Tuesday, June 6, 2017
- 1:45pm-3:15pm
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Assessments of Movement Disorder Symptoms and Functional Impacts in Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)
Rare Genetic and Metabolic Diseases · Exhibit Hall C
- 1:45pm-3:15pm
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Association analysis of single nucleotide polymorphisms near the DYT3 locus to dystonic symptoms in X-linked dystonia-parkinsonism
Genetics (Non-PD) · Exhibit Hall C
- 1:45pm-3:15pm
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Association of CSF biomarkers with motor and non-motor features in moderately advanced Parkinson’s disease cohort: the BioFIND study
Parkinson's Disease: Pathophysiology · Exhibit Hall C
- 1:45pm-3:15pm
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Ataxia and increased cerebrospinal fluid phosphate associated with a mutation in the SLC20A2 gene
Genetics (Non-PD) · Exhibit Hall C
- 1:45pm-3:15pm
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Atypical and slowly progressive FTDP-17 caused by MAPT p.R406W mutations – similarities to AD and PSP.
Rare Genetic and Metabolic Diseases · Exhibit Hall C
- 1:45pm-3:15pm
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Autonomous Tracking of Body Bradykinesia during Unconstrained Activities in Parkinson’s Disease
Technology · Exhibit Hall C
- 1:45pm-3:15pm
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Axial signs in early-stage Parkinson’s disease : an influence of the genotype ?
Parkinson's Disease: Pathophysiology · Exhibit Hall C
- 1:45pm-3:15pm
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Barriers to exercise in newly diagnosed Parkinson’s disease
Therapy in Movement Disorders · Exhibit Hall C
- 1:45pm-3:15pm
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Baseline multimodal information predicts future motor impairment in premanifest Huntington’s disease
Huntington's Disease · Exhibit Hall C
- 1:45pm-3:15pm
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Behavioral Changes on the UCSD Huntington’s Disease Behavioral Questionnaire (HD-BQ) Distinguish Patients Transitioning to Manifest Huntington’s disease (HD)
Huntington's Disease · Exhibit Hall C
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