Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Shinji Saitoh"'
Autor:
Sachiko Iwata, Shin Kato, Tadashi Hisano, Yuko Mizutani, Osuke Iwata, Satoko Fukaya, Yung Chieh Lin, Koya Kawase, Shinji Saitoh, Masahiro Kinoshita
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss, Pp S10-S15 (2021)
Despite the increased survival opportunities for extremely preterm infants, their long-term cognitive outcomes remain poor, with increased incidence of cognitive impairments in childhood and reduced opportunities to attend higher education in young a
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
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:
Takeshi Ebara, Taro Matsuki, Yasuyuki Yamada, Michihiro Kamijima, Mayumi Sugiura-Ogasawara, Toyonori Omori, Nobuhiro Suzumori, Sayaka Kato, Shinji Saitoh
Publikováno v:
Birth (Berkeley, Calif.)
Background The work patterns of pregnant women may be related to adverse obstetric and perinatal outcomes. This study aimed to clarify the effects of weekly working time according to frequencies of night shifts during pregnancy on adverse outcomes in
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:
Nobuhiro, Suzumori, Takeshi, Ebara, Hazuki, Tamada, Taro, Matsuki, Hirotaka, Sato, Sayaka, Kato, Shinji, Saitoh, Michihiro, Kamijima, Mayumi, Sugiura-Ogasawara, Takahiko, Katoh
Publikováno v:
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-9 (2021)
Background Postpartum depression is one of the most commonly experienced psychological disorders for women after childbirth, usually occurring within one year. This study aimed to clarify whether women with delivery with anesthesia, including epidura
Publikováno v:
Braindevelopment. 43(4)
Introduction Angelman syndrome (AS) and Prader-Willi syndrome (PWS) are neurodevelopmental disorders caused by loss of function of maternally expressed UBE3A and paternally expressed contiguous genes on chromosome 15q11-13, respectively. A majority o
Autor:
Tatsuo Akechi, Iori Sato, Yoshimi Takeda, Yuji Ishida, Shinji Saitoh, Masaki Kondo, Yuka Kato, Michi Kamei, Akemi Tsumura, Yoshinori Ito, Toru Okuyama
Publikováno v:
Japanese journal of clinical oncology. 50(3)
Background Patients with childhood cancer and their families frequently experience psychosocial distress associated with cancer and its treatment. We thus examined the reliability and validity of a Japanese version of the Psychosocial Assessment Tool
Autor:
Shinji Saitoh, Akie Nakamura, Reiko Horikawa, Maki Fukami, Tohru Yorifuji, Rika Kosaki, Keisuke Nagasaki, Tsutomu Ogata, Keiko Matsubara, Seiji Mizuno, Chikahiko Numakura, Masayo Kagami, Yasuhiro Naiki, Toshihiro Tajima
Publikováno v:
Genetics in Medicine
Purpose Temple syndrome (TS14) is a rare imprinting disorder caused by aberrations at the 14q32.2 imprinted region. Here, we report comprehensive molecular and clinical findings in 32 Japanese patients with TS14. Methods We performed molecular studie
Autor:
Naoko Oya, Atsuko Nakagawa, Naoto Shoji, Masayo Kojima, Takeshi Ebara, Sayaka Kato, Yasuyuki Yamada, Shinji Saitoh, Taro Matsuki, Yasuhiko Ozaki, Jun Ueyama, Taishi Miyachi, Mayumi Sugiura-Ogasawara, Tomoko Oguri, Toyonori Omori, Yuki Ito, Motohiro Tomizawa, Michihiro Kamijima, Sadao Suzuki, Hirotaka Sato
Publikováno v:
BMJ Open
PurposeEffects of fetal, perinatal and childhood environment on the health of children at birth and during later life have become a topic of concern. The Aichi regional sub-cohort of the Japan Environment and Children’s Study (JECS-A) is an ongoing