Saturday, October 6, 2018
- 1:45pm-3:15pm
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Exosomal alpha synuclein secretion is beneficial for cellular models of Kufor-Rakeb syndrome
Rare Genetic and Metabolic Diseases · Hall 3FG
- 1:45pm-3:15pm
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Expanding the clinical phenotype of autosomal recessive spinocerebellar ataxia with Adult onset; a collection of case series
Genetics (Non-PD) · Hall 3FG
- 1:45pm-3:15pm
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Expanding the clinical phenotype of BPAN: A case report
Rare Genetic and Metabolic Diseases · Hall 3FG
- 1:45pm-3:15pm
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Exploring the neural correlates of gait asymmetry in idiopathic REM Sleep Behaviour Disorder
Neuroimaging (Non-PD) · Hall 3FG
- 1:45pm-3:15pm
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Explosive flurry of seizures and new-onset cortical-subcortical lesions in a patient with Wilson disease
Rare Genetic and Metabolic Diseases · Hall 3FG
- 1:45pm-3:15pm
-
Eye Movement Abnormalities Correspond to Pontine Atrophy in Wilson Disease
Pathophysiology (Other Movement Disorders) · Hall 3FG
- 1:45pm-3:15pm
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Familial SCA2-parkinsonism presented as intractable oromandibular dystonia
Genetics (Non-PD) · Hall 3FG
- 1:45pm-3:15pm
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Fasciculations from a cholinesterase inhibitor
Drug-Induced Movement Disorders · Hall 3FG
- 1:45pm-3:15pm
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Feasibility and Efficacy of Brainstem Modulation Therapy for the Management of Parkinson’s Disease
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