1. A novel missense variant in CREB3L3 gene associated with severe hypertriglyceridemia. (August 2022) Authors: Cardiero, G.; Palma, D.; Di Taranto, M.D.; Esposito, M.V.; Iannuzzo, G.; Di Minno, M.N.D.; Molino, C.; Iannuzzi, A.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 140 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Evidence of novel APO B gene complex allele causing familial hypercholesterolaemia. (August 2022) Authors: Palma, D.; Cardiero, G.; Flagiello, C.; Galicia-Garcia, U.; Larrea, A.; Di Taranto, M.D.; Martin, C.; Iannuzzo, G.; Di Minno, M.N.D.; Pipolo, A.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetics and biochemical profile of patients with homozygous familial hypercholesterolemia. (December 2020) Authors: Di Taranto, M.D.; Giacobbe, C.; Buonaiuto, A.; Calcaterra, I.; Palma, D.; Maione, G.; Cardiero, G.; Iannuzzo, G.; Di Minno, M.N.D.; Rubba, P.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e207 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Identification of a rare variants in ABCG5/ABCG8 genes in patients with clinical suspect of familial hyperchoelsterolemia. (August 2021) Authors: Giacobbe, C.; Di Taranto, M.D.; Palma, D.; Gelzo, M.; Caputo, M.; Cardiero, G.; Corso, G.; Guardamagna, O.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 331(2021) Page Start: e50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. In vitro characterization revealed five new potential pathogenic variants in the APOB gene. (August 2021) Authors: Di Taranto, M.D.; Galicia, U.; Larrea, A.; Giacobbe, C.; Calcaterra, I.; Palma, D.; Cardiero, G.; Iannuzzo, G.; Di Minno, M.N.D.; Iannuzzi, A.; Martín, C.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 331(2021) Page Start: e183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Spectrum of genetic variants in patients suffering from familial chylomicronaemia syndrome and multifactorial chylomicronaemia syndrome. (December 2020) Authors: Giacobbe, C.; Di Taranto, M.D.; Palma, D.; Maione, G.; Cardiero, G.; Forte, F.; Iannuzzo, G.; Rubba, P.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗