Michiaki Kinoshita
Azumino, 3998292, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Estimation of pathological lesion stage from brain images.
Journal: Journal of the neurological sciences
Published: November 27, 2023
An autopsy case report of a patient with frontotemporal dementia with motor neuron disease in totally locked-in state showing hyperosmolar hyperosmotic state
Journal: Rinsho shinkeigaku = Clinical neurology
Published: July 24, 2022
Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP).
Journal: eNeurologicalSci
Published: July 31, 2020
An Elderly Case of Paraneoplastic Anti-NMDA Receptor Encephalitis Associated with Small-cell Lung Cancer Expressing NR1 Subunits.
Journal: Internal medicine (Tokyo, Japan)
Published: June 05, 2020
Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: lesion staging and dynamic changes of axons and microglial subsets.
Journal: Brain pathology (Zurich, Switzerland)
Published: March 04, 2016
Expression of N-methyl-D-aspartate receptor subunits in the bovine ovum: ova as a potential source of autoantigens causing anti-NMDAR encephalitis.
Journal: The Tohoku journal of experimental medicine
Published: March 20, 2015
Corpus callosum atrophy in patients with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: an MRI-based study.
Journal: Internal medicine (Tokyo, Japan)
Published: January 07, 2014
Identification of the N-Methyl-D-aspartate receptor (NMDAR)-related epitope, NR2B, in the normal human ovary: implication for the pathogenesis of anti-NMDAR encephalitis.
Journal: The Tohoku journal of experimental medicine
Published: May 08, 2013
Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R.
Journal: Internal medicine (Tokyo, Japan)
Published: February 16, 2013
Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: case report.
Journal: Journal of the neurological sciences
Published: February 29, 2012
A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine.
Journal: Clinical neurology and neurosurgery
Published: February 28, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026