1. Correlation between different LDL-R mutations and response to AB-PCSK9 therapy in a group of patient with genetic diagnosis of familial hypercholesterolemia. (December 2020) Authors: Buonaiuto, A.; Gentile, M.; Calcaterra, I.; Giacobbe, C.; Tripaldella, M.; Forte, F.; Di Minno, M.N.D.; Iannuzzo, G.; Fortunato, G.; Rubba, P. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Elucidating the CO2 adsorption mechanisms in the triangular channels of the bis(pyrazolate) MOF Fe2(BPEB)3 by in situ synchrotron X-ray diffraction and molecular dynamics simulations. Issue 32 (1st August 2017) Authors: Giacobbe, C.; Lavigna, E.; Maspero, A.; Galli, S. Journal: Journal of materials chemistry Issue: Volume 5:Issue 32(2017) Page Start: 16964 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. Heterozygous familial hypercholesterolemia (HeFH) in children: an Italian experience. (September 2016) Authors: Guaraldi, F.; Di Taranto, M.D.; Giacobbe, C.; Fortunato, G.; Guardamagna, O. Journal: Atherosclerosis Issue: Volume 252(2016) Page Start: e38 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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) ↗
6. 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) ↗
7. Mirnome study and functional characterization of LDLR: An integrated approach to identify pathogenicity mechanisms in familial hypercholesterolemia patients without causative mutations. (August 2018) Authors: Di taranto, M.D.; Giacobbe, C.; Scotto di Frega, A.; Cordella, A.; Giurato, G.; Rubba, P.; Weisz, A.; Fortunato, G. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: e23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗