Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Shinji Saitoh"'
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
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
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:
Mayu Fujikawa, Yurika Numata-Uematsu, Takashi Shiihara, Mitsugu Uematsu, Tomoko Kobayashi, Shinji Saitoh, Ayako Hattori, Noriko Togashi, Kei Ohashi, Shigeo Kure, Yu Aihara
Publikováno v:
Epilepsybehavior : EB. 111
Background Tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND) have a large impact on patients and their families. Improving intellectual ability outcomes using preventive vigabatrin (VGB) treatment has recently been reporte
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:
Misa Miyake, Shinji Saitoh, Satoru Kobayashi, Takeshi Tsuji, Tetsushi Yoshikawa, Kazuto Ueda, Yoshiyuki Takahashi, Michio Suzuki, Ikumi Hori, Akihisa Okumura, Hirokazu Kurahashi, Jun Natsume, Erina Kataoka
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 61(9)
Background Few population-based surveys of childhood arterial ischemic stroke (AIS) have been conducted in Asian countries. The aim of this study was to investigate the clinical features, time to diagnosis, and prognosis of childhood AIS in a populat
Autor:
Mitsuhiro Kato, Yasuhiro Suzuki, Kenjiro Kosaki, Shinji Saitoh, Mami Yamasaki, Yoshikazu Hatsukawa, Fuyuki Miya, Nobuhiko Okamoto, Tatsuhiko Tsunoda, Yuto Yamamoto, Yonehiro Kanemura, Kazumi Kawato
Publikováno v:
Journal of Human Genetics. 62:927-929
Inherited optic neuropathies (IONs) are neurodegenerative disorders affecting the optic nerve and the nervous system. Dominant and recessive IONs are known. Many of the dominant IONs are caused by mutations of OPA1. Autosomal-recessive IONs are rare.