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S Bertolini

Showing results (151-160 of 166) with videos related to

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Human Mutation|May 25, 1999
Rapid screening of the LDL receptor point mutation FH-Genoa/Palermo. Mutation in brief no. 238. OnlineG Marino, S Travali, T Reyes, et al.
Nephron|June 26, 2001
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutationsA Sessa, G Battini, M Meroni, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 22, 2003
Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second alleleM Rolleri, N Vivona, G Emmanuele, et al.
Science (New York, N.Y.)|April 28, 2001
Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor proteinC K Garcia, K Wilund, M Arca, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Preventive Veterinary Medicine|April 15, 2018
Using multi-criteria risk ranking methodology to select case studies for a generic risk assessment framework for exotic disease incursion and spread through EuropeV Horigan, M De Nardi, R R L Simons, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Transboundary and Emerging Diseases|March 5, 2014
Mosquito surveillance in northwestern Italy to monitor the occurrence of tropical vector-borne diseasesA Pautasso, R Desiato, S Bertolini, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 12, 2002
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemiaA B Cefalù, G Emmanuele, G Marino, et al.
Pageof 17

Showing results (151-160 of 166) with videos related to

Sort By:
Pageof 17
Human Mutation|May 25, 1999
Rapid screening of the LDL receptor point mutation FH-Genoa/Palermo. Mutation in brief no. 238. OnlineG Marino, S Travali, T Reyes, et al.
Nephron|June 26, 2001
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutationsA Sessa, G Battini, M Meroni, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 22, 2003
Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second alleleM Rolleri, N Vivona, G Emmanuele, et al.
Science (New York, N.Y.)|April 28, 2001
Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor proteinC K Garcia, K Wilund, M Arca, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Preventive Veterinary Medicine|April 15, 2018
Using multi-criteria risk ranking methodology to select case studies for a generic risk assessment framework for exotic disease incursion and spread through EuropeV Horigan, M De Nardi, R R L Simons, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Transboundary and Emerging Diseases|March 5, 2014
Mosquito surveillance in northwestern Italy to monitor the occurrence of tropical vector-borne diseasesA Pautasso, R Desiato, S Bertolini, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2000
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotypeS Bertolini, A Cantafora, M Averna, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 12, 2002
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemiaA B Cefalù, G Emmanuele, G Marino, et al.
Pageof 17