Search Results - "Cefalu, Angelo Baldassare"

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    The Atrial Natriuretic Peptide Genetic Variant rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population by CANNONE, Valentina, BALDASSARE CEFALU, Angelo, NOTO, Davide, SCOTT, Christopher G, BAILEY, Kent R, CAVERA, Giovanni, PAGANO, Michele, SAPIENZA, Michelangelo, AVERNA, Maurizio R, BURNETT, John C

    Published in Diabetes care (01-09-2013)
    “…We hypothesized that the minor allele of the atrial natriuretic peptide (ANP) genetic variant rs5068 is associated with a favorable cardiometabolic phenotype…”
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    Journal Article
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    Lipoprotein Abnormalities in Chronic Kidney Disease and Renal Transplantation by Barbagallo, Carlo Maria, Cefalù, Angelo Baldassare, Giammanco, Antonina, Noto, Davide, Caldarella, Rosalia, Ciaccio, Marcello, Averna, Maurizio Rocco, Nardi, Emilio

    Published in Life (Basel, Switzerland) (05-04-2021)
    “…Chronic kidney disease (CKD) is one of the most important risk factors for cardiovascular disease (CVD). Despite the kidney having no direct implications for…”
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    Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases by Giammanco, Antonina, Noto, Davide, Barbagallo, Carlo Maria, Nardi, Emilio, Caldarella, Rosalia, Ciaccio, Marcello, Averna, Maurizio Rocco, Cefalù, Angelo Baldassare

    Published in Life (Basel, Switzerland) (18-06-2021)
    “…Hyperalphalipoproteinemia (HALP) is a lipid disorder characterized by elevated plasma high-density lipoprotein cholesterol (HDL-C) levels above the 90th…”
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    Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles by Norata, Giuseppe Danilo, Garlaschelli, Katia, Grigore, Liliana, Raselli, Sara, Tramontana, Simona, Meneghetti, Fiorella, Artali, Roberto, Noto, Davide, Cefalù, Angelo Baldassare, Buccianti, Gherardo, Averna, Maurizio, Catapano, Alberico Luigi

    Published in Atherosclerosis (01-01-2010)
    “…Abstract Background PCSK9 plays a key role in plasma cholesterol metabolism by modulating the expression of LDL receptors. Objective and methods In this study…”
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    Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia by Pisciotta, Livia, Oliva, Claudio Priore, Cefalù, Angelo Baldassare, Noto, Davide, Bellocchio, Antonella, Fresa, Raffaele, Cantafora, Alfredo, Patel, Dilip, Averna, Maurizio, Tarugi, Patrizia, Calandra, Sebastiano, Bertolini, Stefano

    Published in Atherosclerosis (01-06-2006)
    “…Patients homozygous or compound heterozygous for LDLR mutations or double heterozygous for LDLR and apo B R3500Q mutation have higher LDL-C levels, more…”
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    Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up by Gündüz, Mehmet, Özaydın, Eda, Atar, Müge Büyüktaşlı, Koç, Nevra, Kırsaçlıoğlu, Ceyda, Köse, Gülşen, Cefalù, Angelo Baldassare, Averna, Maurizio, Tarugi, Patrizia

    Published in Indian journal of gastroenterology (01-05-2016)
    “…Abetalipoproteinemia (ABL; OMIM 200100) is a rare autosomal recessive disease that affects the absorption of dietary fats and fat soluble vitamins. Here, we…”
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    Efficacy and safety of lomitapide in homozygous familial hypercholesterolaemia: the pan-European retrospective observational study by D'Erasmo, Laura, Steward, Kim, Cefalù, Angelo Baldassare, Di Costanzo, Alessia, Boersma, Eric, Bini, Simone, Arca, Marcello, van Lennep, Jeanine Roeters

    Published in European journal of preventive cardiology (05-05-2022)
    “…Lomitapide is a lipid-lowering agent indicated as an adjunct therapy for adult homozygous familial hypercholesterolaemia (HoFH). This study evaluated the…”
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    Journal Article
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