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Sigrid W Fouchier

Showing results (1-10 of 21) with videos related to

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Current Opinion in Lipidology|May 9, 2013
Lysosomal acid lipase A and the hypercholesterolaemic phenotypeSigrid W Fouchier, Joep C Defesche
Journal of Medical Genetics|November 22, 2014
Current novel-gene-finding strategy for autosomal-dominant hypercholesterolaemia needs refinementSigrid W Fouchier, Barbara A Hutten, Joep C Defesche
Human Mutation|October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The NetherlandsSigrid W Fouchier, John J P Kastelein, Joep C Defesche
Journal of the American College of Cardiology|May 17, 2005
What promise does PCSK9 hold?John J P Kastelein, Sigrid W Fouchier, Joep C Defesche
European Journal of Human Genetics : EJHG|September 29, 2005
Management of hereditary dyslipidaemia; the paradigm of autosomal dominant hypercholesterolaemiaSigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Seminars in Vascular Medicine|January 5, 2005
Familial defective apolipoprotein B versus familial hypercholesterolemia: an assessment of riskSigrid W Fouchier, Joep C Defesche, John J P Kastelein, et al.
Atherosclerosis|July 18, 2016
Sequencing for LIPA mutations in patients with a clinical diagnosis of familial hypercholesterolemiaBarbara Sjouke, Joep C Defesche, Janine S E de Randamie, 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.
Circulation Research|July 19, 2014
Mutations in STAP1 are associated with autosomal dominant hypercholesterolemiaSigrid W Fouchier, Geesje M Dallinga-Thie, Joost C M Meijers, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 9, 2005
Hepatic and cardiovascular consequences of familial hypobetalipoproteinemiaRaaj R Sankatsing, Sigrid W Fouchier, Stefan de Haan, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Current Opinion in Lipidology|May 9, 2013
Lysosomal acid lipase A and the hypercholesterolaemic phenotypeSigrid W Fouchier, Joep C Defesche
Journal of Medical Genetics|November 22, 2014
Current novel-gene-finding strategy for autosomal-dominant hypercholesterolaemia needs refinementSigrid W Fouchier, Barbara A Hutten, Joep C Defesche
Human Mutation|October 27, 2005
Update of the molecular basis of familial hypercholesterolemia in The NetherlandsSigrid W Fouchier, John J P Kastelein, Joep C Defesche
Journal of the American College of Cardiology|May 17, 2005
What promise does PCSK9 hold?John J P Kastelein, Sigrid W Fouchier, Joep C Defesche
European Journal of Human Genetics : EJHG|September 29, 2005
Management of hereditary dyslipidaemia; the paradigm of autosomal dominant hypercholesterolaemiaSigrid W Fouchier, Jessica Rodenburg, Joep C Defesche, et al.
Seminars in Vascular Medicine|January 5, 2005
Familial defective apolipoprotein B versus familial hypercholesterolemia: an assessment of riskSigrid W Fouchier, Joep C Defesche, John J P Kastelein, et al.
Atherosclerosis|July 18, 2016
Sequencing for LIPA mutations in patients with a clinical diagnosis of familial hypercholesterolemiaBarbara Sjouke, Joep C Defesche, Janine S E de Randamie, 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.
Circulation Research|July 19, 2014
Mutations in STAP1 are associated with autosomal dominant hypercholesterolemiaSigrid W Fouchier, Geesje M Dallinga-Thie, Joost C M Meijers, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 9, 2005
Hepatic and cardiovascular consequences of familial hypobetalipoproteinemiaRaaj R Sankatsing, Sigrid W Fouchier, Stefan de Haan, et al.
Pageof 3