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European Heart Journal
|
October 1, 1988
Results of serial coronary angiography in patients with homozygous familial hypercholesterolaemia
J M Klein, G Drobinski, E Bruckert, et al.
The American Journal of Cardiology
|
July 15, 1999
Usefulness in predicting coronary artery disease by ultrasonic evaluation of the carotid arteries in asymptomatic hypercholesterolemic patients with positive exercise stress tests
P Giral, E Bruckert, F Dairou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 31, 1995
Blood antioxidants (vitamin E and beta-carotene) in long-term low density lipoprotein apheresis
U Assogba, S Lepage, E Bruckert, et al.
Lancet (London, England)
|
September 1, 1990
Kaposi's sarcoma and HTLV-I infection
C Veyssier-Belot, L J Couderc, C Desgranges, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 13, 1990
Does electrophoresis reliably screen for high serum lipoprotein Lp(a)?
E Bruckert, J Truffert, J L De Gennes, et al.
Arteriosclerosis (Dallas, Tex.)
|
September 1, 1985
Direct fetal blood examination for prenatal diagnosis of homozygous familial hypercholesterolemia
J L de Gennes, F Daffos, F Dairou, et al.
Atherosclerosis
|
February 1, 1992
Carotid stenosis is a powerful predictor of a positive exercise electrocardiogram in a large hyperlipidemic population
E Bruckert, P Giral, J Salloum, et al.
Haemostasis
|
January 1, 1989
Coagulation factor VII and plasma triglycerides. Decreased catabolism as a possible mechanism of factor VII hyperactivity
J Carvalho de Sousa, E Bruckert, P Giral, et al.
Human Mutation
|
January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method
N Loux, B Saint-Jore, G Collod, et al.
Human Mutation
|
January 1, 1996
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100
P Benlian, J L de Gennes, F Dairou, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
European Heart Journal
|
October 1, 1988
Results of serial coronary angiography in patients with homozygous familial hypercholesterolaemia
J M Klein, G Drobinski, E Bruckert, et al.
The American Journal of Cardiology
|
July 15, 1999
Usefulness in predicting coronary artery disease by ultrasonic evaluation of the carotid arteries in asymptomatic hypercholesterolemic patients with positive exercise stress tests
P Giral, E Bruckert, F Dairou, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 31, 1995
Blood antioxidants (vitamin E and beta-carotene) in long-term low density lipoprotein apheresis
U Assogba, S Lepage, E Bruckert, et al.
Lancet (London, England)
|
September 1, 1990
Kaposi's sarcoma and HTLV-I infection
C Veyssier-Belot, L J Couderc, C Desgranges, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 13, 1990
Does electrophoresis reliably screen for high serum lipoprotein Lp(a)?
E Bruckert, J Truffert, J L De Gennes, et al.
Arteriosclerosis (Dallas, Tex.)
|
September 1, 1985
Direct fetal blood examination for prenatal diagnosis of homozygous familial hypercholesterolemia
J L de Gennes, F Daffos, F Dairou, et al.
Atherosclerosis
|
February 1, 1992
Carotid stenosis is a powerful predictor of a positive exercise electrocardiogram in a large hyperlipidemic population
E Bruckert, P Giral, J Salloum, et al.
Haemostasis
|
January 1, 1989
Coagulation factor VII and plasma triglycerides. Decreased catabolism as a possible mechanism of factor VII hyperactivity
J Carvalho de Sousa, E Bruckert, P Giral, et al.
Human Mutation
|
January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method
N Loux, B Saint-Jore, G Collod, et al.
Human Mutation
|
January 1, 1996
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100
P Benlian, J L de Gennes, F Dairou, et al.
Page
of 5