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BMJ Case Reports|February 2, 2024
Significant efficacy of electroconvulsive therapy on the behavioural symptoms of anti-N-methyl-d-aspartate receptor encephalitisSaehyeon Kim, Kohei Horiuchi, Takehiro Ueda, et al.
Journal of the Neurological Sciences|October 10, 2017
Quantitative analysis of brain atrophy in patients with xeroderma pigmentosum group A carrying the founder mutation in JapanTakehiro Ueda, Fumio Kanda, Masahiro Nishiyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 25, 2024
[A case of Candida meningitis in a patient with CARD9 deficiency: an autopsy report]Takashi Katakami, Takehiro Ueda, Manabu Nagata, et al.
Eneurologicalsci|December 21, 2017
Regional glucose hypometabolic spread within the primary motor cortex is associated with amyotrophic lateral sclerosis disease progression: A fluoro-deoxyglucose positron emission tomography studyHironobu Endo, Kenji Sekiguchi, Takehiro Ueda, et al.
Brain and Behavior|May 11, 2012
Neuroimaging features of xeroderma pigmentosum group ATakehiro Ueda, Fumio Kanda, Nobukazu Aoyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 23, 2013
[A case of juvenile parkinsonism with expanded SCA8 CTA/CTG repeats]Toko Miyawaki, Kenji Sekiguchi, Naoko Yasui, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 26, 2019
[Increased disease activity in a case of multiple sclerosis after switching treatment from fingolimod to natalizumab]Ritsu Akatani, Norio Chihara, Kimitaka Katanazaka, et al.
Rinsho Shinkeigaku = Clinical Neurology|January 28, 2021
[A case of spinal cord infarction accompanied with neuromyelitis optica spectrum pathophysiology]Kimitaka Katanazaka, Norio Chihara, Sayaka Akazawa, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 29, 2020
[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, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 2, 2018
[Retinal vasculopathy with cerebral leukoencephalopathy carrying TREX1 mutation diagnosed by the intracranial calcification: a case report]Ryouhei Komaki, Takehiro Ueda, Yukio Tsuji, et al.
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