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4. Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population. Issue 1 (February 2015)

6. Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia. (29th August 2020)

7. Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia. (July 2017)

10. Identification and in vitro characterization of two new PCSK9 Gain of Function variants found in patients with Familial Hypercholesterolemia. Issue 1 (December 2017)