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J Kastelein

Showing results (31-40 of 184) with videos related to

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Atherosclerosis|December 24, 1998
The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosisB J Verhoeff, M D Trip, M H Prins, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1991
[A patient with the homozygote form of familial hypercholesterolemia]J W Gorter, P P Schilte, P J Lansberg, et al.
Journal of Clinical Lipidology|September 1, 2016
Pediatric experience with mipomersen as adjunctive therapy for homozygous familial hypercholesterolemiaFrederick J Raal, Marjet J Braamskamp, Sheryl L Selvey, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 18, 1999
[Tracing of patients with familial hypercholesterolemia in the Netherlands]M A Umans-Eckenhausen, J C Defesche, R L Scheerder, et al.
The Netherlands Journal of Medicine|February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemiaJ C Defesche, P J Lansberg, P W Reymer, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|March 1, 1994
Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100A F Stalenhoef, J C Defesche, H A Kleinveld, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 10, 2000
[Higher prevalence of familial hypercholesterolemia than expected in adult patients of four family practices in Netherlands]P J Lansberg, S Tuzgöl, M A van de Ree, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|November 1, 1994
Binding of recombinant apolipoprotein(a) to extracellular matrix proteinsY Y van der Hoek, W Sangrar, G P Côté, et al.
Current Opinion in Lipidology|April 29, 2000
Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiencyM R Hayden, S M Clee, A Brooks-Wilson, et al.
Human Genetics|March 1, 1994
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.
Pageof 19

Showing results (31-40 of 184) with videos related to

Sort By:
Pageof 19
Atherosclerosis|December 24, 1998
The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosisB J Verhoeff, M D Trip, M H Prins, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1991
[A patient with the homozygote form of familial hypercholesterolemia]J W Gorter, P P Schilte, P J Lansberg, et al.
Journal of Clinical Lipidology|September 1, 2016
Pediatric experience with mipomersen as adjunctive therapy for homozygous familial hypercholesterolemiaFrederick J Raal, Marjet J Braamskamp, Sheryl L Selvey, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 18, 1999
[Tracing of patients with familial hypercholesterolemia in the Netherlands]M A Umans-Eckenhausen, J C Defesche, R L Scheerder, et al.
The Netherlands Journal of Medicine|February 1, 1993
Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemiaJ C Defesche, P J Lansberg, P W Reymer, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|March 1, 1994
Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100A F Stalenhoef, J C Defesche, H A Kleinveld, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 10, 2000
[Higher prevalence of familial hypercholesterolemia than expected in adult patients of four family practices in Netherlands]P J Lansberg, S Tuzgöl, M A van de Ree, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|November 1, 1994
Binding of recombinant apolipoprotein(a) to extracellular matrix proteinsY Y van der Hoek, W Sangrar, G P Côté, et al.
Current Opinion in Lipidology|April 29, 2000
Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiencyM R Hayden, S M Clee, A Brooks-Wilson, et al.
Human Genetics|March 1, 1994
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.
Pageof 19