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Clinical Genetics
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February 1, 1996
Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemia
K 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 subjects
S 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-I
T 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 subjects
K 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 phenotype
A 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 phaeochromocytoma
K B Helle, G Serck-Hanssen, O Sövik, et al.
Journal of Internal Medicine
|
March 1, 1997
Molecular genetics of familial hypercholesterolaemia in Norway
T 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 disease
U 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 function
T R Balstad, K B Holven, I O Ottestad, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 144) with videos related to
Sort By:
Page
of 15
Clinical Genetics
|
February 1, 1996
Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemia
K 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 subjects
S 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-I
T 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 subjects
K 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 phenotype
A 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 phaeochromocytoma
K B Helle, G Serck-Hanssen, O Sövik, et al.
Journal of Internal Medicine
|
March 1, 1997
Molecular genetics of familial hypercholesterolaemia in Norway
T 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 disease
U 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 function
T R Balstad, K B Holven, I O Ottestad, et al.
Page
of 15