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Clinical Chemistry
|
June 25, 2005
Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene
Filomena Campagna, Francesca Fioretti, Marco Burattin, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 2, 2008
C242T polymorphism of NADPH oxidase p22phox and recurrence of cardiovascular events in coronary artery disease
Marcello Arca, Beatrice Conti, Anna Montali, et al.
Atherosclerosis
|
October 17, 2022
ANGPTL3 deficiency associates with the expansion of regulatory T cells with reduced lipid content
Alessandra Pinzon Grimaldos, Ilenia Pacella, Simone Bini, et al.
Journal of the American Heart Association
|
October 18, 2023
Real-World Effectiveness of PCSK9 Inhibitors in Reducing LDL-C in Patients With Familial Hypercholesterolemia in Italy: A Retrospective Cohort Study Based on the AIFA Monitoring Registries
Marcello Arca, Simone Celant, Pier Paolo Olimpieri, et al.
Heart Failure Clinics
|
November 15, 2021
New Frontiers in the Treatment of Homozygous Familial Hypercholesterolemia
Arturo Cesaro, Fabio Fimiani, Felice Gragnano, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
October 13, 2005
99mTc-interleukin-2 scintigraphy for the in vivo imaging of vulnerable atherosclerotic plaques
Alessio Annovazzi, Elena Bonanno, Marcello Arca, et al.
Journal of Clinical Lipidology
|
June 11, 2025
Lomitapide-induced fatty liver is a reversible condition: Evidence from a case of familial chylomicronemia syndrome
Daniele Tramontano, Michele di Martino, Francesco Baratta, et al.
Heart (British Cardiac Society)
|
March 15, 2022
Lipoprotein(a): a risk factor for atherosclerosis and an emerging therapeutic target
Stefania Angela Di Fusco, Marcello Arca, Pietro Scicchitano, et al.
Cardiovascular Therapeutics
|
January 24, 2020
Lipid Lowering Treatment and Eligibility for PCSK9 Inhibition in Post-Myocardial Infarction Patients in Italy: Insights from Two Contemporary Nationwide Registries
Furio Colivicchi, Michele Massimo Gulizia, Marcello Arca, et al.
Frontiers in Neurology
|
November 18, 2016
A Novel Mutation in <i>ABCA1</i> Gene Causing Tangier Disease in an Italian Family with Uncommon Neurological Presentation
Marco Ceccanti, Chiara Cambieri, Vittorio Frasca, et al.
Page
of 22
Search research articles
Search
Showing results (91-100 of 212) with videos related to
Sort By:
Page
of 22
Clinical Chemistry
|
June 25, 2005
Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene
Filomena Campagna, Francesca Fioretti, Marco Burattin, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 2, 2008
C242T polymorphism of NADPH oxidase p22phox and recurrence of cardiovascular events in coronary artery disease
Marcello Arca, Beatrice Conti, Anna Montali, et al.
Atherosclerosis
|
October 17, 2022
ANGPTL3 deficiency associates with the expansion of regulatory T cells with reduced lipid content
Alessandra Pinzon Grimaldos, Ilenia Pacella, Simone Bini, et al.
Journal of the American Heart Association
|
October 18, 2023
Real-World Effectiveness of PCSK9 Inhibitors in Reducing LDL-C in Patients With Familial Hypercholesterolemia in Italy: A Retrospective Cohort Study Based on the AIFA Monitoring Registries
Marcello Arca, Simone Celant, Pier Paolo Olimpieri, et al.
Heart Failure Clinics
|
November 15, 2021
New Frontiers in the Treatment of Homozygous Familial Hypercholesterolemia
Arturo Cesaro, Fabio Fimiani, Felice Gragnano, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
October 13, 2005
99mTc-interleukin-2 scintigraphy for the in vivo imaging of vulnerable atherosclerotic plaques
Alessio Annovazzi, Elena Bonanno, Marcello Arca, et al.
Journal of Clinical Lipidology
|
June 11, 2025
Lomitapide-induced fatty liver is a reversible condition: Evidence from a case of familial chylomicronemia syndrome
Daniele Tramontano, Michele di Martino, Francesco Baratta, et al.
Heart (British Cardiac Society)
|
March 15, 2022
Lipoprotein(a): a risk factor for atherosclerosis and an emerging therapeutic target
Stefania Angela Di Fusco, Marcello Arca, Pietro Scicchitano, et al.
Cardiovascular Therapeutics
|
January 24, 2020
Lipid Lowering Treatment and Eligibility for PCSK9 Inhibition in Post-Myocardial Infarction Patients in Italy: Insights from Two Contemporary Nationwide Registries
Furio Colivicchi, Michele Massimo Gulizia, Marcello Arca, et al.
Frontiers in Neurology
|
November 18, 2016
A Novel Mutation in <i>ABCA1</i> Gene Causing Tangier Disease in an Italian Family with Uncommon Neurological Presentation
Marco Ceccanti, Chiara Cambieri, Vittorio Frasca, et al.
Page
of 22