Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Hideto, Nakao"'
Autor:
Shoko Tamaki, Sota Iwatani, Ayako Izumi, Kentaro Hirayama, Dai Kataoka, Shohei Ohyama, Toshihiko Ikuta, Emiko Takeoka, Sachiko Matsui, Hitomi Mimura, Shogo Minamikawa, Yasuo Nakagishi, Seiji Yoshimoto, Hideto Nakao
Publikováno v:
American Journal of Medical Genetics Part A. 188:1048-1055
The effects of medical and surgical interventions on the survival of patients with trisomy 18 have been reported, leading to changes in perinatal management and decision-making. However, few studies have fully reported the recent changes in survival
Autor:
Sota Iwatani, Yuko Murakami, Masami Mizobuchi, Kazumichi Fujioka, Keiko Wada, Hitomi Sakai, Seiji Yoshimoto, Hideto Nakao
Publikováno v:
American Journal of Perinatology Reports, Vol 4, Iss 01, Pp 005-008 (2014)
Abstract Congenital candidiasis, which presents with a variety of clinical symptoms, is very rare in both term and preterm infants, and less than 100 neonatal cases have been reported in the medical literature. We describe the case of an extremely pr
Externí odkaz:
https://doaj.org/article/913ec27d3ead4ff89db90310b1ad8754
Autor:
Miwa Yamamoto, Hideto Nakao, Takao Kobayashi, Akihiro Hirata, Makiko Yoshida, Sota Iwatani, Sachiko Matsui, Seiji Yoshimoto
Publikováno v:
American Journal of Perinatology. 39:0987-0994
Objective The fetal inflammatory response syndrome (FIRS) is characterized by elevated concentrations of inflammatory cytokines in fetal blood, with preterm delivery and morbidity. Umbilical cord serum interleukin-6 (UC-s-IL-6) is an ideal marker for
Autor:
Sota Iwatani, Kazuya Uemura, Masami Mizobuchi, Seiji Yoshimoto, Keiichiro Kawasaki, Yoshiyuki Kosaka, Masayuki Hori, Takahiro Yasumi, Hideto Nakao
Publikováno v:
American Journal of Perinatology Reports, Vol 05, Iss 01, Pp e22-e24 (2015)
Abstract Background Familial hemophagocytic lymphohistiocytosis (FLH) is an autosomal recessive disorder of immune regulation that leads to a hyperinflammatory syndrome. Fetal onset FHL is extremely rare and is considered to be the most severe form
Externí odkaz:
https://doaj.org/article/38c06ceffc3443c6a993df5a3aeec1fb
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(8)
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 62(10)
Autor:
Nanako Nino, Hideto Nakao, Atsuro Saito, Saki Okubo, Kenji Kishimoto, Makiko Yoshida, Akihiro Tamura, Toshiaki Ishida, Yoshiyuki Kosaka, Teppei Tahara, Seiji Yoshimoto, Takehito Yokoi, Suguru Uemura, Keiichiro Kawasaki, Daiichiro Hasegawa
Publikováno v:
International Journal of Hematology. 106:711-717
Congenital pure erythroid leukemia is exceedingly rare and poses a diagnostic challenge. We report an atypical case of congenital pure erythroid leukemia that did not express typical erythroid markers. The patient presented with a high white blood ce
Publikováno v:
Congenital Anomalies. 57:201-204
There have been several reports on 5q31.3 microdeletion syndrome. The overlapping deleted region includes purine-rich element binding protein A (PURA), which encodes transcriptional activator protein Pur-α. Patients with PURA mutations show moderate
Autor:
Hideto Nakao, Masami Mizobuchi, Miho Nagasawa, Takefumi Kikusui, Keiko Wada, Seiji Yoshimoto, Hitomi Sakai, Hiroshi Yamaguchi
Publikováno v:
Neonatology. 109:228-234
Background: Some prior studies have shown that symptomatic patent ductus arteriosus (sPDA) is highly familial. Although it is estimated that both genetic and environmental factors may contribute to sPDA, evidence is still lacking. Objective: The aim
Autor:
Masami Mizobuchi, Hideto Nakao, Satoshi Tanaka, Seiji Yoshimoto, Hitomi Sakai, Sota Iwatani, Kei Inomata
Publikováno v:
Pediatrics International. 56:851-855
Background The aim of this study was to determine whether patterns of increases in serum interleukin-6 (IL-6) and C-reactive protein (CRP) levels at birth were associated with the development of white matter injury (WMI) in preterm infants with a fet