1. Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA. (18th March 2015) Authors: Moosbrugger‐Martinz, V.; Jalili, A.; Schossig, A.S.; Jahn‐Bassler, K.; Zschocke, J.; Schmuth, M.; Stingl, G.; Eckl, K.M.; Hennies, H.C.; Gruber, R. Journal: British journal of dermatology Issue: Volume 172:Number 6(2015:Jun.) Page Start: 1628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA. (18th March 2015) Authors: Moosbrugger‐Martinz, V.; Jalili, A.; Schossig, A.S.; Jahn‐Bassler, K.; Zschocke, J.; Schmuth, M.; Stingl, G.; Eckl, K.M.; Hennies, H.C.; Gruber, R. Journal: British journal of dermatology Issue: Volume 172:Number 6(2015:Jun.) Page Start: 1628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA. (1st June 2015) Authors: Moosbrugger‐Martinz, V.; Jalili, A.; Schossig, A.S.; Jahn‐Bassler, K.; Zschocke, J.; Schmuth, M.; Stingl, G.; Eckl, K.M.; Hennies, H.C.; Gruber, R. Journal: British journal of dermatology Issue: Volume 172:Number 6(2015:Jun.) Page Start: 1628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations. (17th January 2017) Authors: Gruber, R.; Rainer, G.; Weiss, A.; Udvardi, A.; Thiele, H.; Eckl, K.M.; Schupart, R.; Nürnberg, P.; Zschocke, J.; Schmuth, M.; Volc‐Platzer, B.; Hennies, H.C. Journal: British journal of dermatology Issue: Volume 176:Number 4(2017) Page Start: 1068 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations. (1st April 2017) Authors: Gruber, R.; Rainer, G.; Weiss, A.; Udvardi, A.; Thiele, H.; Eckl, K.M.; Schupart, R.; Nürnberg, P.; Zschocke, J.; Schmuth, M.; Volc‐Platzer, B.; Hennies, H.C. Journal: British journal of dermatology Issue: Volume 176:Number 4(2017) Page Start: 1068 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis. (13th January 2022) Authors: Hake, L.; Süßmuth, K.; Komlosi, K.; Kopp, J.; Drerup, C.; Metze, D.; Traupe, H.; Hausser, I.; Eckl, K.M.; Hennies, H.C.; Fischer, J.; Oji, V. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 4(2022) Page Start: 582 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Update: advanced methods in three‐dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders. (1st December 2014) Authors: Eckl, K.M. Journal: British journal of dermatology Issue: Volume 171:Number 6(2014:Dec.) Page Start: 1289 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Update: advanced methods in three‐dimensional organotypic tissue engineering for congenital ichthyosis and other rare keratinization disorders. (December 2014) Authors: Eckl, K.M. Journal: British journal of dermatology Issue: Volume 171:Number 6(2014:Dec.) Page Start: 1289 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗