Osamu Onodera
www.mendeley.com
0000-0003-3354-5472
Niigata University
6 papers found
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Cerebellar compensation: a case of aphasia due to cerebellar hemorrhage
Marked laterality of olivopontocerebellar pathology in an autopsied patient with MSA: Implications for degeneration and α-synuclein propagation
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation
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