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Journal of the American College of Cardiology
|
March 25, 1992
Lipoprotein cholesterol, apolipoprotein A-I and B and lipoprotein (a) abnormalities in men with premature coronary artery disease
J Genest, J R McNamara, J M Ordovas, et al.
Journal of Steroid Biochemistry
|
May 1, 1975
Dynamic aldosterone and 18-hydroxydeoxycorticosterone studies in labile and stable benign essential hypertension
W Nowaczynski, O Kuchel, J Genest, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 2, 2008
Vascular calcifications in homozygote familial hypercholesterolemia
Z Awan, K Alrasadi, G A Francis, et al.
Atherosclerosis
|
May 11, 1990
DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery disease
J J Genest, J M Ordovas, J R McNamara, et al.
Circulation
|
June 11, 1992
Familial lipoprotein disorders in patients with premature coronary artery disease
J J Genest, S S Martin-Munley, J R McNamara, et al.
QJM : Monthly Journal of the Association of Physicians
|
September 12, 2007
Venous thromboembolism in association with features of the metabolic syndrome
J G Ray, E Lonn, Q Yi, et al.
Circulation
|
March 10, 2001
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
S M Clee, A H Zwinderman, J C Engert, et al.
Paediatric and Perinatal Epidemiology
|
August 25, 2001
Socio-economic disparities in preterm birth: causal pathways and mechanisms
M S Kramer, L Goulet, J Lydon, et al.
The Journal of Clinical Investigation
|
November 22, 2000
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
S M Clee, J J Kastelein, M van Dam, et al.
Lancet (London, England)
|
October 26, 1999
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
M Marcil, A Brooks-Wilson, S M Clee, et al.
Page
of 53
Search research articles
Search
Showing results (511-520 of 521) with videos related to
Sort By:
Page
of 53
Journal of the American College of Cardiology
|
March 25, 1992
Lipoprotein cholesterol, apolipoprotein A-I and B and lipoprotein (a) abnormalities in men with premature coronary artery disease
J Genest, J R McNamara, J M Ordovas, et al.
Journal of Steroid Biochemistry
|
May 1, 1975
Dynamic aldosterone and 18-hydroxydeoxycorticosterone studies in labile and stable benign essential hypertension
W Nowaczynski, O Kuchel, J Genest, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 2, 2008
Vascular calcifications in homozygote familial hypercholesterolemia
Z Awan, K Alrasadi, G A Francis, et al.
Atherosclerosis
|
May 11, 1990
DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery disease
J J Genest, J M Ordovas, J R McNamara, et al.
Circulation
|
June 11, 1992
Familial lipoprotein disorders in patients with premature coronary artery disease
J J Genest, S S Martin-Munley, J R McNamara, et al.
QJM : Monthly Journal of the Association of Physicians
|
September 12, 2007
Venous thromboembolism in association with features of the metabolic syndrome
J G Ray, E Lonn, Q Yi, et al.
Circulation
|
March 10, 2001
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
S M Clee, A H Zwinderman, J C Engert, et al.
Paediatric and Perinatal Epidemiology
|
August 25, 2001
Socio-economic disparities in preterm birth: causal pathways and mechanisms
M S Kramer, L Goulet, J Lydon, et al.
The Journal of Clinical Investigation
|
November 22, 2000
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
S M Clee, J J Kastelein, M van Dam, et al.
Lancet (London, England)
|
October 26, 1999
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
M Marcil, A Brooks-Wilson, S M Clee, et al.
Page
of 53