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Stefano Bertolini

Showing results (21-30 of 97) with videos related to

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Gene|February 28, 2002
Functional analysis of the promoter of human sterol 27-hydroxylase gene in HepG2 cellsRita Garuti, Maria Antonietta Croce, Luana Piccinini, et al.
Annali Dell'Istituto Superiore Di Sanita|May 23, 2003
Investigation into the role of apolipoprotein B gene 8344C/T variant on plasma cholesterol levels by allele-specific PCR amplificationAlfredo Cantafora, Stefano Bertolini, Ida Blotta, et al.
Journal of Clinical Lipidology|September 1, 2016
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 geneClaudio Rabacchi, Sergio D'Addato, Silvia Palmisano, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 27, 2009
An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemiaClaudio Rabacchi, Alessia Wunsch, Margherita Ghisellini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2011
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemiaLivia Pisciotta, Raffaele Fresa, Antonella Bellocchio, et al.
Journal of Lipid Research|August 25, 2011
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskSebastiano Calandra, Patrizia Tarugi, Helen E Speedy, et al.
Journal of Clinical Lipidology|September 1, 2016
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutationsClaudio Rabacchi, Federico Bigazzi, Mariarita Puntoni, et al.
Atherosclerosis|October 24, 2007
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemiaLivia Pisciotta, Tommaso Fasano, Laura Calabresi, et al.
Frontiers in Genetics|May 5, 2023
Corrigendum: The role of registers in increasing knowledge and improving management of children and adolescents affected by familial hypercholesterolemia: The LIPIGEN pediatric groupMarta Gazzotti, Manuela Casula, Stefano Bertolini, et al.
JIMD Reports|October 22, 2013
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusionLorenza Pugni, Enrica Riva, Carlo Pietrasanta, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Gene|February 28, 2002
Functional analysis of the promoter of human sterol 27-hydroxylase gene in HepG2 cellsRita Garuti, Maria Antonietta Croce, Luana Piccinini, et al.
Annali Dell'Istituto Superiore Di Sanita|May 23, 2003
Investigation into the role of apolipoprotein B gene 8344C/T variant on plasma cholesterol levels by allele-specific PCR amplificationAlfredo Cantafora, Stefano Bertolini, Ida Blotta, et al.
Journal of Clinical Lipidology|September 1, 2016
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 geneClaudio Rabacchi, Sergio D'Addato, Silvia Palmisano, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 27, 2009
An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemiaClaudio Rabacchi, Alessia Wunsch, Margherita Ghisellini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2011
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemiaLivia Pisciotta, Raffaele Fresa, Antonella Bellocchio, et al.
Journal of Lipid Research|August 25, 2011
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskSebastiano Calandra, Patrizia Tarugi, Helen E Speedy, et al.
Journal of Clinical Lipidology|September 1, 2016
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutationsClaudio Rabacchi, Federico Bigazzi, Mariarita Puntoni, et al.
Atherosclerosis|October 24, 2007
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemiaLivia Pisciotta, Tommaso Fasano, Laura Calabresi, et al.
Frontiers in Genetics|May 5, 2023
Corrigendum: The role of registers in increasing knowledge and improving management of children and adolescents affected by familial hypercholesterolemia: The LIPIGEN pediatric groupMarta Gazzotti, Manuela Casula, Stefano Bertolini, et al.
JIMD Reports|October 22, 2013
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusionLorenza Pugni, Enrica Riva, Carlo Pietrasanta, et al.
Pageof 10