1. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (5th June 2019) Authors: Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (June 2019) Authors: Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. P1719Validity of DAPT score to predict late ischemic and hemorrhagic events in patients with ST-segment-elevation acute coronary syndrome. (28th August 2018) Authors: Ferreira Gonzalez, I; Ribera, A R; Marsal, J R; Faixedas, M; Rosas, A; Tizon-Marcos, H T; Rojas, S; Labata, C; Cardenas, M; Homs, S; Tomas-Querol, C; Garcia-Picart, J; Roura, G; Masotti, M; Mauri, J Journal: European heart journal Issue: Volume 39(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗