-
A Nomogram Model for Predicting Malnutrition among Patients with Parkinson’s Disease
-
A non-linear index can detect early postural instability in people with Parkinson’s disease: Enhancing perspectives on the utilization of cost-effective technologies.
-
A novel G413S mutation in the CSF1R gene causes Hereditary Diffuse Leucoencephalopathy with axonal Spheroids; clinically overlapping features of Parkinsonism
-
A Novel Mutation of NKX2-1 Gene: A Rare Presentation of Chorea
-
A Novel Peer Mentoring Support System for Persons with Parkinson’s Disease
-
A novel single-cell reporter identifies regulators of the endogenous PINK1-Parkin mitochondrial quality control pathway
-
A Novel SLC9A1 Mutation Associated with Cerebellar Ataxia and Sensorineural Hearing Loss
-
A pathology-validated study to investigate the role of Uric Acid in Parkinson’s Disease
-
A Patient with Overlapping SPG7 mutation and MERRF
-
A Phase 1b Randomized, Placebo-Controlled, Delayed-Start Trial of UB-312 in Synucleinopathies.
- « Previous Page
- 1
- …
- 3
- 4
- 5
- 6
- 7
- …
- 181
- Next Page »