Mitsuaki Oki
Hirakata, Japan
Last Updated: 09/26/2026
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Found 14 publications
A case of female dystrophinopathy with presumed childhood onset, presenting with asymmetric muscle weakness and delayed diagnosis in old age
Journal: Rinsho shinkeigaku = Clinical neurology
Published: July 08, 2026
Neurogenesis defects in iPSC-derived midbrain organoids of early-onset Parkinson's disease with 22q11.2 deletion syndrome.
Journal: Frontiers in cellular neuroscience
Published: June 11, 2026
Severe Anti-CV2/CRMP5, Anti-Hu, and Anti-SOX1 Antibody-Positive Paraneoplastic Neurological Syndrome Associated With Tumor Recurrence During Atezolizumab Therapy.
Journal: Cureus
Published: December 14, 2025
Pre-Existing Peak-Dose Dyskinesia and Light Body Weight as Predictors of Ropinirole Patch Dose Modification in Parkinson Disease: A Multicenter Retrospective Study.
Journal: Clinical neuropharmacology
Published: December 02, 2025
Zonisamide modulates cholinergic markers and alleviates levodopa-induced dyskinesia in a rat model of Parkinson's disease.
Journal: Experimental neurology
Published: April 15, 2025
Lateral Medullary Infarction Presenting as Opalski Syndrome Associated with Headache Attributed to Orthostatic Hypotension.
Journal: Internal medicine (Tokyo, Japan)
Published: April 13, 2025
Zonisamide attenuates the severity of levodopa-induced dyskinesia via modulation of the striatal serotonergic system in a rat model of Parkinson's disease.
Journal: Neuropharmacology
Published: May 13, 2021
GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.
Journal: Journal of neurology
Published: April 07, 2018
Zonisamide ameliorates levodopa-induced dyskinesia and reduces expression of striatal genes in Parkinson model rats.
Journal: Neuroscience research
Published: February 01, 2017
Weight loss in the early stage of progressive supranuclear palsy.
Journal: Brain and behavior
Published: May 28, 2016
The role of p62/SQSTM1 in sporadic inclusion body myositis.
Journal: Neuromuscular disorders : NMD
Published: April 28, 2016
Early-onset Parkinson's Disease Associated with Chromosome 22q11.2 Deletion Syndrome.
Journal: Internal medicine (Tokyo, Japan)
Published: February 03, 2016
Last Updated: 09/26/2026