Tuesday, June 21, 2016
- 12:30pm-2:00pm
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Same cerebellar atrophy pattern in hyper- and hypokinetic movement disorders due to mitochondrial cytopathy
Rare genetic and metabolic diseases · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Selenotranscriptomic analyses identify signature selenoproteins in brain regions in a mouse model of Parkinson’s disease
Parkinson's disease: Pathophysiology · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Sensor based gait analysis: Diagnostic application for apomorphine titration
Technology · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Serum levels of polychlorinated biphenyls, CYP2B6 and neurodegenerative disease in the Faroe Islands
Parkinson's disease: Genetics · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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sFIDA: A sensitive diagnostic assay for quantification of α-synuclein aggregates
Technology · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Sleep in essential tremor patients: A polysomnographic study
Tremor · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Sleep motor activity in amyotrophic lateral sclerosis
Restless legs syndrome and other sleep disorders · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Sleep related disorders in subtypes of patients with Parkinson’s disease in the Tomsk region, Russia
Restless legs syndrome and other sleep disorders · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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SMPD1 mutations, acid-sphingomyelinase activity and α-synuclein accumulation in Parkinson’s disease
Parkinson's disease: Genetics · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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SOD1 aggregation: A pathological link between Parkinson’s disease and amyotrophic lateral sclerosis?
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