1. A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis. (16th November 2015) Authors: Lolas, I.B.; Sommerlund, M.; Okkels, H.; Ramsing, M.; Petersen, M.B. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 30:Number 11(2016:Nov.) Page Start: e144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Antifibrotic effect after low‐dose imatinib mesylate treatment in patients with nephrogenic systemic fibrosis: an open‐label non‐randomized, uncontrolled clinical trial. (20th December 2011) Authors: Elmholdt, T.R.; Buus, N.H.; Ramsing, M.; Olesen, A.B. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 27:Number 6(2013:Jun.) Page Start: 779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. New and recurrent AAGAB mutations in punctate palmoplantar keratoderma. (1st August 2014) Authors: Pohler, E.; Huber, M.; Boonen, S.E.; Zamiri, M.; Gregersen, P.A.; Sommerlund, M.; Ramsing, M.; Hohl, D.; McLean, W.H.I.; Smith, F.J.D. Journal: British journal of dermatology Issue: Volume 171:Number 2(2014:Aug.) Page Start: 433 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. New and recurrent AAGAB mutations in punctate palmoplantar keratoderma. (7th August 2014) Authors: Pohler, E.; Huber, M.; Boonen, S.E.; Zamiri, M.; Gregersen, P.A.; Sommerlund, M.; Ramsing, M.; Hohl, D.; McLean, W.H.I.; Smith, F.J.D. Journal: British journal of dermatology Issue: Volume 171:Number 2(2014:Aug.) Page Start: 433 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies. Issue 4 (23rd February 2018) Authors: Rasmussen, M.; Sunde, L.; Nielsen, M.L.; Ramsing, M.; Petersen, A.; Hjortshøj, T.D.; Olsen, T.E.; Tabor, A.; Hertz, J.M.; Johnsen, I.; Sperling, L.; Petersen, O.B.; Jensen, U.B.; Møller, F.G.; Petersen, M.B.; Lildballe, D.L. Journal: Clinical genetics Issue: Volume 93:Issue 4(2018) Page Start: 860 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗