Hirokazu Furuya
Overview
Explore the profile of Hirokazu Furuya including associated specialties, affiliations and a list of published articles.
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90
Citations
1304
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Recent Articles
1.
Furuya H
Brain Nerve
. 2023 Dec;
75(12):1325-1329.
PMID: 38097222
The Labours of Hercules, written by Agatha Christie, contains twelve short stories, with 'atropine' playing a crucial role in the seventh story, The Cretan Bull (1939). Atropine easily crosses the...
2.
Shogase T, Ohtsuru S, Morita Y, Osaki Y, Furuya H, Anayama T
Rinsho Shinkeigaku
. 2023 Feb;
63(2):92-96.
PMID: 36725010
A 74-year-old Japanese woman, who had been previously diagnosed as ocular myasthenia gravis (MG), presented to our hospital complaining of dropped head and increased fatiguability while eating. The edrophonium test...
3.
Chadani Y, Kashibayashi T, Yamamoto T, Tsuda A, Fujito R, Akamatsu M, et al.
Sci Rep
. 2022 Nov;
12(1):20428.
PMID: 36443371
Apathy is frequently observed in idiopathic normal pressure hydrocephalus (iNPH) and worsens cognitive impairment and gait disturbance. In this study, we evaluated the regions associated with apathy in iNPH using...
4.
Oki R, Izumi Y, Fujita K, Miyamoto R, Nodera H, Sato Y, et al.
JAMA Neurol
. 2022 May;
79(6):575-583.
PMID: 35532908
Importance: The effectiveness of currently approved drugs for amyotrophic lateral sclerosis (ALS) is restricted; there is a need to develop further treatments. Initial studies have shown ultrahigh-dose methylcobalamin to be...
5.
Miyagawa T, Tanaka S, Shimada M, Sakai N, Tanida K, Kotorii N, et al.
NPJ Genom Med
. 2022 Apr;
7(1):29.
PMID: 35414074
Idiopathic hypersomnia (IH) is a rare, heterogeneous sleep disorder characterized by excessive daytime sleepiness. In contrast to narcolepsy type 1, which is a well-defined type of central disorders of hypersomnolence,...
6.
Umemoto G, Fujioka S, Arahata H, Sakae N, Sasagasako N, Toda M, et al.
BMC Neurol
. 2021 Aug;
21(1):302.
PMID: 34353291
Background: Swallowing dysfunction is related to major cause of adverse events and an indicator of shorter survival among patients with neuromuscular disorders (NMD). It is critical to assess the swallowing...
7.
Mori S, Honda H, Hamasaki H, Sasagasako N, Suzuki S, Furuya H, et al.
Neuropathology
. 2021 May;
41(4):253-265.
PMID: 34031922
Spastic paraplegia type 11 (SPG11) is the most common autosomal recessive hereditary spastic paraplegia with thinning of the corpus callosum. Spatacsin, a protein encoded by the SPG11 gene, is associated...
8.
Odaka H, Numakawa T, Soga M, Kido J, Matsumoto S, Kajihara R, et al.
Neurobiol Dis
. 2021 Jan;
152:105279.
PMID: 33516873
Sialidosis is a neuropathic lysosomal storage disease caused by a deficiency in the NEU1 gene-encoding lysosomal neuraminidase and characterized by abnormal accumulation of undigested sialyl-oligoconjugates in systemic organs including brain....
9.
Mori S, Suzuki S, Honda H, Hamasaki H, Sakae N, Sasagasako N, et al.
Neuropathology
. 2021 Jan;
41(2):146-151.
PMID: 33404144
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disease, characterized by the progressive ossification of skeletal muscles, fascia, tendons, and ligaments. In most cases, the great toes of patients...
10.
Osaki Y, Morita Y, Miyamoto Y, Ohtsuru S, Shogase T, Furushima T, et al.
Acta Neurol Scand
. 2020 Oct;
143(3):313-317.
PMID: 33111976
Objectives: A pre-possible multiple system atrophy (MSA) phase, that is, the period between symptom onset and satisfying the second consensus diagnostic criteria for possible or probable MSA, may exist. The...