Hidehiro Mizusawa
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Explore the profile of Hidehiro Mizusawa including associated specialties, affiliations and a list of published articles.
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354
Citations
5420
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Recent Articles
1.
Hatano Y, Ishihara T, Hirokawa S, Date H, Takahashi Y, Mizusawa H, et al.
Neurol Genet
. 2025 Feb;
11(2):e200245.
PMID: 39996131
Background And Objectives: Spinocerebellar ataxia type 6 (SCA6) is caused by expansion of CAG repeat units (RUs) in . While the pathologic threshold has been considered to be 20 or...
2.
Ohira M, Takano A, Yoshi K, Arai A, Aso Y, Furutani R, et al.
Eur J Neurol
. 2025 Jan;
32(1):e70005.
PMID: 39807698
Background And Purpose: Clinical manifestations of Lyme borreliosis (LB), caused by Borrelia burgdorferi sensu lato (Bbsl), include erythema migrans, Lyme neuroborreliosis (LNB), carditis, and arthritis. LB is a notifiable disease...
3.
Nonaka T, Ae R, Kosami K, Tange H, Kaneko M, Nakagaki T, et al.
Diagnostics (Basel)
. 2024 Nov;
14(21).
PMID: 39518392
Background/objectives: Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal neurodegenerative disorder traditionally diagnosed based on the World Health Organization (WHO) criteria in 1998. Recently, Hermann et al. proposed updated diagnostic criteria...
4.
Saitoh Y, Mizusawa H
J Neurol Sci
. 2024 Jul;
463:123119.
PMID: 39029285
Prion diseases are caused by prions, which are proteinaceous infectious particles that have been identified as causative factors of transmissible spongiform encephalopathies such as Creutzfeldt-Jakob disease (CJD). Prion diseases are...
5.
Goto R, Oba K, Bando K, Todoroki K, Yoshida J, Nishida D, et al.
Neurosci Res
. 2024 Jul;
208:39-43.
PMID: 38986955
We estimated the severity of cerebellar ataxia by analyzing gait rhythm. We measured the step times in patients with pure cerebellar ataxia and healthy controls and then analyzed the distribution...
6.
Wang D, Honda S, Shin M, Watase K, Mizusawa H, Ishikawa K, et al.
Biochem Biophys Res Commun
. 2024 Jan;
695:149481.
PMID: 38211534
Spinocerebellar ataxia type 6 (SCA6) is a polyglutamine (polyQ) disease, which is caused by the elongation of CAG repeats encoding polyQ in the CACNA1A gene. The CACNA1A gene encodes two...
7.
Matsushita M, Nakamura Y, Hosokawa T, Takahashi Y, Mizusawa H, Arawaka S
Rinsho Shinkeigaku
. 2023 Dec;
64(1):28-32.
PMID: 38072442
A 36-year-old man has developed weakness of left thumb and atrophy of left thenar muscle and left first dorsal interosseous muscle without sensory disturbance for a year. A nerve conduction...
8.
Ito M, Sugiyama A, Higuchi Y, Takashima H, Takahashi Y, Mizusawa H, et al.
Intern Med
. 2023 Dec;
63(15):2183-2186.
PMID: 38072404
Spinocerebellar ataxia type 14 (SCA14) is a rare form of autosomal dominant cerebellar ataxia caused by mutations in PRKCG. We herein report a case of SCA14 presenting with writer's cramp...
9.
Ohira M, Yoshii K, Aso Y, Nakajima H, Yamashita T, Takahashi-Iwata I, et al.
Emerg Microbes Infect
. 2023 Oct;
12(2):2278898.
PMID: 37906509
Tick-borne encephalitis (TBE) is an infection of the central nervous system caused by the tick-borne encephalitis virus (TBEV). TBE is endemic in parts of Europe and Asia. TBEV is transmitted...
10.
Fujino Y, Ueyama M, Ishiguro T, Ozawa D, Ito H, Sugiki T, et al.
Elife
. 2023 Jul;
12.
PMID: 37461319
Abnormal expansions of GGGGCC repeat sequence in the noncoding region of the gene is the most common cause of familial amyotrophic lateral sclerosis and frontotemporal dementia (C9-ALS/FTD). The expanded repeat...