1. Expanding the clinical spectrum of the 'HDAC8‐phenotype' – implications for molecular diagnostics, counseling and risk prediction. Issue 5 (25th January 2016) Authors: Parenti, I.; Gervasini, C.; Pozojevic, J.; Wendt, K.S.; Watrin, E.; Azzollini, J.; Braunholz, D.; Buiting, K.; Cereda, A.; Engels, H.; Garavelli, L.; Glazar, R.; Graffmann, B.; Larizza, L.; Lüdecke, H.J.; Mariani, M.; Masciadri, M.; Pié, J.; Ramos, F.J.; Russo, S. Journal: Clinical genetics Issue: Volume 89:Issue 5(2016) Page Start: 564 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Sleep in Mowat-Wilson syndrome (MWS): Clinical and polysomnografic study. (June 2017) Authors: Ricci, E.; Di Pisa, V.; Provini, F.; Ubertiello, S.; Bonetti, S.; Ivanovski, I.; Caraffi, S.; Bascelli, E.; Franzoni, E.; Garavelli, L.; Cordelli, D.M. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e55 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗