1. Detection of a new mutation in the apoB gene: A case report of a pediatric patient with familial hypobetalipoproteinemia (FHBL). (December 2020) Authors: Koniari, E.; Skouma, A.; Zarkada, I.; Dragoti, A.; Constantoulakis, P.; Samara, S.; Chrousos, G. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e210 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic analysis of a rare form of dyslipidemia: Sitosterolemia in a Greek patient. (December 2020) Authors: Koniari, E.; Skouma, A.; Dragoti, A.; Oikonomaki, K.; Constantoulakis, P.; Chrousos, G. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e210 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Spectrum of LDLR gene mutations, causing familial hypercholesterolemia (FH) in Greece: Un update. (December 2020) Authors: Koniari, E.; Skouma, A.; Dragoti, A.; Garoufi, A.; Maroulis, V.; Papadakis, M.; Chrousos, G. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗