Akira Inukai

Memorial Hospital of South Bend — United States

Neuroscience · Life Sciences

17h-index1.7kcitations51works1.32yr avg
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Research Topics

Genetic Neurodegenerative Diseases(13), Muscle Physiology and Disorders(10), Neurogenetic and Muscular Disorders Research(7), Parkinson's Disease Mechanisms and Treatments(6), Mitochondrial Function and Pathology(5)

Publications49 total

A family with nonsynonymous mutations of filamin C actin-binding domain
Rinsho Shinkeigaku·2025Open Access
Patient with Heterotopic Ossification Post-SARS‑CoV‑2 Infection Regained Ability to Walk Independently Indoors after Rehabilitation and Drug Therapy：A Case Report
The Japanese Journal of Rehabilitation Medicine·2024Open Access
Analysis of medication and prescription background risk factors contributing to oral medication administration errors by nurses: A case–control study
Medicine·2022Open Access
Combined Use of 123i-fp-cit Spect and 123i-mibg Scintigraphy for Differentiation of Progressive Supranuclear Palsy Subtypes and Parkinson's Disease
2020Open Access
A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies
Journal of the Neurological Sciences·2019· 3 cited
Longitudinal Change of DAT SPECT in Parkinson’s Disease and Multiple System Atrophy
Journal of Parkinson s Disease·2019· 24 cited
Quality of life and associated factors in patients with Parkinson's disease
Japanese Journal of Health and Human Ecology·2019Open Access
An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy
Prion·2018· 4 citedOpen Access
PD-1 inhibitor-related pneumonitis in patients with minimal interstitial lung shadows before treatment
Annals of Oncology·2018Open Access
Elevated catecholamine levels in sporadic Creutzfeldt-Jakob disease
Journal of the Neurological Sciences·2017
Efficacy and safety of morphine in amyotrophic lateral sclerosis
Journal of the Neurological Sciences·2017
The effect of tracheostomy on survival in amyotrophic lateral sclerosis with severe bulbar symptoms
Journal of the Neurological Sciences·2017
A useful marker (change of MDS-UPDRS part 2 score) of underlying pathophysiological progression assessed with [123I]FP-CIT SPECT in patients with Parkinson’s disease
Journal of the Neurological Sciences·2017
Clinical and imaging findings of progressive supranuclear palsy with predominant cerebellar ataxia
Movement Disorders·2016· 14 cited
The characteristics of camptocormia in patients with Parkinson's disease: A large cross-sectional multicenter study in Japan
Journal of the Neurological Sciences·2015· 14 cited
Spinocerebellar ataxia type 31（SCA31）の臨床像，画像所見―Spinocerebellar ataxia type 6（SCA6）との小脳外症候の比較検討―
2014
A case of rapidly progressive syringomyelia due to a spinal hemangioblastoma
Rinsho Shinkeigaku·2014· 3 citedOpen Access
Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)
Rinsho Shinkeigaku·2014· 10 citedOpen Access
Camptocormia in Parkinson's disease: A multicenter study in Japan
Journal of the Neurological Sciences·2013
Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurology·2011· 211 cited
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Frequent Co-authors

Gen Sobue(22), Manabu Doyu(12), Ikuko Aiba(12), Yufuko Saito(9), Masahisa Katsuno(8), Rina Hashimoto(7), Yideng Liang(6), T. Katayama(6), Satosi Kuru(5), Yasushi Kobayashi(5), Satoko Sakakibara(5), Hiroaki Adachi(4), Mari Yoshida(4), Hirohisa Watanabe(4), Yukio Ando(4), Masahiko Yamamoto(4), Paul J. Hagerman(4), Daman Kumari(4), Karen Usdin(4), Makoto Minamiyama(3)