1. Cardiovascular disease in children with homozygous familial hypercholesterolemia. (August 2022) Authors: Lischka, J.; Baumgartner, M.; De Gier, C.; Willfort-Ehringer, A.; Greber-Platzer, S. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. EP25.08: The value of pattern recognition of ultrasound diagnosis of adnexal masses compared to the histological outcome. (September 2017) Authors: De Gier, C.; Koch, M.; Schwab, S.; Bader, Y.T.; Hoeschler, N.; Helmy, S. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 50(2017)Supplement 1 Page Start: 376 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. OC08.04: Local versus systemic methotrexate in uterine ectopic pregnancies. (September 2017) Authors: Schwab, S.; Koch, M.; De Gier, C.; Hoeschler, N.; Bader, Y.T.; Helmy, S. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 50(2017)Supplement 1 Page Start: 15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. OP15.04: Diagnostic performance of IOTA models in adnexal masses: a retrospective assessment. (September 2017) Authors: Hoeschler, N.; Koch, M.; De Gier, C.; Schwab, S.; Bader, Y.T.; Helmy, S. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 50(2017)Supplement 1 Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The correlation of myokines with lipid metabolism and inflammation in youth with severe obesity. (August 2022) Authors: Baumgartner, M.; Lischka, J.; De Gier, C.; Schanzer, A.; Walleczek, N.-K.; Greber-Platzer, S.; Zeyda, M. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 163 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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) ↗