1. Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease. Issue 3 (24th January 2018) Authors: Schormair, B.; Kemlink, D.; Mollenhauer, B.; Fiala, O.; Machetanz, G.; Roth, J.; Berutti, R.; Strom, T.M.; Haslinger, B.; Trenkwalder, C.; Zahorakova, D.; Martasek, P.; Ruzicka, E.; Winkelmann, J. Journal: Clinical genetics Issue: Volume 93:Issue 3(2018) Page Start: 603 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. EFNS/MDS‐ES recommendations for the diagnosis of Parkinson's disease. Issue 1 (22nd December 2012) Authors: Berardelli, A.; Wenning, G. K.; Antonini, A.; Berg, D.; Bloem, B. R.; Bonifati, V.; Brooks, D.; Burn, D. J.; Colosimo, C.; Fanciulli, A.; Ferreira, J.; Gasser, T.; Grandas, F.; Kanovsky, P.; Kostic, V.; Kulisevsky, J.; Oertel, W.; Poewe, W.; Reese, J.‐P.; Relja, M. Journal: European journal of neurology Issue: Volume 20:Issue 1(2013:Jan.) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗