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Showing results (121-130 of 178) with videos related to

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Clinical Genetics|September 27, 2000
Low-density lipoprotein receptor gene mutations in a Southeast Asian population with familial hypercholesterolemiaK L Khoo, P van Acker, J C Defesche, et al.
Journal of Clinical Medicine|February 25, 2023
The Effect of Bimanual Intensive Functional Training on Somatosensory Hand Function in Children with Unilateral Spastic Cerebral Palsy: An Observational StudyCatherine V M Steinbusch, Anke Defesche, Bertie van der Leij, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 10, 2005
Genetic determinants of cardiovascular disease risk in familial hypercholesterolemiaAngelique C M Jansen, Emily S van Aalst-Cohen, Michael W T Tanck, et al.
Clinical Chemistry|March 1, 1994
Screening for familial defective apolipoprotein B-100 with improved U937 monocyte proliferation assayA J Van den Broek, L Hollaar, H I Schaefer, et al.
Journal of Clinical Lipidology|February 4, 2018
Alirocumab efficacy in patients with double heterozygous, compound heterozygous, or homozygous familial hypercholesterolemiaMerel L Hartgers, Joep C Defesche, Gisle Langslet, et al.
European Heart Journal|January 18, 2013
Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoproteinVincenzo Sorrentino, Sigrid W Fouchier, Mohammad M Motazacker, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 1, 1995
Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemiaS N Pimstone, S E Gagné, C Gagné, et al.
Atherosclerosis|February 10, 2006
The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patientsR Durst, A Jansen, G Erez, et al.
Annals of Internal Medicine|May 7, 2008
Familial defective apolipoprotein B and familial hypobetalipoproteinemia in one family: two neutralizing mutationsAnouk van der Graaf, Sigrid W Fouchier, Maud N Vissers, et al.
Pageof 18

Showing results (121-130 of 178) with videos related to

Sort By:
Pageof 18
Clinical Genetics|September 27, 2000
Low-density lipoprotein receptor gene mutations in a Southeast Asian population with familial hypercholesterolemiaK L Khoo, P van Acker, J C Defesche, et al.
Journal of Clinical Medicine|February 25, 2023
The Effect of Bimanual Intensive Functional Training on Somatosensory Hand Function in Children with Unilateral Spastic Cerebral Palsy: An Observational StudyCatherine V M Steinbusch, Anke Defesche, Bertie van der Leij, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 10, 2005
Genetic determinants of cardiovascular disease risk in familial hypercholesterolemiaAngelique C M Jansen, Emily S van Aalst-Cohen, Michael W T Tanck, et al.
Clinical Chemistry|March 1, 1994
Screening for familial defective apolipoprotein B-100 with improved U937 monocyte proliferation assayA J Van den Broek, L Hollaar, H I Schaefer, et al.
Journal of Clinical Lipidology|February 4, 2018
Alirocumab efficacy in patients with double heterozygous, compound heterozygous, or homozygous familial hypercholesterolemiaMerel L Hartgers, Joep C Defesche, Gisle Langslet, et al.
European Heart Journal|January 18, 2013
Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoproteinVincenzo Sorrentino, Sigrid W Fouchier, Mohammad M Motazacker, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 1, 1995
Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemiaS N Pimstone, S E Gagné, C Gagné, et al.
Atherosclerosis|February 10, 2006
The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patientsR Durst, A Jansen, G Erez, et al.
Annals of Internal Medicine|May 7, 2008
Familial defective apolipoprotein B and familial hypobetalipoproteinemia in one family: two neutralizing mutationsAnouk van der Graaf, Sigrid W Fouchier, Maud N Vissers, et al.
Pageof 18