Showing results (11-20 of 179) with videos related to
Sort By:
Pageof 18
The Journal of Pediatrics|March 20, 1998
The C677T mutation in the methylenetetrahydrofolate reductase gene predisposes to hyperhomocysteinemia in children with familial hypercholesterolemia treated with cholestyramineS Tonstad, H Refsum, L Ose, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Determinants of lipid levels among children with heterozygous familial hypercholesterolemia in NorwayS Tonstad, T P Leren, M Sivertsen, et al.Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 20, 1994
[A comparison between lovastatin and pravastatin--effects on lipids, sleep and quality of life in primary hyperlipidemia]S Tonstad, C Gørbitz, L Ose, et al.The Journal of Pediatrics|July 1, 1996
Efficacy and safety of cholestyramine therapy in peripubertal and prepubertal children with familial hypercholesterolemiaS Tonstad, J Knudtzon, M Sivertsen, et al.Cytometry|August 1, 1995
Standardization of a flow cytometric method for measurement of low-density lipoprotein receptor activity on blood mononuclear cellsK Løhne, P Urdal, T P Leren, et al.Cytometry|December 31, 1997
Flow cytometric measurement of low density lipoprotein receptor activity validated by DNA analysis in diagnosing heterozygous familial hypercholesterolemiaP Urdal, T P Leren, S Tonstad, et al.Human Genetics|August 1, 1995
Two novel point mutations in the EGF precursor homology domain of the LDL receptor gene causing familial hypercholesterolemiaT P Leren, K Solberg, O K Rødningen, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 13, 2002
Serum cholesterol response to replacing butter with a new trans-free margarine in hypercholesterolemic subjectsS Tonstad, E C Strøm, C S Bergei, et al.Human Mutation|July 22, 1998
Effects of a 9.6-kb deletion of the LDL receptor gene (FH Helsinki) on structure and levels of mRNAO K Rødningen, S Tonstad, L Ose, et al.Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1994
Familial hypercholesterolaemia caused by a non-sense mutation in codon 329 of the LDL receptor geneK Solberg, O K Rødningen, S Tonstad, et al.Pageof 18