1. Association of Cole disease with novel heterozygous mutations in the somatomedin‐B domains of the ENPP1 gene: necessary, but not always sufficient. (18th February 2016) Authors: Schlipf, N.A.; Traupe, H.; Gilaberte, Y.; Peitsch, W.K.; Hausser, I.; Oji, V.; Schmieder, A.; Schneider, S.W.; Demmer, P.; Rösler, B.; Fischer, J. Journal: British journal of dermatology Issue: Volume 174:Number 5(2016) Page Start: 1152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association analysis of psoriasis vulgaris and psoriatic arthritis with loss‐of‐function mutations in IL36RN in German patients. (24th July 2016) Authors: Löhr, S.; Uebe, S.; Behrens, F.; Böhm, B.; Köhm, M.; Traupe, H.; Oji, V.; Burkhardt, H.; Reis, A.; Hüffmeier, U. Journal: British journal of dermatology Issue: Volume 175:Number 3(2016) Page Start: 639 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Management of congenital ichthyoses: European guidelines of care, part one. (3rd December 2018) Authors: Mazereeuw‐Hautier, J.; Vahlquist, A.; Traupe, H.; Bygum, A.; Amaro, C.; Aldwin, M.; Audouze, A.; Bodemer, C.; Bourrat, E.; Diociaiuti, A.; Dolenc‐Voljc, M.; Dreyfus, I.; El Hachem, M.; Fischer, J.; Gånemo, A.; Gouveia, C.; Gruber, R.; Hadj‐Rabia, S.; Hohl, D.; Jonca, N. Journal: British journal of dermatology Issue: Volume 180:Number 2(2019) Page Start: 272 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Refining the dermatological spectrum in primary immunodeficiency: mucosa‐associated lymphoid tissue lymphoma translocation protein 1 deficiency mimicking Netherton/Omenn syndromes. (21st July 2019) Authors: Wiegmann, H.; Reunert, J.; Metze, D.; Marquardt, T.; Engel, T.; Kunde, V.; Ehl, S.; Foell, D.; van den Heuvel, I.; Oji, V.; Wittkowski, H. Journal: British journal of dermatology Issue: Volume 182:Number 1(2020) Page Start: 202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Development of a pathogenesis‐based therapy for peeling skin syndrome type 1. (2nd November 2020) Authors: Valentin, F.; Wiegmann, H.; Tarinski, T.; Nikolenko, H.; Traupe, H.; Liebau, E.; Dathe, M.; Oji, V. Journal: British journal of dermatology Issue: Volume 184:Number 6(2021) Page Start: 1123 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma. (15th March 2022) Authors: Cuperus, E.; Bygum, A.; Boeckmann, L.; Bodemer, C.; Bolling, M.C.; Caproni, M.; Diociaiuti, A.; Emmert, S.; Fischer, J.; Gostynski, A.; Guez, S.; van Gijn, M.E.; Hannulla‐Jouppi, K.; Has, C.; Hernández‐Martín, A.; Martinez, A.E.; Mazereeuw‐Hautier, J.; Medvecz, M.; Neri, I.; Sigurdsson, V. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 7(2022) Page Start: 973 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 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) ↗
8. Association analysis of psoriasis vulgaris and psoriatic arthritis with loss‐of‐function mutations in IL36RN in German patients. (1st September 2016) Authors: Löhr, S.; Uebe, S.; Behrens, F.; Böhm, B.; Köhm, M.; Traupe, H.; Oji, V.; Burkhardt, H.; Reis, A.; Hüffmeier, U. Journal: British journal of dermatology Issue: Volume 175:Number 3(2016) Page Start: 639 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Association of Cole disease with novel heterozygous mutations in the somatomedin‐B domains of the ENPP1 gene: necessary, but not always sufficient. (1st May 2016) Authors: Schlipf, N.A.; Traupe, H.; Gilaberte, Y.; Peitsch, W.K.; Hausser, I.; Oji, V.; Schmieder, A.; Schneider, S.W.; Demmer, P.; Rösler, B.; Fischer, J. Journal: British journal of dermatology Issue: Volume 174:Number 5(2016) Page Start: 1152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. LEKTI domains D6, D7 and D8+9 serve as substrates for transglutaminase 1: implications for targeted therapy of Netherton syndrome. (1st November 2019) Authors: Wiegmann, H.; Valentin, F.; Tarinski, T.; Liebau, E.; Loser, K.; Traupe, H.; Oji, V. Journal: British journal of dermatology Issue: Volume 181:Number 5(2019) Page Start: 999 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗