Author

Risa Nagatomo

Institution: Kagoshima University

Observed institution: Kagoshima University

ORCID: 0009-0009-8800-2994

Observed ORCID: 0009-0009-8800-2994

OpenAlex ID: A5093306643

Genetic spectrum and clinical features of PMP22 point mutations in Japanese Charcot–Marie–Tooth disease

2026 · Chikashi Yano, Masahiro Ando, et al. · Journal of Neurology · 1

Biallelic SIGMAR1 variants in early-onset distal hereditary motor neuropathy: A Japanese case series

2026 · Kento Kodama, Masahiro Ando, et al. · Journal of Neuromuscular Diseases

Longitudinal motor function and biomarker correlates in treated adult spinal muscular atrophy: a single-center cohort study

2026 · Chikashi Yano, Masahiro Ando, et al. · Frontiers in Neurology

Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila models

2026 · Masahiro Ando, Yuji Okamoto, et al. · Neurotherapeutics

INF2 ‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights

2025 · Chikashi Yano, Masahiro Ando, et al. · Annals of Clinical and Translational Neurology

Systemic mitochondrial involvement in mitochondrial myopathy with episodic hyper-creatine kinase-emia: insights from an autopsy case

2025 · Risa Nagatomo, Yu Hiramatsu, et al. · Journal of Neurology

A case of myofibrillary myopathy due to Bcl2-Associated Athanogene 3 (BAG3) mutation complicated by peripheral neuropathy

2023 · Risa Nagatomo, Yujiro Higuchi, et al. · Rinsho Shinkeigaku

Treatment experience of introducing Nusinersen in five adults with spinal muscular atrophy type 3

2019 · Risa Nagatomo · Japanese Society of Neurology

Works count: 8

Citation count: 1

H-index: 1

I10-index: