Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Hiroyuki, Iijima"'
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract The effectiveness of patent foramen ovale closure for migraine has been previously discussed. By contrast, very few studies have reported the association between migraine and atrial septal defect closure. Here, we report a case in which atri
Externí odkaz:
https://doaj.org/article/7bfa1c84e0e243a0902258f4116271ca
Autor:
Sonoko Minato, Hiroyuki Iijima, Hiro Nakao, Kentaro Nishi, Yoshihiko Hidaka, Norimitsu Inoue, Mitsuru Kubota, Akira Ishiguro
Publikováno v:
Immunological Medicine, Vol 44, Iss 4, Pp 274-277 (2021)
Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by overactivation of the complement alternative pathway. aHUS involves the presence of antibodies against complement factor H and its mutations in the complement genes. A 2-month-old
Externí odkaz:
https://doaj.org/article/eb0986792db5432d9921ceb1aa550f27
Autor:
Haruka Fukayama, Kensuke Shoji, Michiko Yoshida, Hiroyuki Iijima, Takanobu Maekawa, Akira Ishiguro, Isao Miyairi
Publikováno v:
IDCases, Vol 27, Iss , Pp e01406- (2022)
The Streptococcus mitis group constitutes a part of the oral flora in humans and has been reported to cause infective endocarditis, brain abscesses, sepsis, pneumonia, and peritonitis. However, the S. mitis group rarely causes meningitis in children.
Externí odkaz:
https://doaj.org/article/c41e4c30129848f2bb787f60ee57021d
Autor:
Jun Kido, Shirou Matsumoto, Eiko Takeshita, Chiemi Hayakawa, Keitaro Yamada, Jiro Kagawa, Yoko Nakajima, Tetsuya Ito, Hiroyuki Iijima, Fumio Endo, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100805- (2021)
Arginase 1 (ARG1) deficiency is a rare urea cycle disorder (UCD), with an estimated frequency of 1 per 2,200,000 births in Japan. Patients with ARG1 deficiency develop symptoms in late infancy or pre-school age with progressive neurological manifesta
Externí odkaz:
https://doaj.org/article/c4b22b71401143fe8b39cc0b21142d7c
Autor:
Ikumi Sako, Hiroyuki Iijima, Toshihiro Matsui, Kensuke Shoji, Takashi Ishikawa, Akira Ishiguro
Publikováno v:
Clinical Case Reports, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Osteomyelitis in childhood is often hematogenous and neonates are generally prone to bacteremia because of immature immunity. Neonatal osteomyelitis occurs even in the absence of apparent immunological or perinatal abnormalities.
Externí odkaz:
https://doaj.org/article/97bdb60ac2ae43ce8a7673c4d394274b
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100702- (2021)
Background: Glycogen storage disease type 0a (GSD 0a), caused by GYS2 mutations, has a broad phenotypic spectrum, mostly associated with hypoglycemia. This disease has been characterized by the inability to store glycogen in the liver, leading to no
Externí odkaz:
https://doaj.org/article/d8d85e0b907349dc87ecee49437a455f
Autor:
Hiroyuki Iijima, Reiko Iwano, Yukichi Tanaka, Koji Muroya, Tokiko Fukuda, Hideo Sugie, Kenji Kurosawa, Masanori Adachi
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 17, Iss , Pp 31-37 (2018)
Background: Glycogen storage disease type IV (GSD IV), caused by GBE1 mutations, has a quite wide phenotypic variation. While the classic hepatic form and the perinatal/neonatal neuromuscular forms result in early mortality, milder manifestations inc
Externí odkaz:
https://doaj.org/article/406a2551d3c14318bb5f5c68b8dce284
Clinical characteristics of pediatric patients with COVID-19 between Omicron era vs. pre-Omicron era
Publikováno v:
Journal of Infection and Chemotherapy. 28:1501-1505
Detailed data on clinical characteristics in children with the omicron strain of SARS-COV-2 are limited.We conducted a retrospective observational study of children with COVID-19 at the National Center for Child Health and Development to evaluate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::608080b1740dd704e530d698130000f2
https://doi.org/10.1016/j.jiac.2022.07.016
https://doi.org/10.1016/j.jiac.2022.07.016
Autor:
Kenji Yamashiro, Keisuke Mori, Shigeru Honda, Mariko Kano, Yasuo Yanagi, Akira Obana, Yoichi Sakurada, Taku Sato, Yoshimi Nagai, Taiichi Hikichi, Yasushi Kataoka, Chikako Hara, Yasurou Koyama, Hideki Koizumi, Munemitsu Yoshikawa, Masahiro Miyake, Isao Nakata, Takashi Tsuchihashi, Kuniko Horie-Inoue, Wataru Matsumiya, Masashi Ogasawara, Ryo Obata, Seigo Yoneyama, Hidetaka Matsumoto, Masayuki Ohnaka, Hirokuni Kitamei, Kaori Sayanagi, Sotaro Ooto, Hiroshi Tamura, Akio Oishi, Sho Kabasawa, Kazuhiro Ueyama, Akiko Miki, Naoshi Kondo, Hiroaki Bessho, Masaaki Saito, Hidenori Takahashi, Xue Tan, Keiko Azuma, Wataru Kikushima, Ryo Mukai, Akihiro Ohira, Fumi Gomi, Kazunori Miyata, Kanji Takahashi, Shoji Kishi, Hiroyuki Iijima, Tetsuju Sekiryu, Tomohiro Iida, Takuya Awata, Satoshi Inoue, Ryo Yamada, Fumihiko Matsuda, Akitaka Tsujikawa, Akira Negi, Shin Yoneya, Takeshi Iwata, Nagahisa Yoshimura
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract We conducted a genome-wide association study (GWAS) on the outcome of anti-VEGF treatment for exudative age-related macular degeneration (AMD) in a prospective cohort. Four hundred and sixty-one treatment-naïve AMD patients were recruited a
Externí odkaz:
https://doaj.org/article/bc91a8dbe7224475a7ce9c259ddea49c
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. 11:514-517
In this single-center retrospective observational study, we report that the incidence of seizures in febrile children with COVID-19 was significantly higher in the Omicron era than in the pre-Omicron era (14.6% vs 1.7%, P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fdf5f3da9cd4d3e0beba553d09f8f1a
https://doi.org/10.1093/jpids/piac085
https://doi.org/10.1093/jpids/piac085