C. Priore Oliva

A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia.

S. Bertolini, C. Priore Oliva, P. Tarugi, 2006, Atherosclerosis.

Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

M. P. Leòn, L. Cortesi, M. Ponz de Leòn, 2014, Techniques in Coloproctology.

Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia.

R. Fresa, D. Noto, A. Cantafora, 2006, Atherosclerosis.

Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia.

R. Fresa, S. Bertolini, C. Priore Oliva, 2011, Clinica chimica acta; international journal of clinical chemistry.

Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparison.

R. Fresa, M. Arca, A. Cantafora, 2006, Atherosclerosis.

APOA5 and triglyceride metabolism, lesson from human APOA5 deficiency.

S. Bertolini, C. Priore Oliva, P. Tarugi, 2006, Current opinion in lipidology.