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Differences in the presentation and progression of Parkinson's disease by sex
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts
De novo SPAST mutations may cause a complex SPG4 phenotype
"Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
Reliability and Validity of the Range of Motion Scale (ROMS) in Patients with Abnormal Postures
Normal eyeblink classical conditioning in patients with fixed dystonia
Early Onset Dystonia and Parkinsonism With Abnormal Globus Pallidal Signal in MRI: A Diagnostic Challenge
Is TOR1A a risk factor in adult-onset primary torsion dystonia?
Mutational analysis of TARDBP in Parkinson's disease
Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in TPP1, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease)
Cervical dystonia and genetic common variation in the dopamine pathway
Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
DYT6 Dystonia: Mutation Screening, Phenotype, and Response to Deep Brain Stimulation