Arisa Hayashida

Tokyo, Japan

Last Updated: 09/26/2026

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Found 19 publications

Stress-induced nuclear GAPDH: Scientific update and clinical application.

Stress-induced nuclear GAPDH: Scientific update and clinical application.

Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

Published: June 06, 2025

Correction: Nuclear GAPDH in cortical microglia mediates cellular stress-induced cognitive inflexibility.

Correction: Nuclear GAPDH in cortical microglia mediates cellular stress-induced cognitive inflexibility.

Journal: Molecular psychiatry

Published: July 02, 2024

Nuclear GAPDH in cortical microglia mediates cellular stress-induced cognitive inflexibility.

Nuclear GAPDH in cortical microglia mediates cellular stress-induced cognitive inflexibility.

Journal: Molecular psychiatry

Published: September 16, 2022

Genotype-phenotype correlation of Parkinson's disease with PRKN variants.

Genotype-phenotype correlation of Parkinson's disease with PRKN variants.

Journal: Neurobiology of aging

Published: April 30, 2021

A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels.

A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels.

Journal: International journal of molecular sciences

Published: March 10, 2021

Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.

Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.

Journal: Clinical genetics

Published: August 08, 2020

Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease.

Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease.

Journal: Frontiers in neurology

Published: June 26, 2020

The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.

The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.

Journal: Neurobiology of aging

Published: March 05, 2020

Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.

Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.

Journal: Journal of human genetics

Published: November 27, 2019

Somnolence Preceded the Development of a Subthalamic Lesion in Neuromyelitis Optica Spectrum Disorder.

Somnolence Preceded the Development of a Subthalamic Lesion in Neuromyelitis Optica Spectrum Disorder.

Journal: Internal medicine (Tokyo, Japan)

Published: October 16, 2019

Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.

Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: June 14, 2018

Myalgia caused by chronic myositis associated with plasmacytosis: a case report.

Myalgia caused by chronic myositis associated with plasmacytosis: a case report.

Journal: BMC neurology

Published: May 08, 2018

Showing 1-12 of 19

Last Updated: 09/26/2026