Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Hideki Horita"'
Publikováno v:
JMIR Pediatrics and Parenting, Vol 5, Iss 4, p e35466 (2022)
BackgroundParents of adolescents with internet addiction are confronted with their children’s internet problems on a daily basis. Parents may notice that adolescents with addiction may also have emotional and behavioral problems, including impulsiv
Externí odkaz:
https://doaj.org/article/96f573946a4043baad938f46d3028817
BACKGROUND Background: Parents of adolescents with Internet addiction are confronted with their children' Internet problems on a daily basis. Parents may notice that adolescents with addiction may also have emotional and behavioral problems including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14a4ba199f6991661bf4b352286f37e0
https://doi.org/10.2196/preprints.35466
https://doi.org/10.2196/preprints.35466
Publikováno v:
JMIR Pediatrics & Parenting; Oct-Dec2022, Vol. 5 Issue 4, p1-11, 11p
Autor:
Hitoshi Osaka, Noriko Miyake, Kiyomi Nishiyama, Hideki Horita, Yuriko Yoneda, Mitsuhiro Kato, Kiyoshi Hayasaka, Naomichi Matsumoto, Yukiko Kondo, Hiroshi Doi, Hirotomo Saitsu, Nobuko Moriyama, Yoshinori Tsurusaki
Publikováno v:
Epilepsia. 53:1441-1449
Summary Purpose: Ohtahara syndrome (OS) is one of the most severe and earliest forms of epilepsy. STXBP1 and ARX mutations have been reported in patients with OS. In this study, we aimed to identify new genes involved in OS by copy number analysis an
Autor:
Hirotomo, Saitsu, Mitsuhiro, Kato, Hitoshi, Osaka, Nobuko, Moriyama, Hideki, Horita, Kiyomi, Nishiyama, Yuriko, Yoneda, Yukiko, Kondo, Yoshinori, Tsurusaki, Hiroshi, Doi, Noriko, Miyake, Kiyoshi, Hayasaka, Naomichi, Matsumoto
Publikováno v:
Epilepsia. 53(8)
Ohtahara syndrome (OS) is one of the most severe and earliest forms of epilepsy. STXBP1 and ARX mutations have been reported in patients with OS. In this study, we aimed to identify new genes involved in OS by copy number analysis and whole exome seq
Publikováno v:
Pediatric Neurology. 9:435-443
Diaschisis is a functional impairment at a site in the brain remote from the lesion causing it. An investigation of cerebellar diaschisis in childhood was undertaken to better understand the functional maturation of the corticopontocerebellar tract i
Publikováno v:
Journal of the Japan Epilepsy Society. 9:63-66
脳波上, 後頭部と前頭極部にほぼ同期した棘波もしくは棘徐波 (O, Fp棘波) をみる25例を対象とした。調査時年齢は平均10歳5ヵ月であった。臨床診断は, てんかん19例, 熱性痙攣4例などで, て
Autor:
Hideki Horita, Manabu Tanaka, Takahiro Nara, Yoshikatsu Eto, Shin-ichiro Hamano, Saburo Kohno, Sakiko Kawasaki
Publikováno v:
Pediatric neurology. 23(3)
West syndrome, although classified as a generalized epilepsy, is associated with localized cerebral lesions in some cases. However, similar localized cortical abnormalities usually can result in partial epilepsy, instead of West syndrome. We performe
Publikováno v:
Physica B: Condensed Matter. :1083-1084
de Haas–van Alphen (dHvA) effect in anti-ferromagnetic state of SmCu 2 has been performed in the field up to 12 T and at temperature down to 0.4 K. At least 24 branches with the frequencies from 1.2 to 46 MG have been found. The cyclotron effective
Autor:
Hideki Horita
Publikováno v:
Psychiatry and Clinical Neurosciences. 55:171-172
The subjects were 25 children, including West syndrome, Lennox-Gastaut syndrome, childhood absence epilepsy (CAE) and localization-related epilepsies. Clinical seizures occurred only during waking state in 14 patients (including the cases of West syn