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Sebastiano Calandra

Showing results (41-50 of 88) with videos related to

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Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 6, 2022
Search for familial hypercholesterolemia patients in an Italian community: A real-life retrospective studyTommaso Fasano, Chiara Trenti, Emanuele A Negri, et al.
Seminars in Vascular Medicine|January 5, 2005
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemiaSebastiano Calandra, Stefano Bertolini, Giovanni Mario Pes, et al.
Clinical Medicine Insights. Case Reports|December 19, 2013
Lipoprotein glomerulopathy associated with a mutation in apolipoprotein eRiccardo Magistroni, Marco Bertolotti, Luciana Furci, et al.
Atherosclerosis|February 5, 2013
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in ItalyStefano Bertolini, Livia Pisciotta, Claudio Rabacchi, et al.
Journal of Lipid Research|October 29, 2002
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblastsPatrizia Tarugi, Giorgia Ballarini, Bruno Bembi, et al.
Journal of Clinical Lipidology|October 21, 2019
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemiaClaudio Rabacchi, Maria Luisa Simone, Livia Pisciotta, et al.
The Journal of Pediatrics|May 19, 2009
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemiaOrnella Guardamagna, Gabriella Restagno, Elio Rolfo, et al.
Atherosclerosis|June 24, 2003
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyLivia Pisciotta, Roberto Miccoli, Alfredo Cantafora, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 14, 2004
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemiaClaudio Priore Oliva, Livia Pisciotta, Giovanni Li Volti, et al.
Journal of Clinical Lipidology|December 22, 2015
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)Livia Pisciotta, Cecilia Vitali, Elda Favari, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 6, 2022
Search for familial hypercholesterolemia patients in an Italian community: A real-life retrospective studyTommaso Fasano, Chiara Trenti, Emanuele A Negri, et al.
Seminars in Vascular Medicine|January 5, 2005
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemiaSebastiano Calandra, Stefano Bertolini, Giovanni Mario Pes, et al.
Clinical Medicine Insights. Case Reports|December 19, 2013
Lipoprotein glomerulopathy associated with a mutation in apolipoprotein eRiccardo Magistroni, Marco Bertolotti, Luciana Furci, et al.
Atherosclerosis|February 5, 2013
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in ItalyStefano Bertolini, Livia Pisciotta, Claudio Rabacchi, et al.
Journal of Lipid Research|October 29, 2002
Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblastsPatrizia Tarugi, Giorgia Ballarini, Bruno Bembi, et al.
Journal of Clinical Lipidology|October 21, 2019
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemiaClaudio Rabacchi, Maria Luisa Simone, Livia Pisciotta, et al.
The Journal of Pediatrics|May 19, 2009
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemiaOrnella Guardamagna, Gabriella Restagno, Elio Rolfo, et al.
Atherosclerosis|June 24, 2003
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyLivia Pisciotta, Roberto Miccoli, Alfredo Cantafora, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 14, 2004
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemiaClaudio Priore Oliva, Livia Pisciotta, Giovanni Li Volti, et al.
Journal of Clinical Lipidology|December 22, 2015
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)Livia Pisciotta, Cecilia Vitali, Elda Favari, et al.
Pageof 9