Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Kanako Takeda"'
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Akademický článek
Mutation in the STXBP1 Gene Associated with Early Onset West Syndrome: A Case Report and Literature Review
Autor: Kanako Takeda, Yusaku Miyamoto, Hisako Yamamoto, Toshiyuki Iwasaki, Noriko Sumitomo, Eri Takeshita, Atsushi Ishii, Shinichi Hirose, Naoki Shimizu
Publikováno v: Pediatric Reports, Vol 14, Iss 4, Pp 386-395 (2022)
Syntaxin-binding protein1 (STXBP1) is a member of the Sec1/Munc18-1 protein family, which comprises important regulators of the secretory and synaptic vesicle fusion machinery underlying hormonal and neuronal transmission, respectively. STXBP1 pathog
Externí odkaz: https://doaj.org/article/add70968c4fc4c6a892ca131d6bf93e4
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Extraction of Parameters for 90-degree Turn Prediction Using the IMU-based Motion Capture System
Autor: Ami Ogawa, Akira Mita, Kanako Takeda
Publikováno v: Materials Research Proceedings.
Against the increasing number of single households, we have been proposing the “Biofied Building” that provides a safe, secure, and comfortable living space for a resident using a small home robot. The robot can be used for real-time sensing of t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa1ee9f0c1455b6dab0b3181d7fb2cb2
https://doi.org/10.21741/9781644901311-29
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Structural brain network analysis of children with localization-related epilepsy
Autor: Kanako Takeda, Yusaku Miyamoto, Hiroshi Matsuda, Hitoshi Yamamoto
Publikováno v: Brain and Development. 39:678-686
Introduction Epilepsy is considered to arise from dysfunction in neural networks. Recent advances in neuroimaging and its analysis have made it possible to investigate both functional and structural connectivity in the brain. The aim of this study wa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5acef56442a9875d237d845bffaeeb2b
https://doi.org/10.1016/j.braindev.2017.04.010
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Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutation
Autor: Atsushi Ishii, Hitoshi Yamamoto, Yusaku Miyamoto, Kanako Takeda, Shinichi Hirose, Hisako Yamamoto
Publikováno v: Braindevelopment. 42(1)
Background CDKL5 deficiency is caused by mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene and clinically manifests often in females as drug-resistant intractable epilepsy and severe psychomotor retardation. Case report We report the case
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba99b0078450fe65276fab87c5aae985
https://pubmed.ncbi.nlm.nih.gov/31492455
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Proposal for a New Noncontact Method for Measuring Tongue Moisture to Assist in Tongue Diagnosis and Development of the Tongue Image Analyzing System, Which Can Separately Record the Gloss Components of the Tongue
Autor: Kanako Takeda, Koichi Nagamine, Keigo Ueda, Yoichi Miyake, Satoshi Yamamoto, Takeshi Oji, Takao Namiki, Yuya Ishikawa, Norimichi Tsumura, Toshiya Nakaguchi
Publikováno v: BioMed Research International, Vol 2015 (2015)
BioMed Research International
Tongue diagnosis is a noninvasive diagnosis and is traditionally one of the most important tools for physicians who practice Kampo (traditional Japanese) medicine. However, it is a subjective process, and its results can depend on the experience of t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d732dcfcef90fa60eb3a01343b35050
https://doaj.org/article/0b46c66b4da34480ac2f168d23620dae
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