Takehiro Ueda
Kobe University
30 Papers
30 Citations
Takehiro Ueda is an academic researcher from Kobe University. The author has contributed to research in topics: Medicine & Xeroderma pigmentosum. The author has an hindex of 6, co-authored 20 publications.
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Papers
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
Yujiro Higuchi,Ryuta Okunushi,Taichi Hara,Akihiro Hashiguchi,Junhui Yuan,Akiko Yoshimura,Kei Murayama,Akira Ohtake,Masahiro Ando,Yu Hiramatsu,Satoshi Ishihara,Satoshi Ishihara,Hajime Tanabe,Yuji Okamoto,Eiji Matsuura,Takehiro Ueda,Tatsushi Toda,Tatsushi Toda,Sumimasa Yamashita,Kenichiro Yamada,Takashi Koide,Hiroaki Yaguchi,Jun Mitsui,Hiroyuki Ishiura,Jun Yoshimura,Koichiro Doi,Shinichi Morishita,Ken Sato,Masanori Nakagawa,Masamitsu Yamaguchi,Shoji Tsuji,Hiroshi Takashima +31 more
TL;DR: Rec recessive mutations in the mitochondrial gene, cytochrome c oxidase assembly factor 7 (COA7) in four unrelated patients with an axonal-type motor and sensory neuropathy with ataxia are identified.
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Neuroimaging features of xeroderma pigmentosum group A.
TL;DR: Brain atrophy in conventional sequences, decreased fractional anisotropy value in DTI, and reduced NAA/Cre ratio in MRS were observed in the adult patients, andMultimodal MRI studies unmask the neurological deterioration in XPA patients.
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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,Mariko Tsujimoto,Takehiro Ueda +6 more
TL;DR: The frequency of skin cancers in patients with XP has decreased in these 20 years, and the age of onset of developing skin cancers is higher than those previously observed, owing to early diagnosis and education to patients and care takers on strict prevention from sunlight.
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"Dropped head syndrome" caused by Lambert-Eaton myasthenic syndrome.
TL;DR: A 67‐year‐old man was admitted with a 2‐year history of dropped head, and serum anti‐P/Q‐voltage‐gated calcium channel antibody was positive, confirming the diagnosis of Lambert–Eaton myasthenic syndrome (LEMS).
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Paraneoplastic NMOSD associated with EG junction adenocarcinoma expressing unprotected AQP4.
Atsushi Sudo,Norio Chihara,Yu Takenaka,Tetsu Nakamura,Takehiro Ueda,Kenji Sekiguchi,Tatsushi Toda +6 more
TL;DR: A paraneoplastic NMOSD case with adenocarcinoma of the esophagogastric (EG) junction that exhibited immunoreactivity to AQP4 and negative for PD-L1 expression is reported.
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