1. DEEP PHENOTYPING OF THE G2019S LRRK2 MUTATION IN PARKINSON'S DISEASE: UCL COHORT. Issue 12 (15th November 2016) Authors: Rizig, Mie; Jonvik, Hallgeir; Foltynie, Thomas; Limousin, Patricia; Bhatia, Kailash; Warner, Thomas; Morris, Huw; Wood, Nicholas Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87:Issue 12(2016) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases. Issue 6 (1st April 2021) Authors: Poole, Olivia V.; Pizzamiglio, Chiara; Murphy, David; Falabella, Micol; Macken, William L.; Bugiardini, Enrico; Woodward, Cathy E.; Labrum, Robyn; Efthymiou, Stephanie; Salpietro, Vincenzo; Chelban, Viorica; Kaiyrzhanov, Rauan; Maroofian, Reza; Amato, Anthony A.; Gregory, Allison; Hayflick, Susan... Other Names: Alkhawaja Issam investigator.; Banu Selina investigator.; Bonsignore Maria investigator.; Breza Marianthi investigator.; Di Rosa Gabriella investigator.; Heidari Morteza investigator.; Koutsis Georgios investigator.; van den Maagdenberg Arn M.J.M. investigator.; Macaya Alfons investigator.; Münch... Journal: Annals of neurology Issue: Volume 89:Issue 6(2021) Page Start: 1240 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia. Issue 8 (1st June 2017) Authors: Chelban, Viorica; Tucci, Arianna; Lynch, David S; Polke, James M; Santos, Liana; Jonvik, Hallgeir; Groppa, Stanislav; Wood, Nicholas W; Houlden, Henry Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 88:Issue 8(2017) Page Start: 681 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗