Zobrazeno 1 - 10
of 375
pro vyhledávání: '"Sachio, Takashima"'
Autor:
Sachiko Iwata, Reiji Katayama, Kennosuke Tsuda, Yung‐Chieh Lin, Tsuyoshi Kurata, Masahiro Kinoshita, Koya Kawase, Takenori Kato, Shin Kato, Tadashi Hisano, Motoki Oda, Etsuko Ohmae, Sachio Takashima, Yuko Araki, Shinji Saitoh, Osuke Iwata
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 9, Pp 1417-1427 (2022)
Abstract Objective MRI provides useful information regarding brain maturation and injury in newborn infants. However, MRI studies are generally restricted during acute phase, resulting in uncertainty around upstream clinical events responsible for su
Externí odkaz:
https://doaj.org/article/47a8ba50a619484e95f15b375d88efe4
Autor:
Osuke Iwata, Sachiko Iwata, Tsuyoshi Kurata, Kennosuke Tsuda, Koya Kawase, Masahiro Kinoshita, Yung-Chieh Lin, Mamoru Saikusa, Yuko Araki, Sachio Takashima, Motoki Oda, Etsuko Ohmae, Shiji Saitoh
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract If the brain structure is assessed at neonatal intensive care units, covert clinical events related with subtle brain injury might be identified. The reduced scattering coefficient of near-infrared light (μS’) obtained using time-resolved
Externí odkaz:
https://doaj.org/article/9bd4cf2a1f284833aa8da935aea17999
Autor:
Eiko Takeshita, Sachio Takashima, Masayuki Nakashima, Hiromi Ishibashi, Yoriko Watanabe, Toshio Hanai, Mayumi Matsufuji, Kaori Fukui
Publikováno v:
Brain and Development. 42:231-235
An adult female patient was diagnosed with arginase 1 deficiency (ARG1-D) at 4 years of age, and had been managed with protein restriction combined with sodium benzoate therapy. Though the treatment was successful in ameliorating hyperammonemia, hype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68c01752e0c71bd45e5efdf969808be4
https://doi.org/10.1016/j.braindev.2019.09.002
https://doi.org/10.1016/j.braindev.2019.09.002
Autor:
Hiroyuki Sano, Akihito Takahashi, Masanori Tamura, Takuya Tokuhisa, Nanae Yutaka, Satoshi Osaga, Akihito Takeuchi, Takeo Mukai, Jun Shibasaki, Tomoaki Ioroi, Toshiki Takenouchi, Makoto Nabetani, Kennosuke Tsuda, Sachiko Iwata, Sachio Takashima, Hisanori Sobajima, Osuke Iwata, Shigeharu Hosono
Publikováno v:
Therapeutic Hypothermia and Temperature Management
Therapeutic hypothermia following neonatal encephalopathy is neuroprotective. However, approximately one in two cooled infants still die or develop permanent neurological impairments. Further understanding of variables associated with the effectivene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396f53d6c7713cf2e5c1473787ec2607
https://doi.org/10.1089/ther.2018.0019
https://doi.org/10.1089/ther.2018.0019
Publikováno v:
Rigakuryoho Kagaku. 34:125-129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::936153ee05f2bfaff64cede083b1bdfd
https://doi.org/10.1589/rika.34.125
https://doi.org/10.1589/rika.34.125
Autor:
Etsuko Ohmae, Yung Chieh Lin, Yuko Araki, Sachiko Iwata, Koya Kawase, Kennosuke Tsuda, Tsuyoshi Kurata, Masahiro Kinoshita, Mamoru Saikusa, Osuke Iwata, Shiji Saitoh, Sachio Takashima, Motoki Oda
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
If the brain structure is assessed at neonatal intensive care units, covert clinical events related with subtle brain injury might be identified. The reduced scattering coefficient of near-infrared light (μS’) obtained using time-resolved near-inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14b7aea50979504efb175c10033b0141
https://pubmed.ncbi.nlm.nih.gov/34716370
https://pubmed.ncbi.nlm.nih.gov/34716370
Autor:
Yushiro Yamashita, Sachio Takashima, Naoko Hara, Mamoru Saikusa, Ryota Shindou, Shinji Saitoh, Masahiro Kinoshita, Kennosuke Tsuda, Eimei Harada, Osuke Iwata, Teiko Yoshizuka, Sachiko Iwata, Nobuyuki Takeshige, Takenori Kato
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
For infants with acute progressive hydrocephalus, invasive drainage of cerebrospinal fluid (CSF) is performed until a ventriculo-peritoneal shunt can be inserted. Surrogate markers of intracranial pressure (ICP) may help optimise the timing of invasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a044c3fe0daeec124ef11f43fa73ebab
https://doi.org/10.1038/s41598-018-30274-3
https://doi.org/10.1038/s41598-018-30274-3
Autor:
Dawna D. Armstrong, Kanehiro Hayashi, Ken Inoue, Masahiro Nakayama, Yukio Hirata, Kohichi Tanaka, Kiyofumi Yamada, Minkyung Shin, Barbara Antalffy, Sachio Takashima, Kazuhiro Ishii, Ayako Kitazawa, Toshihiro Endo, Masaki Kakeyama, Wei Shan, Taku Nagai, Yuki Matsunaga, Seico Benner, Ken Ichiro Kubo, Yukiko Ito, Kenji F. Tanaka, Kimiko Deguchi, Keitaro Yoshida, Kazunori Nakajima, Michihiko Aramaki, Masayuki Itoh, Chiharu Tohyama
Publikováno v:
JCI Insight. 2
Many extremely preterm infants (born before 28 gestational weeks [GWs]) develop cognitive impairment in later life, although the underlying pathogenesis is not yet completely understood. Our examinations of the developing human neocortex confirmed th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45af9e99343cc985798f26dc74fb3d90
https://doi.org/10.1172/jci.insight.88609
https://doi.org/10.1172/jci.insight.88609
Autor:
Miwa Sohda, Naoto Kakinuma, Shinya Ueno, Yoshiko Haga, Kazuyoshi Watanabe, Shinichi Hirose, Yoshio Misumi, Bo Zhang, Sen Takeda, Atsushi Ishii, Takeshi Kanaumi, Motohiro Okada, Sachio Takashima, Sunao Kaneko
Publikováno v:
Epilepsy Research. 108:420-432
Mutations in GABRG2, which encodes the γ2 subunit of GABAA receptors, can cause both genetic epilepsy with febrile seizures plus (GEFS+) and Dravet syndrome. Most GABRG2 truncating mutations associated with Dravet syndrome result in premature termin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e1c876bb4df9bb45f3fdf1bf65ef86
https://doi.org/10.1016/j.eplepsyres.2013.12.005
https://doi.org/10.1016/j.eplepsyres.2013.12.005
Publikováno v:
Pediatric Neurology. 49:477-481
Background Proteolipid protein 1 gene ( PLP1 ) mutations result in a continuum of neurological findings characterized by X-linked hypomyelinating leukodystrophies of the central nervous system, from mild spastic paraplegia type 2 to severe Pelizaeus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da7cbed63a079765bc93bb907ea48b69
https://doi.org/10.1016/j.pediatrneurol.2013.07.012
https://doi.org/10.1016/j.pediatrneurol.2013.07.012