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Gender inequities in people living with PD and their caregivers’ burden in Mexican population
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Gender-Specific Classification Models for Parkinson’s Disease using Non-Motor Symptoms and DNA Methylation Data
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Gender-specific differences of gait in parkinsonian syndromes
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Gene rearrangement as the cause of hereditary Hypomyelinating Leukodyistrophy disease type 5 (HLD5)
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Gene-environment interactions for Parkinson’s disease
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Generalized acute myoclonus caused by chikungunya virus encephalitis: case report.
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Generalized chorea, cerebellar ataxia and spastic tetraparesis with a genetic mutation in FAT2 gene – coincidence or a new SCA45 phenotype?
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Generalized dystonia and spasticity: The fault in the mitochondria
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Genetic and functional analysis of CCDC88C mutations in patients with Parkinson’s disease.
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Genetic and phenotypic characterization of ATX-FAT2 (SCA45) in three Indian families
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