Aya Ikeda
Tokyo, 1138421, Japan
Last Updated: 09/26/2026
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Found 20 publications
Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease.
Journal: Neurobiology of disease
Published: January 08, 2024
Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10-what distinguishes the two?
Journal: Frontiers in cell and developmental biology
Published: July 17, 2022
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson's disease.
Journal: NPJ Parkinson's disease
Published: May 06, 2022
Genetic analysis of ATP10B for Parkinson's disease in Japan.
Journal: Parkinsonism & related disorders
Published: April 05, 2021
Homeostatic p62 levels and inclusion body formation in CHCHD2 knockout mice.
Journal: Human molecular genetics
Published: September 30, 2020
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.
Journal: Neurobiology of aging
Published: March 05, 2020
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.
Journal: Journal of human genetics
Published: November 27, 2019
Mutations in CHCHD2 cause α-synuclein aggregation.
Journal: Human molecular genetics
Published: May 30, 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.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: June 14, 2018
GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.
Journal: Journal of neurology
Published: April 07, 2018
Last Updated: 09/26/2026