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Sebastiano Calandra

Showing results (21-30 of 88) with videos related to

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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.
Biochimica Et Biophysica Acta|January 31, 2016
Characterization of a mutant form of human apolipoprotein B (Thr26_Tyr27del) associated with familial hypobetalipoproteinemiaLucia Magnolo, Davide Noto, Angelo B Cefalù, 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.
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.
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.
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.
Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2003
Adult onset Niemann-Pick type C disease: A clinical, neuroimaging and molecular genetic studyCarla Battisti, Patrizla Tarugi, Maria Teresa Dotti, 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.
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.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
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.
Biochimica Et Biophysica Acta|January 31, 2016
Characterization of a mutant form of human apolipoprotein B (Thr26_Tyr27del) associated with familial hypobetalipoproteinemiaLucia Magnolo, Davide Noto, Angelo B Cefalù, 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.
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.
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.
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.
Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2003
Adult onset Niemann-Pick type C disease: A clinical, neuroimaging and molecular genetic studyCarla Battisti, Patrizla Tarugi, Maria Teresa Dotti, 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.
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.
Pageof 9