Monday, September 23, 2019
- 1:45pm-3:15pm
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Gene panel testing in movement disorders: an efficient approach highlighting overlaps and heterogeneity
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Generalised Polymyoclonus In a Patient With Central Nervous System Tuberculosis
Myoclonus · Les Muses, Level 3
- 1:45pm-3:15pm
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Genetic analysis of DNA methylation and hydroxymethylation genes in Parkinson’s disease
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Genetic diagnosis of Chorea-acanthocytosis using whole exome sequencing revealed novel VPS13A Gene mutation
Choreas (Non-Huntington’s Disease) · Les Muses, Level 3
- 1:45pm-3:15pm
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Genetic markers revealed in dysregulated pathways in ischemic stroke may lead to Parkinson’s disease
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Genetic panel testing in Parkinson’s disease
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Genetic polymorphism (rs6971) in translocator protein (TSPO) and its clinical relevance in Parkinson’s disease
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Genetic study of patients with Parkinson’s disease subjected to second line therapies
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
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Genetics of Parkinson’s in India – Young Onset Parkinson’s Disease (GOPI-YOPD) – A Preliminary Demographic profile
Other · Agora 2 West, Level 2
- 1:45pm-3:15pm
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Genotype-Phenotype correlations of Episodic Ataxia (EA). MDSGene Systematic Review
Ataxia · Les Muses, Level 3
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