Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrizia Tarugi

Showing results (61-70 of 78) with videos related to

Pageof 8
Sort By:
Journal of Clinical Lipidology|July 23, 2017
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemiaAlessia Di Costanzo, Enza Di Leo, Davide Noto, et al.
The Journal of Biological Chemistry|September 10, 2015
Microsomal Triglyceride Transfer Protein Transfers and Determines Plasma Concentrations of Ceramide and Sphingomyelin but Not GlycosylceramideJahangir Iqbal, Meghan T Walsh, Samar M Hammad, et al.
Journal of Clinical Lipidology|May 19, 2022
Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjectsAngelo B Cefalù, Rossella Spina, Davide Noto, 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.
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.
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.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 19, 2009
PCSK9 dominant negative mutant results in increased LDL catabolic rate and familial hypobetalipoproteinemiaBertrand Cariou, Khadija Ouguerram, Yassine Zaïr, 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|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.
The Journal of Clinical Endocrinology and Metabolism|October 13, 2009
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemiaAngelo B Cefalù, Davide Noto, Maria Luisa Arpi, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Journal of Clinical Lipidology|July 23, 2017
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemiaAlessia Di Costanzo, Enza Di Leo, Davide Noto, et al.
The Journal of Biological Chemistry|September 10, 2015
Microsomal Triglyceride Transfer Protein Transfers and Determines Plasma Concentrations of Ceramide and Sphingomyelin but Not GlycosylceramideJahangir Iqbal, Meghan T Walsh, Samar M Hammad, et al.
Journal of Clinical Lipidology|May 19, 2022
Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjectsAngelo B Cefalù, Rossella Spina, Davide Noto, 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.
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.
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.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 19, 2009
PCSK9 dominant negative mutant results in increased LDL catabolic rate and familial hypobetalipoproteinemiaBertrand Cariou, Khadija Ouguerram, Yassine Zaïr, 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|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.
The Journal of Clinical Endocrinology and Metabolism|October 13, 2009
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemiaAngelo B Cefalù, Davide Noto, Maria Luisa Arpi, et al.
Pageof 8