Publications by authors named "Hitoshi Arata"

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[Two cases of Perry disease (Perry syndrome) in the same family with normal I-metaiodobenzylguanidine (MIBG) myocardial scintigraphy].
Yoshito Take, Ryuji Saigo, Hitoshi Arata, Yusuke Sakiyama, Kimiyoshi Arimura

Rinsho Shinkeigaku· February 2025

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Anti-ganglionic acetylcholine receptor antibodies in functional neurological symptom disorder/conversion disorder.
Ryusei Nagata, Eiji Matsuura, Satoshi Nozuma, Mika Dozono, Yutaka Noguchi, Hitoshi Arata

Front Neurol· February 2023

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The application of shotgun metagenomics to the diagnosis of granulomatous amoebic encephalitis due to Balamuthia mandrillaris: a case report.
Shota Hirakata, Yusuke Sakiyama, Akiko Yoshimura, Mei Ikeda, Katsunori Takahata, Hitoshi Arata

BMC Neurol· October 2021

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Correlation between clinical and radiologic features of patients with Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu).
Michiyoshi Yoshimura, Jun-Hui Yuan, Keiko Higashi, Akiko Yoshimura, Hitoshi Arata

J Neurol Sci· August 2018

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Toxocara canis myelitis involving the lumbosacral region: a case report.
Yu Hiramatsu, Michiyoshi Yoshimura, Ryuji Saigo, Hitoshi Arata, Yuji Okamoto

J Spinal Cord Med· March 2017

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New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan.
Yusuke Sakiyama, Naoaki Kanda, Yujiro Higuchi, Michiyoshi Yoshimura, Hiroyuki Wakaguri, Hitoshi Arata

Neurol Neuroimmunol Neuroinflamm· October 2015

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Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs.
Akihiro Hashiguchi, Yujiro Higuchi, Miwa Nomura, Tomonori Nakamura, Hitoshi Arata

J Peripher Nerv Syst· December 2014

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[Neurological common diseases in the super-elder society. Topics: V. Dizziness, faintness, numbness and insomnia; 2. Important point of the diagnosis of numbness in hands and feet in elderly people].
Michiyoshi Yoshimura, Hitoshi Arata, Takahisa Deguchi, Hiroshi Takashima

Nihon Naika Gakkai Zasshi· August 2014

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[New era of laboratory testing. Topics: II. Particulars; 10. Novel development of biomarker in nervous disease].
Hitoshi Arata, Ryuichi Okubo, Osamu Watanabe, Hiroshi Takashima, Teruto Hashiguchi

Nihon Naika Gakkai Zasshi· December 2013

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[Anti-aquaporin-4 antibody autoimmune syndrome with disturbance of consciousness, respiratory failure, and ophthalmoplegia associated with extensive brain stem involvement with intractable hiccup and nausea as an initial manifestation. A case report].
Toru Kai, Seiichiro Tajima, Hitoshi Arata, Shigeaki Hayashi, Tatsui Nagado

Rinsho Shinkeigaku· April 2011

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[Familial prion disease (GSS, familial CJD, FFI)].
Hitoshi Arata, Hiroshi Takashima

Nihon Rinsho· August 2007

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Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
Ryuki Hirano, Hiroshi Takashima, Ryuichi Okubo, Keiko Tajima, Yuji Okamoto, Hitoshi Arata

Neurogenetics· December 2004

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Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
Takayo Arisato, Ryuichi Okubo, Hitoshi Arata, Koji Abe, Kei Fukada

Acta Neuropathol· December 2003

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