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Defesche

Showing results (91-100 of 178) with videos related to

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Journal of Applied Genetics|February 12, 2008
Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in the LDLR geneJolanta Kubalska, Magdalena Chmara, Janusz Limon, et al.
Journal of Clinical Lipidology|February 24, 2019
The clinical and molecular diversity of homozygous familial hypercholesterolemia in children: Results from the GeneTics of clinical homozygous hypercholesterolemia (GoTCHA) studyIlse K Luirink, Marjet J A M Braamskamp, Albert Wiegman, et al.
The Netherlands Journal of Medicine|August 4, 2012
APOE1 mutation in a patient with type III hyperlipoproteinaemia: detailed genetic analysis requiredM E Visser, G M Dallinga-Thie, S J Pinto-Sietsma, et al.
Journal of Internal Medicine|January 25, 2003
Prevalence and significance of cardiovascular risk factors in a large cohort of patients with familial hypercholesterolaemiaP R W de Sauvage Nolting, J C Defesche, R J A Buirma, et al.
Journal of Hypertension|February 28, 2008
Haplotype of the angiotensinogen gene is associated with coronary heart disease in familial hypercholesterolemiaJeroen B van der Net, Aaron Isaacs, Geesje M Dallinga-Thie, et al.
European Heart Journal|July 3, 2010
A frequent variant in the ABCA1 gene is associated with increased coronary heart disease risk and a better response to statin treatment in familial hypercholesterolemia patientsJorie Versmissen, Daniëlla M Oosterveer, Mojgan Yazdanpanah, et al.
Circulation. Genomic and Precision Medicine|December 19, 2018
A Deep Intronic Variant in LDLR in Familial HypercholesterolemiaLaurens F Reeskamp, Merel L Hartgers, Jorge Peter, et al.
Human Genetics|December 1, 1993
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch populationJ C Defesche, D E van Diermen, P J Lansberg, et al.
Atherosclerosis|April 14, 2009
5-Lipoxygenase activating protein (ALOX5AP) gene variants associate with the presence of xanthomas in familial hypercholesterolemiaDaniëlla M Oosterveer, Jorie Versmissen, Mojgan Yazdanpanah, et al.
Journal of Clinical Pharmacology|April 1, 1990
Clinical safety of flurbiprofenC D Brooks, O I Linet, D Schellenberg, et al.
Pageof 18

Showing results (91-100 of 178) with videos related to

Sort By:
Pageof 18
Journal of Applied Genetics|February 12, 2008
Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in the LDLR geneJolanta Kubalska, Magdalena Chmara, Janusz Limon, et al.
Journal of Clinical Lipidology|February 24, 2019
The clinical and molecular diversity of homozygous familial hypercholesterolemia in children: Results from the GeneTics of clinical homozygous hypercholesterolemia (GoTCHA) studyIlse K Luirink, Marjet J A M Braamskamp, Albert Wiegman, et al.
The Netherlands Journal of Medicine|August 4, 2012
APOE1 mutation in a patient with type III hyperlipoproteinaemia: detailed genetic analysis requiredM E Visser, G M Dallinga-Thie, S J Pinto-Sietsma, et al.
Journal of Internal Medicine|January 25, 2003
Prevalence and significance of cardiovascular risk factors in a large cohort of patients with familial hypercholesterolaemiaP R W de Sauvage Nolting, J C Defesche, R J A Buirma, et al.
Journal of Hypertension|February 28, 2008
Haplotype of the angiotensinogen gene is associated with coronary heart disease in familial hypercholesterolemiaJeroen B van der Net, Aaron Isaacs, Geesje M Dallinga-Thie, et al.
European Heart Journal|July 3, 2010
A frequent variant in the ABCA1 gene is associated with increased coronary heart disease risk and a better response to statin treatment in familial hypercholesterolemia patientsJorie Versmissen, Daniëlla M Oosterveer, Mojgan Yazdanpanah, et al.
Circulation. Genomic and Precision Medicine|December 19, 2018
A Deep Intronic Variant in LDLR in Familial HypercholesterolemiaLaurens F Reeskamp, Merel L Hartgers, Jorge Peter, et al.
Human Genetics|December 1, 1993
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch populationJ C Defesche, D E van Diermen, P J Lansberg, et al.
Atherosclerosis|April 14, 2009
5-Lipoxygenase activating protein (ALOX5AP) gene variants associate with the presence of xanthomas in familial hypercholesterolemiaDaniëlla M Oosterveer, Jorie Versmissen, Mojgan Yazdanpanah, et al.
Journal of Clinical Pharmacology|April 1, 1990
Clinical safety of flurbiprofenC D Brooks, O I Linet, D Schellenberg, et al.
Pageof 18