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Patrizia Tarugi

Showing results (31-40 of 78) with videos related to

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Atherosclerosis|June 16, 2007
Molecular diagnosis of hypobetalipoproteinemia: an ENID reviewPatrizia Tarugi, Maurizio Averna, Enza Di Leo, et al.
Atherosclerosis|December 19, 2009
Pseudoxanthoma elasticum and familial hypercholesterolemia: a deleterious combination of cardiovascular risk factorsLivia Pisciotta, Patrizia Tarugi, Claudia Borrini, et al.
Atherosclerosis|April 16, 2011
Plasma non-cholesterol sterols in primary hypobetalipoproteinemiaDavide Noto, Angelo B Cefalù, Giacoma Barraco, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology|May 11, 2016
Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow upMehmet Gündüz, Eda Özaydın, Müge Büyüktaşlı Atar, et al.
Atherosclerosis. Supplements|October 3, 2017
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN)Maurizio Averna, Angelo B Cefalù, Manuela Casula, et al.
Current Vascular Pharmacology|February 21, 2012
Lipid and apoprotein composition of HDL in partial or complete CETP deficiencyEric J Niesor, Elisabeth von der Mark, Laura Calabresi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 28, 2015
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein BBerna Seker Yilmaz, Neslihan Onenli Mungan, Enza Di Leo, 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.
Circulation. Cardiovascular Genetics|July 31, 2015
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein FunctionMeghan T Walsh, Jahangir Iqbal, Joby Josekutty, 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.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Atherosclerosis|June 16, 2007
Molecular diagnosis of hypobetalipoproteinemia: an ENID reviewPatrizia Tarugi, Maurizio Averna, Enza Di Leo, et al.
Atherosclerosis|December 19, 2009
Pseudoxanthoma elasticum and familial hypercholesterolemia: a deleterious combination of cardiovascular risk factorsLivia Pisciotta, Patrizia Tarugi, Claudia Borrini, et al.
Atherosclerosis|April 16, 2011
Plasma non-cholesterol sterols in primary hypobetalipoproteinemiaDavide Noto, Angelo B Cefalù, Giacoma Barraco, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology|May 11, 2016
Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow upMehmet Gündüz, Eda Özaydın, Müge Büyüktaşlı Atar, et al.
Atherosclerosis. Supplements|October 3, 2017
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN)Maurizio Averna, Angelo B Cefalù, Manuela Casula, et al.
Current Vascular Pharmacology|February 21, 2012
Lipid and apoprotein composition of HDL in partial or complete CETP deficiencyEric J Niesor, Elisabeth von der Mark, Laura Calabresi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 28, 2015
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein BBerna Seker Yilmaz, Neslihan Onenli Mungan, Enza Di Leo, 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.
Circulation. Cardiovascular Genetics|July 31, 2015
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein FunctionMeghan T Walsh, Jahangir Iqbal, Joby Josekutty, 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.
Pageof 8