Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yoshiyuki HANAOKA"'
Autor:
Hiroshi Sakuma, Jun-ichi Takanashi, Kazuhiro Muramatsu, Hidehito Kondo, Takashi Shiihara, Motomasa Suzuki, Kazuo Okanari, Mariko Kasai, Osamu Mitani, Tomoyuki Nakazawa, Taku Omata, Konomi Shimoda, Yuichi Abe, Yoshihiro Maegaki, Kei Murayama, Yuka Murofushi, Hiroaki Nagase, Akihisa Okumura, Yasunari Sakai, Hiroko Tada, Masashi Mizuguchi, Japanese Pediatric Neuro-COVID-19 Study Group, Tsuyoshi Matsuoka, Hiroshi Oakada, Tatsuharu Sato, Kenjiro Kikuchi, Satoshi Akamine, Nanako Kawata, Shinichiro Morichi, Hideyuki Iwayama, Ryuta Tanaka, Yoshiyuki Hanaoka, Yuki Minamisawa, Tatsuya Ema, Mitsuo Motobayashi, Tomoshiro Ito, Fumikazu Sano
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Background and objectivesTo clarify whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection cause acute encephalopathy in children and which are the most common syndromes that cause them and what are the outcomes.MethodsA natio
Externí odkaz:
https://doaj.org/article/d27b86d3fea846ce99dd9d7559309e79
Autor:
Yosuke OKAZAKI, Tatsuya SASAKI, Kouji KAWAI, Kakeru HOSOMOTO, Susumu SASADA, Takao YASUHARA, Tomoyuki AKIYAMA, Yoshiyuki HANAOKA, Isao DATE
Publikováno v:
NMC Case Report Journal. 9:307-312
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5ac6891262de1694e3d278022078971
https://doi.org/10.2176/jns-nmc.2022-0084
https://doi.org/10.2176/jns-nmc.2022-0084
Autor:
Teruko Morooka, Masao Matsuhashi, Hiroki Tsuchiya, Katsuhiro Kobayashi, Makio Oka, Mari Akiyama, Yoshiyuki Hanaoka, Tomoyuki Akiyama, Takashi Shibata
Publikováno v:
Brain and Development. 43:904-911
Objective Physiological gamma and ripple activities may be linked to neurocognitive functions. This study investigated the relationship between development and non-epileptic, probably physiological, fast (40–200 Hz) oscillations (FOs) including gam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8abf0ecc30d4df2965549eef28df687
https://doi.org/10.1016/j.braindev.2021.05.004
https://doi.org/10.1016/j.braindev.2021.05.004
Autor:
Tomoyuki Akiyama, Ryousuke Miyamoto, Harumi Yoshinaga, Katsuhiro Kobayashi, Toshitaka Kawarai, Yoshiyuki Hanaoka, Ryuji Kaji
Publikováno v:
Brain and Development. 43:783-788
Background DYT-TOR1A is caused by a GAG deletion in the TOR1A gene. While it usually manifests as early-onset dystonia, its phenotype is extremely diverse, even within one family. Recent reports have revealed that some DYT-TOR1A cases have novel muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86b6ca0e0cd3abca42376785e6145eeb
https://doi.org/10.1016/j.braindev.2021.03.005
https://doi.org/10.1016/j.braindev.2021.03.005
Autor:
Naoko Maura, Mari Akiyama, Fumika Endoh, Tomoyuki Akiyama, Yoshiyuki Hanaoka, Katsuhiro Kobayashi
Publikováno v:
Journal of the Japan Epilepsy Society. 38:36-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::213280c27d0ad8657634c7b466f61b0a
https://doi.org/10.3805/jjes.38.36
https://doi.org/10.3805/jjes.38.36
Autor:
Yuki Hyodo, Tomoyuki Akiyama, Tomoshiro Ito, Soichiro Toda, Chiho Tokorodani, Yoshiyuki Hanaoka, Katsuhiro Kobayashi, Nobusuke Kimura, Hiroyuki Miyahara, Yukiko Mogami
Publikováno v:
Brain and Development. 42:402-407
Background The initial presentation of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is indistinguishable from that of complex febrile seizures (FS), which poses a great diagnostic challenge for clinicians. Excitotoxic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3581522e92ca9f4e0dcb814fc37c706c
https://doi.org/10.1016/j.braindev.2020.02.002
https://doi.org/10.1016/j.braindev.2020.02.002
Autor:
Tomoyuki Akiyama, Katsuhiro Kobayashi, Mari Akiyama, Yoshiyuki Hanaoka, Tokito Yamaguchi, Takashi Shibata, Yumiko Hayashi, Hiroki Tsuchiya
Publikováno v:
Clinica Chimica Acta. 472:118-122
We quantified pyridoxal 5'-phosphate (PLP), pyridoxal (PL), and 4-pyridoxic acid (PA) in paired serum and cerebrospinal fluid (CSF) samples from children and investigated the effect of age on the concentrations and CSF-to-serum ratios of these vitame
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a39e47b8b43745d90f9ce65bba0a10
https://doi.org/10.1016/j.cca.2017.07.032
https://doi.org/10.1016/j.cca.2017.07.032
Autor:
Takashi Agari, Harumi Yoshinaga, Mari Akiyama, Isao Date, Fumika Endoh, Yoshiyuki Hanaoka, Katsuhiro Kobayashi, Makio Oka, Takashi Shibata, Tomoyuki Akiyama, Yumiko Hayashi
Publikováno v:
Epilepsia Open
Summary We investigated the relationship between the scalp distribution of fast (40–150 Hz) oscillations (FOs) and epileptogenic lesions in West syndrome (WS) and related disorders. Subjects were 9 pediatric patients with surgically confirmed struc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e3eb43427472bd0b89c1dab2e16f18e
http://europepmc.org/articles/PMC5719855
http://europepmc.org/articles/PMC5719855
Autor:
Makio Oka, Harumi Yoshinaga, Mamoru Ouchida, Yoshiyuki Hanaoka, Toshiyuki Yamamoto, Tomoyuki Akiayma, Yoshinori Kobayashi, Katsuhiro Kobayashi, Iori Ohmori
Publikováno v:
Brain and Development. 39:75-79
We report a female patient with Dravet syndrome (DS) with erratic segmental myoclonus, the origin of which was first identified in the cerebral cortex by the detection of myoclonus-associated cortical discharges. The discharges were disclosed through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84473327e099ad66f215bc17946b5e93
https://doi.org/10.1016/j.braindev.2016.07.005
https://doi.org/10.1016/j.braindev.2016.07.005
Autor:
Takao Yasuhara, Yoshiyuki Hanaoka, S. Sato, Keiko Shimojima, Katsuhiro Kobayashi, Toshiyuki Yamamoto, Harumi Yoshinaga, Makio Oka
Publikováno v:
Clinical Genetics. 89:739-743
The p.Asp211Gly homozygous HYLS1 mutation is so far known to cause only hydrolethalus syndrome, a lethal malformation syndrome. We report living sibling patients with a homozygous no-stop mutation in exon 4 of HYLS1, NM_145014.2:c.900A>C (p.Ter300Tyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be5d9502920e1efd76550e44e1a77e67
https://doi.org/10.1111/cge.12752
https://doi.org/10.1111/cge.12752