1. Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation. (23rd September 2013) Authors: Sheikhzadeh, S.; Sondermann, C.; Rybczynski, M.; Habermann, C.R.; Brockstaedt, L.; Keyser, B.; Kaemmerer, H.; Mir, T.; Staebler, A.; Robinson, P.N.; Kutsche, K.; Berger, J.; Blankenberg, S.; von Kodolitsch, Y. Journal: Clinical genetics Issue: Volume 86:Number 3(2014:Sep.) Page Start: 238 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Dural ectasia in Loeys–Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation. (17th December 2013) Authors: Sheikhzadeh, S.; Brockstaedt, L.; Habermann, C.R.; Sondermann, C.; Bannas, P.; Mir, T.S.; Staebler, A.; Seidel, H.; Keyser, B.; Arslan‐Kirchner, M.; Kutsche, K.; Berger, J.; Blankenberg, S.; von Kodolitsch, Y. Journal: Clinical genetics Issue: Volume 86:Number 6(2014:Dec.) Page Start: 545 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗