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The impact of overweight on lipid phenotype in different forms of dyslipidemia: a retrospective cohort study

Journal of endocrinological investigation, 2024-04

2024

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Whey proteins inhibit food intake and tend to improve oxidative balance in obese zucker rats

Eating and weight disorders, 2021-12, Vol.26 (8), p.2453-2461

2021

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A case report of secondary dislipidemia

Nutrition, metabolism, and cardiovascular diseases, 2017-01, Vol.27 (1), p.e23-e24

2017

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Molecular characterization of three Italian cases of lipoprotein glomerulopathy

Atherosclerosis, 2014-08, Vol.235 (2), p.e242-e242

2014

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Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia

Nutrition, metabolism, and cardiovascular diseases, 2012-10, Vol.22 (10), p.831-835

2012

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Evaluation of efficacy and safety of Evolocumab 140 mg in genetically characterized He-FH patients. First experience of Genoa lipid clinic

Nutrition, metabolism, and cardiovascular diseases, 2017-01, Vol.27 (1), p.e10-e10

2017

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Xanthomata striata palmaris regression with fenofibrate in type III dyslipoproteinemia: a clinical report

Nutrition, metabolism, and cardiovascular diseases, 2016-09, Vol.26 (9), p.848-850

2016

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Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations

Nutrition, metabolism, and cardiovascular diseases, 2013-08, Vol.23 (8), p.732-736

2013

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Phenotypic expression and genotype analysis of eleven patients with cholesteryl ester storage disease and identification of a novel lipa gene variant

Nutrition, metabolism, and cardiovascular diseases, 2017-01, Vol.27 (1), p.e32-e32

2017

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[87] PARAMETERS SIGNIFICANTLY ASSOCIATED WITH TENDON XANTHOMATOSIS (Tx) IN 619 GENETICALLY CHARACTERIZED ITALIAN FH PATIENTS

Nutrition, metabolism, and cardiovascular diseases, 2009, Vol.19, p.S22-S22

2009

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Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 gene

European journal of clinical investigation, 2007-12, Vol.37 (12), p.997-1000

2007

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Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia

Atherosclerosis, 2005-06, Vol.180 (2), p.311-318

2005

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Both low and extremely high monogenic HDL-cholesterol states are characterised by defective capacity of HDL to acquire free cholesterol upon triglyceride lipolysis

Atherosclerosis, 2023-08, Vol.379, p.S59

2023

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T06.01.17 STAGING OF LIVER FIBROSIS WITH ULTRASOUND MORPHOLOGICAL HEPATIC FEATURES IN PATIENTS AFFECTED BY HCV HEPATITIS AND NAFLD

Digestive and liver disease, 2020-10, Vol.52, p.S165-S166

2020

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The association between vitamin D and psoriasis: A systematic review with meta-analysis

Clinical nutrition ESPEN, 2023-12, Vol.58, p.633-634

2023

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Severe HDL deficiency due to novel defects in the ABCA1 transporter

Journal of internal medicine, 2009-03, Vol.265 (3), p.359-372

2009

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Observational multicenter study on effectiveness and tolerability of alirocumab in real world, The Omero study: Interim data from the fist 352 participants

Atherosclerosis, 2021-08, Vol.331, p.e166-e166

2021

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Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype

Arteriosclerosis, thrombosis, and vascular biology, 2000-09, Vol.20 (9), p.E41

2000

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P1066 The real-life use of the Crohn's disease exclusion diet (CDED) in adults with mild-to-moderate Crohn's disease activity: an interim analysis of an open-label randomized controlled trial

Journal of Crohn's and colitis, 2024-01, Vol.18 (Supplement_1), p.i1915-i1915

2024

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Long-term follow-up of genetically confirmed patients with familial hypercholesterolemia from the treatment with the first-generation statins to monoclonal anti-PCSK9 antibodies

Atherosclerosis, 2020-12, Vol.315, p.e212-e212

2020

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Role of dietary intervention in patients with metabolic syndrome and NAFLD-NASH

Atherosclerosis, 2020-12, Vol.315, p.e262-e262

2020

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Evaluation of adherence to Mediterranean diet, assessed by a food frequency questionnaire, in dyslipidemic patients and evaluation of dietary intervention efficacy

Atherosclerosis, 2020-12, Vol.315, p.e219-e220

2020

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Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs)

Clinical nephrology, 2008-03, Vol.69 (3), p.213-218

2008

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[93] A NOVEL ITALIAN NONSENSE MUTATION OF LDLR GENE CAUSING SEVERE HYPERCHOLESTEROLEMIA (FH PESCARA)

Nutrition, metabolism, and cardiovascular diseases, 2009, Vol.19, p.S24-S24

2009

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[86] BERBERINE (BBR) 500 mg IS MORE EFFECTIVE THAN EZETIMIBE 10 mg IN REDUCING LDL-CHOLESTEROL IN HYPERCHOLESTEROLEMIC PATIENTS INTOLERANT TO STATINS

Nutrition, metabolism, and cardiovascular diseases, 2009, Vol.19, p.S22-S22

2009

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The impact of overweight on lipid phenotype in different forms of dyslipidemia: a retrospective cohort study

Whey proteins inhibit food intake and tend to improve oxidative balance in obese zucker rats

A case report of secondary dislipidemia

Molecular characterization of three Italian cases of lipoprotein glomerulopathy

Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia

Evaluation of efficacy and safety of Evolocumab 140 mg in genetically characterized He-FH patients. First experience of Genoa lipid clinic

Xanthomata striata palmaris regression with fenofibrate in type III dyslipoproteinemia: a clinical report

Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations

Phenotypic expression and genotype analysis of eleven patients with cholesteryl ester storage disease and identification of a novel lipa gene variant

[87] PARAMETERS SIGNIFICANTLY ASSOCIATED WITH TENDON XANTHOMATOSIS (Tx) IN 619 GENETICALLY CHARACTERIZED ITALIAN FH PATIENTS

Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 gene

Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia

Both low and extremely high monogenic HDL-cholesterol states are characterised by defective capacity of HDL to acquire free cholesterol upon triglyceride lipolysis

T06.01.17 STAGING OF LIVER FIBROSIS WITH ULTRASOUND MORPHOLOGICAL HEPATIC FEATURES IN PATIENTS AFFECTED BY HCV HEPATITIS AND NAFLD

The association between vitamin D and psoriasis: A systematic review with meta-analysis

Severe HDL deficiency due to novel defects in the ABCA1 transporter

Observational multicenter study on effectiveness and tolerability of alirocumab in real world, The Omero study: Interim data from the fist 352 participants

Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype

P1066 The real-life use of the Crohn's disease exclusion diet (CDED) in adults with mild-to-moderate Crohn's disease activity: an interim analysis of an open-label randomized controlled trial

Long-term follow-up of genetically confirmed patients with familial hypercholesterolemia from the treatment with the first-generation statins to monoclonal anti-PCSK9 antibodies

Role of dietary intervention in patients with metabolic syndrome and NAFLD-NASH

Evaluation of adherence to Mediterranean diet, assessed by a food frequency questionnaire, in dyslipidemic patients and evaluation of dietary intervention efficacy

Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs)

[93] A NOVEL ITALIAN NONSENSE MUTATION OF LDLR GENE CAUSING SEVERE HYPERCHOLESTEROLEMIA (FH PESCARA)

[86] BERBERINE (BBR) 500 mg IS MORE EFFECTIVE THAN EZETIMIBE 10 mg IN REDUCING LDL-CHOLESTEROL IN HYPERCHOLESTEROLEMIC PATIENTS INTOLERANT TO STATINS

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