Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Circulation. Cardiovascular Genetics|June 7, 2011
Assessment of carotid atherosclerosis in normocholesterolemic individuals with proven mutations in the low-density lipoprotein receptor or apolipoprotein B genesRoeland Huijgen, Maud N Vissers, Iris Kindt, et al.
Human Mutation|May 28, 2010
Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemiaRoeland Huijgen, Iris Kindt, Sigrid W Fouchier, et al.
Atherosclerosis|October 2, 2018
LDL-cholesterol target achievement in patients with heterozygous familial hypercholesterolemia at Groote Schuur Hospital: Minority at target despite large reductions in LDL-CXander M van Delden, Roeland Huijgen, Karen H Wolmarans, et al.
Cholesterol|August 13, 2013
Quality assessment of the genetic test for familial hypercholesterolemia in the NetherlandsIris Kindt, Roeland Huijgen, Marieke Boekel, et al.
Journal of Lipid Research|July 9, 2013
Inheritance pattern of familial hypercholesterolemia and markers of cardiovascular riskD Meeike Kusters, Hans J Avis, Marjet J Braamskamp, et al.
Plos One|February 20, 2010
Two years after molecular diagnosis of familial hypercholesterolemia: majority on cholesterol-lowering treatment but a minority reaches treatment goalRoeland Huijgen, Iris Kindt, Sjoerd B J Verhoeven, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|November 6, 2020
Interpretation of laboratory results after gastric bypass surgery: the effects of weight loss and time on 30 blood tests in a 5-year follow-up programArnold W J M van de Laar, Victor E A Gerdes, Roeland Huijgen, et al.
European Journal of Human Genetics : EJHG|February 2, 2012
Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire studyRoeland Huijgen, Sietske J M Homsma, Barbara A Hutten, et al.
Human Mutation|November 19, 2011
Genetic variation in APOB, PCSK9, and ANGPTL3 in carriers of pathogenic autosomal dominant hypercholesterolemic mutations with unexpected low LDL-Cl LevelsRoeland Huijgen, Barbara Sjouke, Kelly Vis, et al.
Atherosclerosis|July 31, 2024
LDLR variant classification for improved cardiovascular risk prediction in familial hypercholesterolemiaShirin Ibrahim, Merel L Hartgers, Laurens F Reeskamp, et al.
Pageof 4