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Genome-wide association studies of motor and cognitive progression in Parkinson’s disease
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Genome-wide association study identifies common genetic variants associated with cervical dystonia
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Genotype-phenotype correlations in 104 Uzbekish families with Spinocerebellar ataxias
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Ginsenoside Rb1 protects dopaminergic neurons through Foxm1-Nurr1 pathway in mice model of Parkinson’s disease
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Global Improvement and Patient Satisfaction: Results from a Long-Term, Open-Label, Rollover Study of Valbenazine in Tardive Dyskinesia
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Globus pallidus deep brain stimulation (GPi-DBS) in one patient with complex early-onset dystonia and KMT2B mutation: A case report
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Gluten sensitivity in progressive cerebellar ataxia patients from India
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Good response to bilateral GPI-DBS after 2 years in generalized dystonia due to a mutation in the KMT2B gene (DYT28)
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Gradient-like representation of emotional valence and arousal within the subthalamic nucleus in Parkinson’s disease
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Gut microbiota geography in Parkinson’s disease in the world
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