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Sebastiano Calandra

Showing results (71-80 of 88) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 2025
Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN RegistryLaura D'Erasmo, Daniele Tramontano, Alessia Di Costanzo, et al.
Lancet (London, England)|March 19, 2002
Autosomal recessive hypercholesterolaemia in Sardinia, Italy, and mutations in ARH: a clinical and molecular genetic analysisMarcello Arca, Giovanni Zuliani, Kenneth Wilund, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 13, 2024
Consensus document on diagnosis and management of familial hypercholesterolemia from the Italian Society for the Study of Atherosclerosis (SISA)Patrizia Tarugi, Stefano Bertolini, Sebastiano Calandra, et al.
Circulation. Cardiovascular Genetics|November 9, 2011
Characterization of three kindreds with familial combined hypolipidemia caused by loss-of-function mutations of ANGPTL3Livia Pisciotta, Elda Favari, Lucia Magnolo, et al.
Neurogenetics|March 3, 2009
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutationsTatiana Fancello, Andrea Dardis, Camillo Rosano, et al.
Genes|June 28, 2023
Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian FamilyPaola Concolino, Elisa De Paolis, Simona Moffa, et al.
Atherosclerosis|March 17, 2004
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disordersLivia Pisciotta, Ian Hamilton-Craig, Patrizia Tarugi, et al.
Atherosclerosis|May 13, 2022
Lipoprotein(a) and family history for cardiovascular disease in paediatric patients: A new frontier in cardiovascular risk stratification. Data from the LIPIGEN paediatric groupCristina Pederiva, Maria Elena Capra, Giacomo Biasucci, et al.
Atherosclerosis|September 8, 2017
Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variantsLivia Pisciotta, Giulia Tozzi, Lorena Travaglini, et al.
Circulation|August 19, 2009
Functional lecithin: cholesterol acyltransferase is not required for efficient atheroprotection in humansLaura Calabresi, Damiano Baldassarre, Samuela Castelnuovo, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 2025
Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN RegistryLaura D'Erasmo, Daniele Tramontano, Alessia Di Costanzo, et al.
Lancet (London, England)|March 19, 2002
Autosomal recessive hypercholesterolaemia in Sardinia, Italy, and mutations in ARH: a clinical and molecular genetic analysisMarcello Arca, Giovanni Zuliani, Kenneth Wilund, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 13, 2024
Consensus document on diagnosis and management of familial hypercholesterolemia from the Italian Society for the Study of Atherosclerosis (SISA)Patrizia Tarugi, Stefano Bertolini, Sebastiano Calandra, et al.
Circulation. Cardiovascular Genetics|November 9, 2011
Characterization of three kindreds with familial combined hypolipidemia caused by loss-of-function mutations of ANGPTL3Livia Pisciotta, Elda Favari, Lucia Magnolo, et al.
Neurogenetics|March 3, 2009
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutationsTatiana Fancello, Andrea Dardis, Camillo Rosano, et al.
Genes|June 28, 2023
Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian FamilyPaola Concolino, Elisa De Paolis, Simona Moffa, et al.
Atherosclerosis|March 17, 2004
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disordersLivia Pisciotta, Ian Hamilton-Craig, Patrizia Tarugi, et al.
Atherosclerosis|May 13, 2022
Lipoprotein(a) and family history for cardiovascular disease in paediatric patients: A new frontier in cardiovascular risk stratification. Data from the LIPIGEN paediatric groupCristina Pederiva, Maria Elena Capra, Giacomo Biasucci, et al.
Atherosclerosis|September 8, 2017
Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variantsLivia Pisciotta, Giulia Tozzi, Lorena Travaglini, et al.
Circulation|August 19, 2009
Functional lecithin: cholesterol acyltransferase is not required for efficient atheroprotection in humansLaura Calabresi, Damiano Baldassarre, Samuela Castelnuovo, et al.
Pageof 9