Saturday, October 6, 2018
- 1:45pm-3:15pm
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A new SPG4/SPAST mutation in an Italian family with hereditary spastic paraplegia and Alzheimer’s disease
Genetics (Non-PD) · Hall 3FG
- 1:45pm-3:15pm
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A novel homozygous splice site mutation in the KIF1C gene (SPAX2, SPG58) found in a consanguineous turkish family
Rare Genetic and Metabolic Diseases · Hall 3FG
- 1:45pm-3:15pm
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A novel mutation in VRK1 associated with distal spinal muscular atrophy
Genetics (Non-PD) · Hall 3FG
- 1:45pm-3:15pm
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A novel non-nitrocatechol COMT inhibitor ODM-104 shows superior pharmacodynamic effects to entacapone
- 1:45pm-3:15pm
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A Patient-Centered Decision-Making Algorithm for Deep Brain Stimulation Surgery in Parkinson’s Disease
Surgical Therapy: Parkinson's Disease · Hall 3FG
- 1:45pm-3:15pm
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A Phase 2A Study of Nilotinib in Patients with Advanced and Early Parkinson’s disease: Study Design
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