Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Shinji Saitoh"'
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:
Kazunori Imai, Kohei Aoyama, Takato Goto, Tamao Kitaori, Toshiyuki Iguchi, Hiroshi Sasano, Tomonori Hattori, Mayumi Sugiura‐Ogasawara, Shinji Saitoh
Publikováno v:
Acute Medicine & Surgery, Vol 10, Iss 1, Pp n/a-n/a (2023)
Background Hematocolpos due to imperforate hymen is an important differential diagnosis of abdominal pain in early adolescent stage. However, hematocolpos due to lower vaginal agenesis must be considered because the management differs. Case Presentat
Externí odkaz:
https://doaj.org/article/c4c30227f91842169e002876bf79c8b6
Autor:
Hirofumi Komaki, Yoshihiro Maegaki, Tsuyoshi Matsumura, Kazuhiro Shiraishi, Hiroyuki Awano, Akinori Nakamura, Satoru Kinoshita, Katsuhisa Ogata, Keiko Ishigaki, Shinji Saitoh, Michinori Funato, Satoshi Kuru, Takahiro Nakayama, Yasuyuki Iwata, Hiroyuki Yajima, Shin’ichi Takeda
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 2, Pp 181-190 (2020)
Abstract 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 patholo
Externí odkaz:
https://doaj.org/article/001a1b84c3124cd5bcf321aa65fa9301
Autor:
Takuya Hiraide, Ayako Hattori, Daisuke Ieda, Ikumi Hori, Shinji Saitoh, Mitsuko Nakashima, Hirotomo Saitsu
Publikováno v:
Epilepsia Open, Vol 4, Iss 3, Pp 476-481 (2019)
Abstract Epilepsy with myoclonic absences is a specific seizure type characterized by bilateral rhythmic clonic jerks with impairment of consciousness. Here, we report an individual with epilepsy with myoclonic absences, mild intellectual disabilitie
Externí odkaz:
https://doaj.org/article/3e3682cd96a447f084c142007ca0e052
Autor:
Yuta Inoue, Naomi Tsuchida, Nobuhiko Okamoto, Shimakawa Shuichi, Kei Ohashi, Shinji Saitoh, Atsushi Ogawa, Keisuke Hamada, Masamune Sakamoto, Noriko Miyake, Kohei Hamanaka, Atsushi Fujita, Eriko Koshimizu, Satoko Miyatake, Takeshi Mizuguchi, Kazuhiro Ogata, Yuri Uchiyama, Naomichi Matsumoto
Publikováno v:
Clinical Genetics. 103:590-595
AFF3 at 2q11.2 encodes the nuclear transcriptional activator AF4/FMR2 Family Member 3. AFF3 constitutes super elongation complex like 3, which plays a role in promoting the expression of genes involved in neurogenesis and development. The degron moti
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:
Akiko Tamasaki, Ikumi Hori, Masayoshi Oguri, Hiroyuki Yamada, Yoshihiro Maegaki, Shinji Saitoh
Publikováno v:
Yamada Hiroyuki, Tamasaki Akiko, Oguri Masayoshi, et al. Frequent epileptic apnoea in a patient with Pitt-Hopkins syndrome. EPILEPTIC DISORDERS. 2020. 22(5). 673-677. doi:10.1684/epd.2020.1212
Pitt-Hopkins syndrome is a rare genetic disease, characterised by severe intellectual disability, distinctive dysmorphic features, epilepsy and distinctive breathing abnormalities during wakefulness. Here, we describe the case of a 22-year-old woman
Publikováno v:
Nihon Kyukyu Igakukai Zasshi: Journal of Japanese Association for Acute Medicine. 31:345-352
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