclerosis, thrombosis, and vascular biology, 1997-04, Vol.17 (4), p.741

1997

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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

Bone (New York, N.Y.), 1997-03, Vol.20 (3), p.289-294

1997

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Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia

Atherosclerosis, 1999-10, Vol.146 (2), p.337-344

1999

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783 Radiofrequency ablation of atrial fibrillation: Efficacy and safety in 102 consecutive patients

Europace (London, England), 2005-06, Vol.7 (Supplement_1), p.178-178

2005

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28 Biventricular pacing versus DDD(R) pacing in patients with high-grade AV-block. A randomized comparison

Europace (London, England), 2005-06, Vol.7 (Supplement_1), p.6-6

2005

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A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein

Atherosclerosis, 1997-05, Vol.131 (1), p.67-72

1997

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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

Atherosclerosis, 1999-05, Vol.144, p.186-187

1999

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Prediction of ischemic heart disease by coronary calcium in patients with familial hypercholesterolemia

Atherosclerosis, 1999-05, Vol.144, p.69-70

1999

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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

Europace (London, England), 2001-01, Vol.2 (Supplement_1), p.A32-A32

2001

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Low density lipoprotein ligand function in patients with mutant apolipoprotein B-100 assessed by two-color fluorescence flow cytometry

Atherosclerosis, 1999-05, Vol.144, p.80-80

1999

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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

Atherosclerosis, 1996, Vol.120 (1), p.57-65

1996

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4.P.309 Functional characterization of low density lipoprotein receptor gene mutations in patients with familial hypercholesterolemia

Atherosclerosis, 1997-10, Vol.134 (1-2), p.361-361

1997

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Two point mutations (313 + 1G→A and 313 + 1G→T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia

Human mutation, 1996, Vol.7 (3), p.269-271

1996

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Attitudes towards screening in families affected with familial hypercholesterolemia

Atherosclerosis, 1995-06, Vol.115, p.S77-S77

1995

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A Time-Based Control Scheme for Power Factor Correction Boost Converter

2019 IEEE Nordic Circuits and Systems Conference (NORCAS): NORCHIP and International Symposium of System-on-Chip (SoC), 2019, p.1-6

2019

Volltextzugriff (PDF)

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Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy

249 oral MV IMAGE-BASED DYNAMIC MLC TRACKING OF A NITI STENT IN PIG LUNGS ON A LINEAR ACCELERATOR

P6091Transcatheter left atrial appendage occlusion using aspirin monotherapy for post-implant antithrombotic therapy

MicroCT Imaging of Heart Valve Tissue in Fluid

Severity of congenital Long QT Syndrome disease onset and risk of depression, anxiety, and mortality: a nationwide study

First-in-world assessment of outcomes of catheter ablation for atrial arrhythmias in arrhythmogenic right ventricular cardiomyopathy

Genome-wide association study of patients with atrioventricular nodal reentry tachycardia

T-wave morphology reveals greater effect of d , l -sotalol than QTc

7103 Baseline and on-treatment expression of HIF-1a, HIF-2a and CAIX in patients with metastatic renal cell carcinoma

Hospitalized acute patients with fever and severe infection have lower mortality than patients with hypo- or normothermia: a follow-up study

Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries

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

Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia

783 Radiofrequency ablation of atrial fibrillation: Efficacy and safety in 102 consecutive patients

28 Biventricular pacing versus DDD(R) pacing in patients with high-grade AV-block. A randomized comparison

A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein

Same extent of coronary calcification in heterozygous familial hypercholesterolemia caused by a receptor defective and a receptor negative mutation in Danish patients

Prediction of ischemic heart disease by coronary calcium in patients with familial hypercholesterolemia

The importance of the left ventricular pacing site on the effect of biventricular pacing for heart failure in ischemic and non-ischemic dilated cardiomyopathy

Low density lipoprotein ligand function in patients with mutant apolipoprotein B-100 assessed by two-color fluorescence flow cytometry

The Trp 23-Stop and Trp 66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark

4.P.309 Functional characterization of low density lipoprotein receptor gene mutations in patients with familial hypercholesterolemia

Two point mutations (313 + 1G→A and 313 + 1G→T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia

Attitudes towards screening in families affected with familial hypercholesterolemia

A Time-Based Control Scheme for Power Factor Correction Boost Converter

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