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 (11-20 of 78) with videos related to

Pageof 8
Sort By:
Journal of Hepatology|May 17, 2005
Pediatric gallstone disease in familial hypobetalipoproteinemiaSandra Lancellotti, Marco Zaffanello, Enza Di Leo, et al.
Biochimica Et Biophysica Acta|August 4, 2016
Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjectsMeghan T Walsh, Enza Di Leo, Ilyas Okur, et al.
Atherosclerosis|September 25, 2020
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular featuresStefano Bertolini, Sebastiano Calandra, Marcello Arca, et al.
Human Mutation|October 2, 2004
A point mutation in the lariat branch point of intron 6 of NPC1 as the cause of abnormal pre-mRNA splicing in Niemann-Pick type C diseaseEnza Di Leo, Francesca Panico, Patrizia Tarugi, et al.
Journal of Clinical Lipidology|March 28, 2025
Clinical and biochemical spectrum of APOB-related hypobetalipoproteinemia: Insights from a retrospective cohort studyİlknur Sürücü Kara, Engin Köse, Hatice Mutlu, et al.
Journal of Clinical Lipidology|September 1, 2016
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 geneClaudio Rabacchi, Sergio D'Addato, Silvia Palmisano, et al.
Journal of Lipid Research|August 25, 2011
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskSebastiano Calandra, Patrizia Tarugi, Helen E Speedy, et al.
Acta Diabetologica|November 3, 2016
Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol-diabetes connection? A systematic review of literatureDavide Noto, Marcello Arca, Patrizia Tarugi, 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.
Journal of Clinical Lipidology|June 16, 2015
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncationsEnza Di Leo, Tuba Eminoglu, Lucia Magnolo, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
Journal of Hepatology|May 17, 2005
Pediatric gallstone disease in familial hypobetalipoproteinemiaSandra Lancellotti, Marco Zaffanello, Enza Di Leo, et al.
Biochimica Et Biophysica Acta|August 4, 2016
Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjectsMeghan T Walsh, Enza Di Leo, Ilyas Okur, et al.
Atherosclerosis|September 25, 2020
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular featuresStefano Bertolini, Sebastiano Calandra, Marcello Arca, et al.
Human Mutation|October 2, 2004
A point mutation in the lariat branch point of intron 6 of NPC1 as the cause of abnormal pre-mRNA splicing in Niemann-Pick type C diseaseEnza Di Leo, Francesca Panico, Patrizia Tarugi, et al.
Journal of Clinical Lipidology|March 28, 2025
Clinical and biochemical spectrum of APOB-related hypobetalipoproteinemia: Insights from a retrospective cohort studyİlknur Sürücü Kara, Engin Köse, Hatice Mutlu, et al.
Journal of Clinical Lipidology|September 1, 2016
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 geneClaudio Rabacchi, Sergio D'Addato, Silvia Palmisano, et al.
Journal of Lipid Research|August 25, 2011
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskSebastiano Calandra, Patrizia Tarugi, Helen E Speedy, et al.
Acta Diabetologica|November 3, 2016
Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol-diabetes connection? A systematic review of literatureDavide Noto, Marcello Arca, Patrizia Tarugi, 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.
Journal of Clinical Lipidology|June 16, 2015
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncationsEnza Di Leo, Tuba Eminoglu, Lucia Magnolo, et al.
Pageof 8