Yoshihisa Ikeda
Kanazawa, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
MEG activity of the dorsolateral prefrontal cortex during optic flow stimulations detects mild cognitive impairment due to Alzheimer's disease.
Journal: PloS one
Published: June 11, 2021
Chorea-acanthocytosis with a novel mutation in the vacuolar protein sorting 13 homolog a gene: A case report.
Journal: Journal of the neurological sciences
Published: December 09, 2019
Spontaneous MEG activity of the cerebral cortex during eyes closed and open discriminates Alzheimer's disease from cognitively normal older adults.
Journal: Scientific reports
Published: November 05, 2019
Higher Blood Vitamin C Levels are Associated with Reduction of Apolipoprotein E E4-related Risks of Cognitive Decline in Women: The Nakajima Study.
Journal: Journal of Alzheimer's disease : JAD
Published: May 16, 2018
Differences in Dementia Beliefs between Non-Demented Public Screeners and In-Home Screeners and Their Potential Impact on Future Dementia Screening Intention: The Nakajima Study.
Journal: Journal of Alzheimer's disease : JAD
Published: April 05, 2018
Serum anti-aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder presenting as acute eosinophilic encephalomyelitis.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: June 07, 2017
Inclusion body myositis with granuloma formation in muscle tissue.
Journal: Neuromuscular disorders : NMD
Published: April 15, 2015
Efficacy of diflunisal on autonomic dysfunction of late-onset familial amyloid polyneuropathy (TTR Val30Met) in a Japanese endemic area.
Journal: Journal of the neurological sciences
Published: May 10, 2014
Differences in the prevalence of dementia and mild cognitive impairment and cognitive functions between early and delayed responders in a community-based study of the elderly.
Journal: Journal of Alzheimer's disease : JAD
Published: August 17, 2013
A clinical phenotype of distal hereditary motor neuronopathy type II with a novel HSPB1 mutation.
Journal: Journal of the neurological sciences
Published: June 16, 2008
Showing 1-12 of 12
Last Updated: 09/26/2026