1. Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. (19th July 2017) Authors: Feichtinger, René G.; Brunner-Krainz, Michaela; Alhaddad, Bader; Wortmann, Saskia B.; Kovacs-Nagy, Reka; Stojakovic, Tatjana; Erwa, Wolfgang; Resch, Bernhard; Windischhofer, Werner; Verheyen, Sarah; Uhrig, Sabine; Windpassinger, Christian; Locker, Felix; Makowski, Christine; Strom, Tim M.; Meitin... Other Names: Hüttemann Maik Academic Editor. Journal: Oxidative medicine and cellular longevity Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. HLA genotyping as first-line screening tool for coeliac disease in children with juvenile idiopathic arthritis. Issue 7 (23rd February 2017) Authors: Skrabl-Baumgartner, Andrea; Christine Hauer, Almuthe; Erwa, Wolfgang; Jahnel, Jörg Journal: Archives of disease in childhood Issue: Volume 102:Issue 7(2017) Page Start: 607 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Reply. Issue 1 (19th June 2015) Authors: Krones, Elisabeth; Erwa, Wolfgang; Trauner, Michael; Fickert, Peter Journal: Hepatology Issue: Volume 63:Issue 1(2016:Jan.) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Serum alkaline phosphatase levels accurately reflect cholestasis in mice. Issue 3 (19th June 2015) Authors: Krones, Elisabeth; Erwa, Wolfgang; Trauner, Michael; Fickert, Peter Journal: Hepatology Issue: Volume 62:Issue 3(2015:Sep.) Page Start: 981 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗