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Stefano Bertolini

Showing results (31-40 of 97) with videos related to

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Frontiers in Genetics|July 7, 2022
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 23, 2010
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier diseaseLetizia Bocchi, Livia Pisciotta, Tommaso Fasano, et al.
Atherosclerosis. Supplements|October 3, 2017
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN studyAngela Pirillo, Katia Garlaschelli, Marcello Arca, et al.
Biochimica Et Biophysica Acta|January 21, 2004
Hypobetalipoproteinemia with an apparently recessive inheritance due to a "de novo" mutation of apolipoprotein BSandra Lancellotti, Enza Di Leo, Junia Y Penacchioni, et al.
Atherosclerosis|May 12, 2006
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemiaClaudio Priore Oliva, Patrizia Tarugi, Sebastiano Calandra, et al.
Journal of Clinical Lipidology|August 24, 2022
Plasma HDL pattern, cholesterol efflux and cholesterol loading capacity of serum in carriers of a novel missense variant (Gly176Trp) of endothelial lipaseLivia Pisciotta, Alice Ossoli, Annalisa Ronca, et al.
Atherosclerosis|March 22, 2005
Serum homocysteine, methylenetetrahydrofolate reductase gene polymorphism and cardiovascular disease in heterozygous familial hypercholesterolemiaLivia Pisciotta, Claudio Cortese, Agostino Gnasso, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 29, 2007
Molecular characterization of two patients with severe LCAT deficiencyValentine Charlton-Menys, Livia Pisciotta, Paul N Durrington, et al.
Journal of Clinical Lipidology|February 19, 2013
A silent mutation of Niemann-Pick C1-like 1 and apolipoprotein E4 modulate cholesterol absorption in primary hyperlipidemiasGraziana Lupattelli, Livia Pisciotta, Stefano De Vuono, et al.
Molecular Genetics and Metabolism|March 25, 2009
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA geneLivia Pisciotta, Raffaele Fresa, Antonella Bellocchio, et al.
Pageof 10

Showing results (31-40 of 97) with videos related to

Sort By:
Pageof 10
Frontiers in Genetics|July 7, 2022
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 23, 2010
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier diseaseLetizia Bocchi, Livia Pisciotta, Tommaso Fasano, et al.
Atherosclerosis. Supplements|October 3, 2017
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN studyAngela Pirillo, Katia Garlaschelli, Marcello Arca, et al.
Biochimica Et Biophysica Acta|January 21, 2004
Hypobetalipoproteinemia with an apparently recessive inheritance due to a "de novo" mutation of apolipoprotein BSandra Lancellotti, Enza Di Leo, Junia Y Penacchioni, et al.
Atherosclerosis|May 12, 2006
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemiaClaudio Priore Oliva, Patrizia Tarugi, Sebastiano Calandra, et al.
Journal of Clinical Lipidology|August 24, 2022
Plasma HDL pattern, cholesterol efflux and cholesterol loading capacity of serum in carriers of a novel missense variant (Gly176Trp) of endothelial lipaseLivia Pisciotta, Alice Ossoli, Annalisa Ronca, et al.
Atherosclerosis|March 22, 2005
Serum homocysteine, methylenetetrahydrofolate reductase gene polymorphism and cardiovascular disease in heterozygous familial hypercholesterolemiaLivia Pisciotta, Claudio Cortese, Agostino Gnasso, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 29, 2007
Molecular characterization of two patients with severe LCAT deficiencyValentine Charlton-Menys, Livia Pisciotta, Paul N Durrington, et al.
Journal of Clinical Lipidology|February 19, 2013
A silent mutation of Niemann-Pick C1-like 1 and apolipoprotein E4 modulate cholesterol absorption in primary hyperlipidemiasGraziana Lupattelli, Livia Pisciotta, Stefano De Vuono, et al.
Molecular Genetics and Metabolism|March 25, 2009
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA geneLivia Pisciotta, Raffaele Fresa, Antonella Bellocchio, et al.
Pageof 10