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M Pocovi

Showing results (21-30 of 38) with videos related to

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Diabetologia|January 15, 2004
SNP3 polymorphism in apo A-V gene is associated with small dense LDL particles in Type 2 diabetesE Esteve, E Faure, F Calvo, et al.
Blood Cells, Molecules & Diseases|August 26, 2014
Iron homeostasis and infIammatory biomarker analysis in patients with type 1 Gaucher diseaseB Medrano-Engay, P Irun, J Gervas-Arruga, et al.
Journal of Inherited Metabolic Disease|September 13, 2012
Greater risk of parkinsonism associated with non-N370S GBA1 mutationsM J Barrett, P Giraldo, J L Capablo, et al.
Atherosclerosis|February 1, 1992
The MspI restriction fragment length polymorphism 3' to the apolipoprotein A-II gene: relationships with lipids, apolipoproteins, and premature coronary artery diseaseF Civeira, J Genest, M Pocovi, et al.
Journal of Medical Genetics|April 5, 2005
High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descentS W Fouchier, R R Sankatsing, J Peter, et al.
Thrombosis and Haemostasis|July 10, 1998
Polymorphism of the platelet glycoprotein IIIa gene in patients with coronary stenosisM Garcia-Ribes, D Gonzalez-Lamuño, R Hernandez-Estefania, et al.
Human Mutation|November 21, 2002
A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular diseaseS Castillo, G Reyes, D Tejedor, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 9, 1999
Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white populationS Acton, D Osgood, M Donoghue, et al.
Atherosclerosis|March 11, 1991
Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus. Relationships with lipids, apolipoproteins, and premature coronary artery diseaseJ M Ordovas, F Civeira, J Genest, et al.
Molecular Genetics and Genomics : MGG|April 30, 2010
Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor geneM T Tejedor, A Cenarro, D Tejedor, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Diabetologia|January 15, 2004
SNP3 polymorphism in apo A-V gene is associated with small dense LDL particles in Type 2 diabetesE Esteve, E Faure, F Calvo, et al.
Blood Cells, Molecules & Diseases|August 26, 2014
Iron homeostasis and infIammatory biomarker analysis in patients with type 1 Gaucher diseaseB Medrano-Engay, P Irun, J Gervas-Arruga, et al.
Journal of Inherited Metabolic Disease|September 13, 2012
Greater risk of parkinsonism associated with non-N370S GBA1 mutationsM J Barrett, P Giraldo, J L Capablo, et al.
Atherosclerosis|February 1, 1992
The MspI restriction fragment length polymorphism 3' to the apolipoprotein A-II gene: relationships with lipids, apolipoproteins, and premature coronary artery diseaseF Civeira, J Genest, M Pocovi, et al.
Journal of Medical Genetics|April 5, 2005
High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descentS W Fouchier, R R Sankatsing, J Peter, et al.
Thrombosis and Haemostasis|July 10, 1998
Polymorphism of the platelet glycoprotein IIIa gene in patients with coronary stenosisM Garcia-Ribes, D Gonzalez-Lamuño, R Hernandez-Estefania, et al.
Human Mutation|November 21, 2002
A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular diseaseS Castillo, G Reyes, D Tejedor, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 9, 1999
Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white populationS Acton, D Osgood, M Donoghue, et al.
Atherosclerosis|March 11, 1991
Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus. Relationships with lipids, apolipoproteins, and premature coronary artery diseaseJ M Ordovas, F Civeira, J Genest, et al.
Molecular Genetics and Genomics : MGG|April 30, 2010
Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor geneM T Tejedor, A Cenarro, D Tejedor, et al.
Pageof 4