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Lancet (London, England)
|
February 24, 2001
Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands
M A Umans-Eckenhausen, J C Defesche, E J Sijbrands, et al.
The Journal of Clinical Investigation
|
January 1, 1997
Tetrahydrobiopterin restores endothelial function in hypercholesterolemia
E Stroes, J Kastelein, F Cosentino, et al.
Human Molecular Genetics
|
April 1, 1993
The apolipoprotein(a) kringle IV repeats which differ from the major repeat kringle are present in variably-sized isoforms
Y Y van der Hoek, M E Wittekoek, U Beisiegel, et al.
The American Journal of Cardiology
|
February 15, 1995
Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability
S J Bredie, T W de Bruin, P N Demacker, et al.
Clinical Drug Investigation
|
August 13, 2016
Efficacy of Concentrated n-3 Fatty Acids in Hypertriglyceridaemia : A Comparison with Gemfibrozil
M van Dam, A F Stalenhoef, J Wittekoek, et al.
The American Journal of Medicine
|
November 10, 2015
2013 Cholesterol Guidelines Revisited: Percent LDL Cholesterol Reduction or Attained LDL Cholesterol Level or Both for Prognosis?
Sripal Bangalore, Rana Fayyad, John J Kastelein, et al.
Atherosclerosis
|
September 16, 1999
Familial hypercholesterolemia. Acceptor splice site (G-->C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R(Honduras-1) [LDL-R1061(-1) G-->C]
L Yu, E Heere-Ress, B Boucher, et al.
The Journal of Clinical Investigation
|
July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)
J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Clinical Drug Investigation
|
January 15, 2013
Rationale, Design and Baseline Characteristics of a Clinical Trial Comparing the Effects of Robust vs Conventional Cholesterol Lowering and Intima Media Thickness in Patients with Familial Hypercholesterolaemia : The Atorvastatin versus Simvastatin on Atherosclerosis Progression (ASAP) Study
T J Smilde, M D Trip, H Wollersheim, et al.
Archives of Internal Medicine
|
October 25, 1993
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia
J C Defesche, K L Pricker, M R Hayden, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 184) with videos related to
Sort By:
Page
of 19
Lancet (London, England)
|
February 24, 2001
Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands
M A Umans-Eckenhausen, J C Defesche, E J Sijbrands, et al.
The Journal of Clinical Investigation
|
January 1, 1997
Tetrahydrobiopterin restores endothelial function in hypercholesterolemia
E Stroes, J Kastelein, F Cosentino, et al.
Human Molecular Genetics
|
April 1, 1993
The apolipoprotein(a) kringle IV repeats which differ from the major repeat kringle are present in variably-sized isoforms
Y Y van der Hoek, M E Wittekoek, U Beisiegel, et al.
The American Journal of Cardiology
|
February 15, 1995
Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability
S J Bredie, T W de Bruin, P N Demacker, et al.
Clinical Drug Investigation
|
August 13, 2016
Efficacy of Concentrated n-3 Fatty Acids in Hypertriglyceridaemia : A Comparison with Gemfibrozil
M van Dam, A F Stalenhoef, J Wittekoek, et al.
The American Journal of Medicine
|
November 10, 2015
2013 Cholesterol Guidelines Revisited: Percent LDL Cholesterol Reduction or Attained LDL Cholesterol Level or Both for Prognosis?
Sripal Bangalore, Rana Fayyad, John J Kastelein, et al.
Atherosclerosis
|
September 16, 1999
Familial hypercholesterolemia. Acceptor splice site (G-->C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R(Honduras-1) [LDL-R1061(-1) G-->C]
L Yu, E Heere-Ress, B Boucher, et al.
The Journal of Clinical Investigation
|
July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)
J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Clinical Drug Investigation
|
January 15, 2013
Rationale, Design and Baseline Characteristics of a Clinical Trial Comparing the Effects of Robust vs Conventional Cholesterol Lowering and Intima Media Thickness in Patients with Familial Hypercholesterolaemia : The Atorvastatin versus Simvastatin on Atherosclerosis Progression (ASAP) Study
T J Smilde, M D Trip, H Wollersheim, et al.
Archives of Internal Medicine
|
October 25, 1993
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia
J C Defesche, K L Pricker, M R Hayden, et al.
Page
of 19