Tuesday, June 21, 2016
- 12:30pm-2:00pm
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Myoclonus complicating chickenpox: A case report
Myoclonus · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Myoclonus Dystonia: A report of two rare mutations
Genetics (NON-PD) · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Neurodegeneration and microgliosis are independent of α-synuclein aggregation in a mouse model of "prion-like" α-synuclein speading
Parkinson's disease: Pathophysiology · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Neurodegeneration with brain iron accumulation (NBIA): Two cases with different subtypes and a rare mutation
Rare genetic and metabolic diseases · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Neurodegenerative disorders with atypical course and cause, diagnostic contribution of genetics and magnetic resonance imaging, two case reports
Tremor · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Neuromelanin imaging is useful for monitoring disease progression in Parkinson’s disease and PARK2
Parkinson's disease: Pathophysiology · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Neurophysiological investigation of brainstem in idiopathic REM sleep behavior disorder (iRBD) through vestibular evoked myogenic potentials (VEMPs)
Restless legs syndrome and other sleep disorders · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Next-generation profiling to identify the molecular etiology of Parkinson’s disease dementia
Parkinson's disease: Genetics · Exhibit Hall located in Hall B, Level 2
- 12:30pm-2:00pm
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Ninjurin 1 gene D110a single nucleotide polymorphism as a genetic marker for nerve damage leprosy patients from South India
Genetics (NON-PD) · Exhibit Hall located in Hall B, Level 2
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