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Normative Curves for Selected Unified Huntington Disease Rating Scale Measures
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Normative Reference for Timed Up and Go Test (TUG) in Young Indian Adults- Preliminary Results
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Novel compound heterozygous mutations in the TSFM gene causes childhood-onset chorea
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Novel exploratory outcome assessments in GENERATION HD1
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Novel familial HPCA mutation associated with autosomal recessive dystonia: Strengthening the role of HPCA in hereditary movement disorders.
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Novel Mutation of NUS1 Gene Presenting With Developmental And Epileptic Encephalopathy and Movement Disorders
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Novel p.Pro193Arg missense mutation in ABCD1-gene associated with phenotype of ALD/AMN: a case report
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Nrf2 pathway in patients with Parkinson’s disease
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NS-PARK cohort: a nationwide real life longitudinal cohort of PD patients
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Number of people with Parkinson’s dementia in New Zealand
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