Shinsui Tatsumi
Nagakute, Japan
Last Updated: 09/26/2026
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Found 19 publications
An Autopsy Confirmed Neuromyelitis Optica Spectrum Disorder with Extensive Brain White Matter Lesion and Optic Neuritis but Intact Spinal Cord, Clinically Mimicking a Secondary Progressive Multiple Sclerosis-like Course.
Journal: Internal medicine (Tokyo, Japan)
Published: October 14, 2021
A Case of Anti-CRMP5 Paraneoplastic Neurological Syndrome Induced by Atezolizumab for Small Cell Lung Cancer.
Journal: Internal medicine (Tokyo, Japan)
Published: August 14, 2020
Amyotrophic Lateral Sclerosis after Receiving the Human Papilloma Virus Vaccine: A Case Report of a 15-year-old Girl.
Journal: Internal medicine (Tokyo, Japan)
Published: February 13, 2018
An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbances.
Journal: Neuropathology : official journal of the Japanese Society of Neuropathology
Published: July 15, 2015
Decreased regional cerebral blood flow in the bilateral thalami and medulla oblongata determined by an easy Z-score (eZIS) analysis of (99m)Tc-ECD-SPECT images in a case of MM2-thalamic-type sporadic Creutzfeldt-Jakob disease.
Journal: Journal of the neurological sciences
Published: April 10, 2015
Ultrastructural differences in pretangles between Alzheimer disease and corticobasal degeneration revealed by comparative light and electron microscopy.
Journal: Acta neuropathologica communications
Published: November 05, 2014
Gerstmann-Straeussler-Scheinker disease with P102L prion protein gene mutation presenting with rapidly progressive clinical course.
Journal: Clinical neuropathology
Published: July 03, 2014
Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology.
Journal: Journal of the neurological sciences
Published: January 18, 2014
Lower motor neuron involvement in TAR DNA-binding protein of 43 kDa-related frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Journal: JAMA neurology
Published: January 01, 2014
Argyrophilic grains are reliable disease-specific features of corticobasal degeneration.
Journal: Journal of neuropathology and experimental neurology
Published: December 17, 2013
Senile onset frontotemporal lobar degeneration with TAR-DNA binding protein 43 proteinopathy primarily presenting with wasteful habits.
Journal: Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society
Published: December 03, 2013
Last Updated: 09/26/2026