1. Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report. (August 2022) Authors: De Gier, C.; Skacel, G.; Walleczek, N.-K.; Lischka, J.; Baumgartner, M.; Greber-Platzer, S. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗