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Plasma levels of PCSK9 and phenotypic variability in familial hypercholesterolemia

Journal of lipid research, 2012-05, Vol.53 (5), p.979-983

2012

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Evaluation of cholesterol lowering treatment of patients with familial hypercholesterolemia: a large cross-sectional study in The Netherlands

Atherosclerosis, 2010-03, Vol.209 (1), p.189-194

2010

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Factor VIII deficiency does not protect against atherosclerosis

Journal of thrombosis and haemostasis, 2012-01, Vol.10 (1), p.30-37

2012

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Venous thrombosis is associated with hyperglycemia at diagnosis: a case–control study

Journal of thrombosis and haemostasis, 2009-06, Vol.7 (6), p.945-949

2009

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Real-time MSE measurements for current profile control on KSTAR

Review of scientific instruments, 2012-10, Vol.83 (10), p.10D524-10D524

2012

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Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis

Clinical genetics, 2012-01, Vol.81 (1), p.24-28

2012

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Familial hypercholesterolemia patients with unexplained low ldl-c: a role for angptl3?

Atherosclerosis, 2019-08, Vol.287, p.e41-e41

2019

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Statins Reduce Hepatic Angptl3 Expression And Secretion, Likely By Interfering With Lxr-Mediated Transcription

Atherosclerosis, 2019-08, Vol.287, p.e37-e37

2019

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Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes

Netherlands heart journal, 2011-04, Vol.19 (4), p.175-182

2011

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Hip surgery sequentially induces stress hyperglycaemia and activates coagulation

Netherlands journal of medicine, 2009-06, Vol.67 (6), p.226-229

2009

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Colesevelam added to combination therapy with a statin and ezetimibe in patients with familial hypercholesterolemia: A 12-week, multicenter, randomized, double-blind, controlled trial

Clinical therapeutics, 2010-04, Vol.32 (4), p.615-625

2010

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Real-time MSE measurements for current profile control on KSTARa

Review of scientific instruments, 2012-10, Vol.83 (10)

2012

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Abstract: P870 IDENTIFICATION OF APOB AND PCSK9 MUTATIONS CAUSING A NON-ADH PHENOTYPE IN MOLECULAR DIAGNOSED ADH PATIENTS

Atherosclerosis. Supplements, 2009-06, Vol.10 (2), p.e1015-e1015

2009

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P40 CAROTID ATHEROSCLEROSIS OF PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA NO LONGER DIFFERS FROM UNAFFECTED RELATIVES ALREADY WITHIN 18 MONTHS AFTER IDENTIFICATION

Atherosclerosis. Supplements, 2010-06, Vol.11 (2), p.25-25

2010

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L6 EFFICACY OF 15 YEARS OF GENETIC CASCADE SCREENING FOR FAMILIAL HYPERCHOLESTEROLEMIA IN THE NETHERLANDS IN PREVENTION OF CORONARY ARTERY DISEASE

Atherosclerosis. Supplements, 2010-06, Vol.11 (2), p.14-14

2010

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603 COMBINING EXOME SEQUENCING WITH EXCLUSION LINKAGE ANALYSIS AS A TOOL TO UNRAVEL THE MOLECULAR BASIS OF A COMMON GENETIC DISEASE

Atherosclerosis. Supplements, 2011-06, Vol.12 (1), p.127-127

2011

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Abstract: P841 NON-FUNCTIONALITY OF THREE LDL-R AND APOB GENE MUTATIONS THAT WERE ASSUMED TO CAUSE FAMILIAL HYPERCHOLESTEROLEMIA

Atherosclerosis. Supplements, 2009-06, Vol.10 (2), p.e1231-e1231

2009

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Abstract: 576 LIPID-LOWERING MEDICATION TWO YEARS AFTER MOLECULAR DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA

Atherosclerosis. Supplements, 2009-06, Vol.10 (2), p.e337-e337

2009

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MS351 FOLLOW-UP OF CHILDREN AFTER POSITIVE GENETIC TESTING IN THE DUTCH NATIONAL SCREENING PROGRAM FOR FAMILIAL HYPERCHOLESTEROLEMIA

Atherosclerosis. Supplements, 2010-06, Vol.11 (2), p.180-180

2010

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66 THE MOLECULAR BASIS OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA: ASSESSMENT IN A LARGE COHORT OF HYPERCHOLESTEROLEMIC CHILDREN

Atherosclerosis. Supplements, 2011-06, Vol.12 (1), p.16-16

2011

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Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps

Energy & environmental science, 2015-06, Vol.8 (6), p.1748-1763

2015

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Abstract: 577 COLESEVELAM ADDED TO STABLE COMBINATION OF STATIN AND EZETIMIBE IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA; THE TRIPLE TRIAL

Atherosclerosis. Supplements, 2009-06, Vol.10 (2), p.e338-e338

2009

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Changes in mineralogical and leaching properties of converter steel slag resulting from accelerated carbonation at low CO2 pressure

Waste management (Elmsford), 2011-11, Vol.31 (11), p.2236-2244

2011

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Characteristics of wheat straw lignins from ethanol-based organosolv treatment

Industrial crops and products, 2014-08, Vol.59, p.85-95

2014

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Biobased alkylphenols from lignins via a two-step pyrolysis – Hydrodeoxygenation approach

Bioresource technology, 2017-04, Vol.229, p.160-168

2017

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Plasma levels of PCSK9 and phenotypic variability in familial hypercholesterolemia

Evaluation of cholesterol lowering treatment of patients with familial hypercholesterolemia: a large cross-sectional study in The Netherlands

Factor VIII deficiency does not protect against atherosclerosis

Venous thrombosis is associated with hyperglycemia at diagnosis: a case–control study

Real-time MSE measurements for current profile control on KSTAR

Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis

Familial hypercholesterolemia patients with unexplained low ldl-c: a role for angptl3?

Statins Reduce Hepatic Angptl3 Expression And Secretion, Likely By Interfering With Lxr-Mediated Transcription

Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes

Hip surgery sequentially induces stress hyperglycaemia and activates coagulation

Colesevelam added to combination therapy with a statin and ezetimibe in patients with familial hypercholesterolemia: A 12-week, multicenter, randomized, double-blind, controlled trial

Real-time MSE measurements for current profile control on KSTARa

Abstract: P870 IDENTIFICATION OF APOB AND PCSK9 MUTATIONS CAUSING A NON-ADH PHENOTYPE IN MOLECULAR DIAGNOSED ADH PATIENTS

P40 CAROTID ATHEROSCLEROSIS OF PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA NO LONGER DIFFERS FROM UNAFFECTED RELATIVES ALREADY WITHIN 18 MONTHS AFTER IDENTIFICATION

L6 EFFICACY OF 15 YEARS OF GENETIC CASCADE SCREENING FOR FAMILIAL HYPERCHOLESTEROLEMIA IN THE NETHERLANDS IN PREVENTION OF CORONARY ARTERY DISEASE

603 COMBINING EXOME SEQUENCING WITH EXCLUSION LINKAGE ANALYSIS AS A TOOL TO UNRAVEL THE MOLECULAR BASIS OF A COMMON GENETIC DISEASE

Abstract: P841 NON-FUNCTIONALITY OF THREE LDL-R AND APOB GENE MUTATIONS THAT WERE ASSUMED TO CAUSE FAMILIAL HYPERCHOLESTEROLEMIA

Abstract: 576 LIPID-LOWERING MEDICATION TWO YEARS AFTER MOLECULAR DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA

MS351 FOLLOW-UP OF CHILDREN AFTER POSITIVE GENETIC TESTING IN THE DUTCH NATIONAL SCREENING PROGRAM FOR FAMILIAL HYPERCHOLESTEROLEMIA

66 THE MOLECULAR BASIS OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA: ASSESSMENT IN A LARGE COHORT OF HYPERCHOLESTEROLEMIC CHILDREN

Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps

Abstract: 577 COLESEVELAM ADDED TO STABLE COMBINATION OF STATIN AND EZETIMIBE IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA; THE TRIPLE TRIAL

Changes in mineralogical and leaching properties of converter steel slag resulting from accelerated carbonation at low CO2 pressure

Characteristics of wheat straw lignins from ethanol-based organosolv treatment

Biobased alkylphenols from lignins via a two-step pyrolysis – Hydrodeoxygenation approach

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