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Movement Disorders : Official Journal of the Movement Disorder Society|August 21, 2012
THAP1 mutations and dystonia phenotypes: genotype phenotype correlationsGeorgia Xiromerisiou, Henry Houlden, Nikolaos Scarmeas, et al.Journal of Neurology|April 12, 2011
Cost-of-illness in multiple system atrophy and progressive supranuclear palsyYaroslav Winter, Maria Stamelou, Nicole Cabanel, et al.Parkinsonism & Related Disorders|July 3, 2020
DaTSCAN (123I-FP-CIT SPECT) imaging in early versus mid and late onset Parkinson's disease: Longitudinal data from the PPMI studyChristos Koros, Athina-Maria Simitsi, Andreas Prentakis, et al.Nature Reviews. Disease Primers|August 10, 2023
Frontotemporal lobar degenerationMurray Grossman, William W Seeley, Adam L Boxer, et al.Frontiers in Neuroscience|November 21, 2024
Reward processing deficits arise early in familial frontotemporal dementiaNoah G Cryns, Emily G Hardy, Ashlin R K Roy, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2018
Mediterranean diet adherence is related to reduced probability of prodromal Parkinson's diseaseMaria I Maraki, Mary Yannakoulia, Maria Stamelou, et al.Neuro-Degenerative Diseases|May 18, 2011
Health-related quality of life in multiple system atrophy and progressive supranuclear palsyYaroslav Winter, Annika E Spottke, Maria Stamelou, et al.Parkinsonism & Related Disorders|April 18, 2021
Late life psychotic features in prodromal Parkinson's diseaseIoanna Pachi, Maria I Maraki, Nikolaos Giagkou, et al.Parkinsonism & Related Disorders|May 14, 2016
Predicting disease progression in progressive supranuclear palsy in multicenter clinical trialsJee Bang, Iryna V Lobach, Anthony E Lang, et al.Brain : a Journal of Neurology|May 3, 2018
Retraining speech production and fluency in non-fluent/agrammatic primary progressive aphasiaMaya L Henry, H Isabel Hubbard, Stephanie M Grasso, et al.Pageof 43