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Showing results (121-130 of 144) with videos related to

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Clinical Genetics|February 1, 1996
Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemiaK E Gundersen, K Solberg, O K Rødningen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1996
Risk factors related to carotid intima-media thickness and plaque in children with familial hypercholesterolemia and control subjectsS Tonstad, O Joakimsen, E Stensland-Bugge, et al.
Journal of Lipid Research|January 1, 1997
Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass LpA-IT P Leren, K S Bakken, U Daum, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 9, 2006
Increased levels of C-reactive protein and interleukin-6 in hyperhomocysteinemic subjectsK B Holven, P Aukrust, K Retterstol, et al.
American Journal of Medical Genetics|May 9, 2001
Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine beta-synthase deficiency: relationship between genotype and phenotypeA B Guttormsen, P M Ueland, W D Kruger, et al.
Clinical and Experimental Pharmacology & Physiology|September 1, 1976
Circulating dopamine-beta-hydroxylase (DbetaH) and catecholamines in a paediatric phaeochromocytomaK B Helle, G Serck-Hanssen, O Sövik, et al.
Journal of Internal Medicine|March 1, 1997
Molecular genetics of familial hypercholesterolaemia in NorwayT P Leren, S Tonstad, K E Gundersen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1997
[Application of gene technology in the diagnosis of familial hypercholesterolemia]T P Leren, K S Bakken, O K Rødningen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 1, 1995
A novel variant of lysosomal acid lipase (Leu336-->Pro) associated with acid lipase deficiency and cholesterol ester storage diseaseU Seedorf, H Wiebusch, S Muntoni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 7, 2005
Altered composition of HDL3 in FH subjects causing a HDL subfraction with less atheroprotective functionT R Balstad, K B Holven, I O Ottestad, et al.
Pageof 15

Showing results (121-130 of 144) with videos related to

Sort By:
Pageof 15
Clinical Genetics|February 1, 1996
Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemiaK E Gundersen, K Solberg, O K Rødningen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1996
Risk factors related to carotid intima-media thickness and plaque in children with familial hypercholesterolemia and control subjectsS Tonstad, O Joakimsen, E Stensland-Bugge, et al.
Journal of Lipid Research|January 1, 1997
Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass LpA-IT P Leren, K S Bakken, U Daum, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 9, 2006
Increased levels of C-reactive protein and interleukin-6 in hyperhomocysteinemic subjectsK B Holven, P Aukrust, K Retterstol, et al.
American Journal of Medical Genetics|May 9, 2001
Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine beta-synthase deficiency: relationship between genotype and phenotypeA B Guttormsen, P M Ueland, W D Kruger, et al.
Clinical and Experimental Pharmacology & Physiology|September 1, 1976
Circulating dopamine-beta-hydroxylase (DbetaH) and catecholamines in a paediatric phaeochromocytomaK B Helle, G Serck-Hanssen, O Sövik, et al.
Journal of Internal Medicine|March 1, 1997
Molecular genetics of familial hypercholesterolaemia in NorwayT P Leren, S Tonstad, K E Gundersen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1997
[Application of gene technology in the diagnosis of familial hypercholesterolemia]T P Leren, K S Bakken, O K Rødningen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 1, 1995
A novel variant of lysosomal acid lipase (Leu336-->Pro) associated with acid lipase deficiency and cholesterol ester storage diseaseU Seedorf, H Wiebusch, S Muntoni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 7, 2005
Altered composition of HDL3 in FH subjects causing a HDL subfraction with less atheroprotective functionT R Balstad, K B Holven, I O Ottestad, et al.
Pageof 15