Tuesday, June 6, 2017
- 1:45pm-3:15pm
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Cerebrospinal fluid biomarkers in Huntington’s disease – a longitudinal study
Huntington's Disease · Exhibit Hall C
- 1:45pm-3:15pm
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Cerebrotendinous xanthomatosis without tendon xanthoma: a diagnostic challenge.
Rare Genetic and Metabolic Diseases · Exhibit Hall C
- 1:45pm-3:15pm
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Changes in saccade performance with oculomotor task repetition in neurological disorders
Pathophysiology (Other Movement Disorders) · Exhibit Hall C
- 1:45pm-3:15pm
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Characteristics of tremor caused by non-olivary lesion of the medulla oblongata
Tremor · Exhibit Hall C
- 1:45pm-3:15pm
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Characterization of GNB1 mutations as a cause of global developmental delay in combination with dystonia, ataxia, or chorea in children
Genetics (Non-PD) · Exhibit Hall C
- 1:45pm-3:15pm
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Characterizing the Bcl-2 Associated Athanogene 5 Interactome
Parkinson's Disease: Pathophysiology · Exhibit Hall C
- 1:45pm-3:15pm
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Citrus extract A protects dopaminergic neuron by modulating mitochondrial respiration and reactive oxygen species
Parkinson's Disease: Pathophysiology · Exhibit Hall C
- 1:45pm-3:15pm
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Clinical and genetic analysis of ataxic patients with CACNA1A mutations in Taiwan
Genetics (Non-PD) · Exhibit Hall C
- 1:45pm-3:15pm
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Clinical and genetic characterization of Huntington’s disease in relation to the age and type of onset.
Huntington's Disease · Exhibit Hall C
- 1:45pm-3:15pm
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Clinical Experience with Initiation of Carbidopa/Levodopa Enteral Suspension in Parkinson’s Disease Patients with Cognitive Impairment
Therapy in Movement Disorders · Exhibit Hall C
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