Publications by authors named "Takehiro Ueda"

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[A case of Candida meningitis in a patient with CARD9 deficiency: an autopsy report].
Takashi Katakami, Takehiro Ueda, Manabu Nagata, Kimiko Inoue, Yasuhumi Kageyama

Rinsho Shinkeigaku· September 2024

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Efficacy and safety of mycophenolate mofetil for steroid reduction in neuromyelitis optica spectrum disorder: a prospective cohort study.
Ritsu Akatani, Norio Chihara, Shusuke Koto, Sotaro Mori, Takuji Kurimoto, Takehiro Ueda

Immunol Med· June 2024

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Significant efficacy of electroconvulsive therapy on the behavioural symptoms of anti-N-methyl-d-aspartate receptor encephalitis.
Saehyeon Kim, Kohei Horiuchi, Takehiro Ueda, Shuken Boku

BMJ Case Rep· February 2024

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[Cingulate seizure as a clinical manifestation of anti-myelin oligodendrocyte glycoprotein antibody-positive cerebral cortical encephalitis of two cases].
Tomoko Tanaka, Masaya Togo, Kiminobu Okayama, Norio Chihara, Takehiro Ueda

Rinsho Shinkeigaku· July 2023

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A case of Cockayne syndrome with unusually mild clinical manifestations.
Mariko Tsujimoto, Eiji Nakano, Yuka Nakazawa, Fumio Kanda, Takehiro Ueda

J Dermatol· April 2023

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Clinical trial on the efficacy and safety of NPC-15 for patients with xeroderma pigmentosum exaggerated sunburn reaction type: XP-1 study protocol for a multicentre, double-blinded, placebo-controlled, two-group crossover study followed by a long-term open study in Japan.
Mariko Tsujimoto, Yasumasa Kakei, Nozomi Yamano, Takeshi Fujita, Takehiro Ueda

BMJ Open· March 2023

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Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous Variant.
Kento Matoba, Norio Chihara, Wataru Satake, Hideki Tokuoka, Yoshihisa Otsuka, Takehiro Ueda

Neurol Genet· October 2022

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Clinical and pathological characteristics of later onset multiple system atrophy.
Hiroaki Sekiya, Shunsuke Koga, Yoshihisa Otsuka, Norio Chihara, Takehiro Ueda

J Neurol· August 2022

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Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease.
Masahiro Ando, Yujiro Higuchi, Junhui Yuan, Akiko Yoshimura, Takaki Taniguchi, Takehiro Ueda

Ann Clin Transl Neurol· July 2022

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Immunotherapy-responsive Non-paraneoplastic Encephalitis with Antibodies against GAD, LGI1, and GABA Receptor.
Takahiro Nakano, Norio Chihara, Kento Matoba, Hisatsugu Tachibana, Shiho Okuda, Takehiro Ueda

Intern Med· February 2022

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[A case of spinal cord infarction accompanied with neuromyelitis optica spectrum pathophysiology].
Kimitaka Katanazaka, Norio Chihara, Sayaka Akazawa, Takehiro Ueda, Kenji Sekiguchi

Rinsho Shinkeigaku· February 2021

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[Successful treatment of Guillain-Barré syndrome-like acute inflammatory demyelinating polyneuropathy caused by pembrolizumab with a combination of corticosteroid and immunoglobulins: a case report].
Rei Hashimoto, Takehiro Ueda, Yukio Tsuji, Yoshihisa Otsuka, Kenji Sekiguchi

Rinsho Shinkeigaku· November 2020

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Progressive length-dependent polyneuropathy in xeroderma pigmentosum group A.
Yukio Tsuji, Takehiro Ueda, Kenji Sekiguchi, Masahiro Nishiyama, Fumio Kanda

Muscle Nerve· October 2020

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Diaphragm involvement in immune checkpoint inhibitor-related myositis.
Kenji Sekiguchi, Rei Hashimoto, Yoshikatsu Noda, Hisatsugu Tachibana, Yoshihisa Otsuka, Takehiro Ueda

Muscle Nerve· October 2019

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[Increased disease activity in a case of multiple sclerosis after switching treatment from fingolimod to natalizumab].
Ritsu Akatani, Norio Chihara, Kimitaka Katanazaka, Takehiro Ueda, Kenji Sekiguchi

Rinsho Shinkeigaku· August 2019

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Novel pathogenic gene mutations in Japanese patients with chorea-acanthocytosis.
Yoshiaki Nishida, Masayuki Nakamura, Yuka Urata, Kei Kasamo, Hanae Hiwatashi, Takehiro Ueda

Neurol Genet· June 2019

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Characteristics of Xeroderma Pigmentosum in Japan: Lessons From Two Clinical Surveys and Measures for Patient Care.
Chikako Nishigori, Eiji Nakano, Taro Masaki, Ryusuke Ono, Seiji Takeuchi, Takehiro Ueda

Photochem Photobiol· January 2019

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Paraneoplastic NMOSD associated with EG junction adenocarcinoma expressing unprotected AQP4.
Atsushi Sudo, Norio Chihara, Yu Takenaka, Tetsu Nakamura, Takehiro Ueda

Neurol Neuroimmunol Neuroinflamm· September 2018

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Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
Yujiro Higuchi, Ryuta Okunushi, Taichi Hara, Akihiro Hashiguchi, Junhui Yuan, Takehiro Ueda

Brain· June 2018

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Low signal intensity in motor cortex on susceptibility-weighted MR imaging is correlated with clinical signs of amyotrophic lateral sclerosis: a pilot study.
Hironobu Endo, Kenji Sekiguchi, Hitoshi Shimada, Takehiro Ueda, Hisatomo Kowa

J Neurol· March 2018

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[Retinal vasculopathy with cerebral leukoencephalopathy carrying TREX1 mutation diagnosed by the intracranial calcification: a case report].
Ryouhei Komaki, Takehiro Ueda, Yukio Tsuji, Toko Miyawaki, Sentaro Kusuhara

Rinsho Shinkeigaku· February 2018

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Quantitative analysis of brain atrophy in patients with xeroderma pigmentosum group A carrying the founder mutation in Japan.
Takehiro Ueda, Fumio Kanda, Masahiro Nishiyama, Chikako Nishigori, Tatsushi Toda

J Neurol Sci· October 2017

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Japanese de novo mutation diagnosed by exome analysis: A case report.
Hironobu Endo, Takeshi Uenaka, Wataru Satake, Yutaka Suzuki, Hisatsugu Tachibana, Takehiro Ueda

Neurol Clin Neurosci· July 2017

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Regional glucose hypometabolic spread within the primary motor cortex is associated with amyotrophic lateral sclerosis disease progression: A fluoro-deoxyglucose positron emission tomography study.
Hironobu Endo, Kenji Sekiguchi, Takehiro Ueda, Hisatomo Kowa, Fumio Kanda

eNeurologicalSci· March 2017

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A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14.
Takehiro Ueda, Tsuneyoshi Seki, Kimitaka Katanazaka, Kenji Sekiguchi, Kazuhiro Kobayashi

J Neurol· June 2013

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