1. 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) ↗
2. Refining the dermatological spectrum in primary immunodeficiency: mucosa‐associated lymphoid tissue lymphoma translocation protein 1 deficiency mimicking Netherton/Omenn syndromes. (1st January 2020) 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) ↗
3. A new case of UDP‐galactose transporter deficiency (SLC35A2‐CDG): molecular basis, clinical phenotype, and therapeutic approach. Issue 5 (17th March 2015) Authors: Dörre, K.; Olczak, M.; Wada, Y.; Sosicka, P.; Grüneberg, M.; Reunert, J.; Kurlemann, G.; Fiedler, B.; Biskup, S.; Hörtnagel, K.; Rust, S.; Marquardt, T. Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 5(2015) Page Start: 931 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗