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Genetics of Parkinson’s in India – Young Onset Parkinson’s Disease (GOPI-YOPD) – A Preliminary Demographic profile
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Genomic variants associated with cognitive impairment in Parkinson’s disease: Ethnicity-specific GWAS
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Genotype influences circuit compensation in Parkinson’s disease
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Genotype-Phenotype correlations of Episodic Ataxia (EA). MDSGene Systematic Review
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Genotype-phenotype relations for the isolated Dystonia Genes TOR1A, THAP1, GNAL, ANO3, KMT2B, PRKRA and HPCA: MDSGene Systematic Review
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Geste antagoniste in Catalan art – Santiago Rusiñol’s Laughing Girl
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Ginsenoside Rb1 Prevents MPTP-Induced Changes in Hippocampal Memory via Regulation of the α-Synuclein/PSD-95 Pathway
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Glabellar tap predicts dopamine transporter deficiency in parkinsonism
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Global implementation of efficacious voice treatment for Parkinson’s disease: LSVT LOUD in Germany, France and Japan
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GluRδ2 protein reduction in cerebellar Purkinje cells contributes to the pathogenesis of essential tremor
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