1. Analysis of dominant and recessive parkinsonism genes in REM sleep behavior disorder. (October 2020) Authors: Mufti, K.; Rudakou, U.; Yu, E.; Ruskey, J.A.; Asavesh, F.; Laurent, S.B.; Arnulf, I.; Hu, M.T.M.; Dauvilliers, Y.; Högl, B.; Stefani, A.; Holzknecht, E.; Monaca, C.C.; Abril, B.; Plazzi, G.; Antelmi, E.; Ferini-Strambi, L.; Heidbreder, A.; Young, P.; De Cock, V. Cochen Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. GBA variants in REM sleep behavior disorder risk and conversion: a multicenter study. (October 2020) Authors: Krohn, L.; Ruskey, J.A.; Rudakou, U.; Leveille, E.; Asayesh, F.; Hu, M.T.M.; Arnulf, I.; Dauvilliers, Y.; Högl, B.; Stefani, A.; Monaca, C.C.; Abril, B.; Plazzi, G.; Antelmi, E.; Ferini-Strambi, L.; Heidbreder, A.; Boeve, B.F.; Espay, A.J.; Cochen de Cock, V.; Mollenhauer, B. Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Supplement 1 Page Start: e26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy. Issue 9 (9th September 2017) Authors: Obeso, J.A.; Stamelou, M.; Goetz, C.G.; Poewe, W.; Lang, A.E.; Weintraub, D.; Burn, D.; Halliday, G.M.; Bezard, E.; Przedborski, S.; Lehericy, S.; Brooks, D.J.; Rothwell, J.C.; Hallett, M.; DeLong, M.R.; Marras, C.; Tanner, C.M.; Ross, G.W.; Langston, J.W.; Klein, C. Journal: Movement disorders Issue: Volume 32:Issue 9(2017) Page Start: 1264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy. Issue 9 (September 2017) Authors: Obeso, J.A.; Stamelou, M.; Goetz, C.G.; Poewe, W.; Lang, A.E.; Weintraub, D.; Burn, D.; Halliday, G.M.; Bezard, E.; Przedborski, S.; Lehericy, S.; Brooks, D.J.; Rothwell, J.C.; Hallett, M.; DeLong, M.R.; Marras, C.; Tanner, C.M.; Ross, G.W.; Langston, J.W.; Klein, C. Journal: Movement disorders Issue: Volume 32:Issue 9(2017) Page Start: 1264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies. Issue 3 (16th July 2018) Authors: Ruskey, J.A.; Zhou, S.; Santiago, R.; Franche, L.‐A.; Alam, A.; Roncière, L.; Spiegelman, D.; Fon, E.A.; Trempe, J.‐F.; Kalia, L.V.; Postuma, R.B.; Dupre, N.; Rivard, G.‐E.; Assouline, S.; Amato, D.; Gan‐Or, Z. Journal: Clinical genetics Issue: Volume 94:Issue 3/4(2018) Page Start: 339 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗