Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Shinji Saitoh"'
Publikováno v:
International Journal of Developmental Neuroscience. 82:188-195
To investigate the diagnostic rate of autism spectrum disorder (ASD) in a high-survival cohort of very preterm children, 77 infants born very preterm (32 weeks of gestation) were assessed at age 4-6 years old using the Autism Diagnostic Observation S
Autor:
Kiyokuni Miura, Tetsushi Yoshikawa, Shinji Saitoh, Masaharu Noda, Mihoko Mizuno, Atsuko Ohno, Yoshiyuki Takahashi, Jun Natsume, Atsushi Numaguchi, Akihisa Okumura
Publikováno v:
Pediatric Research
Background Children receiving home medical care need special attention to prevent unexpected death. The aim of this study was to clarify the factors contributing to death in children receiving home medical care from the child death review database. M
Autor:
Naomi Kawaoka, Tomoko Asai, Masayuki Imaeda, Shinji Saitoh, Satomi Fukuhara, Taishi Miyachi, Kei Ohashi
Publikováno v:
Journal of Autism and Developmental Disorders
In March 2020, many schools were closed to prevent the spread of COVID-19 in Japan, and it is predicted that many children, especially those with neurodevelopmental disorders (NDDs), will be affected emotionally and behaviorally. Here, we examined th
Autor:
Masamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, Akihiko Ishiyama, Hirofumi Komaki, Takashi Saito, Eri Takeshita, Yuko Shimizu-Motohashi, Kazuhiro Haginoya, Tomoko Kobayashi, Tomohide Goto, Yu Tsuyusaki, Mizue Iai, Kenji Kurosawa, Hitoshi Osaka, Jun Tohyama, Yu Kobayashi, Nobuhiko Okamoto, Yume Suzuki, Satoko Kumada, Kenji Inoue, Hideaki Mashimo, Atsuko Arisaka, Ichiro Kuki, Harumi Saijo, Kenji Yokochi, Mitsuhiro Kato, Yuji Inaba, Yuko Gomi, Shinji Saitoh, Kentaro Shirai, Masafumi Morimoto, Yuishin Izumi, Yoriko Watanabe, Shin-ichiro Nagamitsu, Yasunari Sakai, Shinobu Fukumura, Kazuhiro Muramatsu, Tomomi Ogata, Keitaro Yamada, Keiko Ishigaki, Kyoko Hirasawa, Konomi Shimoda, Manami Akasaka, Kosuke Kohashi, Takafumi Sakakibara, Masashi Ikuno, Noriko Sugino, Takahiro Yonekawa, Semra Gürsoy, Tayfun Cinleti, Chong Ae Kim, Keng Wee Teik, Chan Mei Yan, Muzhirah Haniffa, Chihiro Ohba, Shuuichi Ito, Hirotomo Saitsu, Ken Saida, Naomi Tsuchida, Yuri Uchiyama, Eriko Koshimizu, Atsushi Fujita, Kohei Hamanaka, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Noriko Miyake, Naomichi Matsumoto
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(12)
Cerebellar hypoplasia and atrophy (CBHA) in children is an extremely heterogeneous group of disorders, but few comprehensive genetic studies have been reported. Comprehensive genetic analysis of CBHA patients may help differentiating atrophy and hypo
Autor:
Farnaz Hosseini Beheshti, Noriko Miyake, Shermineh Heydari, Jafar Nasiri, Shinji Saitoh, Ahmad Reza Salehi Chaleshtori, Naomichi Matsumoto, Kohei Hamanaka, Atsushi Takata, Masoud Garshasbi
Publikováno v:
Journal of Human Genetics. 66:445-448
Intellectual disability (ID) accounts for 1% of the general population, and it is caused by the interplay between the genetic and/or environmental factors. The genetic components responsible for the development of ID are highly heterogeneous, and the
Autor:
Tetsushi Yoshikawa, Toshiyuki Fukao, Yoshiyuki Takahashi, Hirokazu Kurahashi, Shinji Saitoh, Hideyuki Iwayama, Masahiro Hirayama, Jun Natsume, Shingo Numoto, Akihisa Okumura
Publikováno v:
Pediatrics International. 62:337-340
Background An outbreak of acute flaccid myelitis was chronologically correlated with an outbreak of severe respiratory illness in Japan in 2015. We hypothesized that increases in children hospitalized with severe respiratory illnesses might also be a
Autor:
Yasuyuki Iwata, Katsuhisa Ogata, Keiko Ishigaki, Tsuyoshi Matsumura, Hiroyuki Awano, Shin'ichi Takeda, Akinori Nakamura, Michinori Funato, Satoshi Kuru, Hirofumi Komaki, Satoru Kinoshita, Shinji Saitoh, Hiroyuki Yajima, Yoshihiro Maegaki, Kazuhiro Shiraishi, T. Nakayama
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 2, Pp 181-190 (2020)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective Duchenne muscular dystrophy (DMD) is a progressive muscular disease characterized by chronic cycles of inflammatory and necrotic processes. Prostaglandin D2 (PGD2) is produced by hematopoietic PGD synthase (HPGDS), which is pathologically i
Autor:
Takeshi Ebara, Hazuki Tamada, Sayaka Kato, Mayumi Sugiura-Ogasawara, Hirohisa Kano, Michihiro Kamijima, Yasuyuki Yamada, Hirotaka Sato, Shinji Saitoh, Taro Matsuki
Publikováno v:
International Journal of Environmental Research and Public Health, Vol 18, Iss 11373, p 11373 (2021)
International Journal of Environmental Research and Public Health
Volume 18
Issue 21
International Journal of Environmental Research and Public Health
Volume 18
Issue 21
To discuss appropriate physical activity (PA) levels during pregnancy, this prospective cohort study examined the relationships between PA levels before and during pregnancy and physical and mental health status. Fixed data for 104,102 pregnant women
Autor:
Akira Kinoshita, Tatsuya Kishino, Ryoichi Mori, Naoko Asahina, Yutaka Negishi, Hideaki Shiraishi, Kana Hosoki, Koh-ichiro Yoshiura, Masahiro Nakashima, Kiyotaka Tomiwa, Katsuya Matsuda, Shinji Saitoh, Hiroyuki Mishima, Naoko Ishihara, Susumu Tanimura, Kaname Ohyama
Publikováno v:
Development. 148
Mutations in ITPR1 cause ataxia and aniridia in individuals with Gillespie syndrome (GLSP). However, the pathogenic mechanisms underlying aniridia remain unclear. We identified a de novo GLSP mutation hotspot in the 3′-region of ITPR1 in five indiv
Autor:
Ayano Otani-Matsuura, Mayumi Sugiura-Ogasawara, Takeshi Ebara, Taro Matsuki, Hazuki Tamada, Yasuyuki Yamada, Toyonori Omori, Sayaka Kato, Hirohisa Kano, Kayo Kaneko, Kazuki Matsuzaki, Shinji Saitoh, Michihiro Kamijima
Publikováno v:
Journal of Reproductive Immunology. 152:103659
There are a limited number of studies in which the depression status was followed up throughout pregnancy and postpartum to 1 year after delivery though 8.6-33% of women with recurrent pregnancy loss (RPL) and 10-25% of women who undergo in vitro fer