Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Toru Yoneda"'
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Muckle-Wells syndrome (MWS) is an autosomal dominant autoinflammatory disease recognized as the intermediate phenotype of cryopyrin-associated periodic syndrome (CAPS) caused by NLRP3 gene mutation. It often takes a long time before the diagnosis is
Externí odkaz:
https://doaj.org/article/4f323d73eb5648b4ada096436f09dc97
Autor:
Koichi Kusuhara, Toru Yoneda, Yasuhiko Takahashi, Takayuki Hoshina, Mayumi Kawase, Masumi Kojiro
Publikováno v:
Journal of Infection and Chemotherapy. 26:206-210
Rotavirus (RV) vaccine contributed to the reduction of the hospitalization for gastroenteritis (GE)-associated convulsion whereas there were few studies investigating the vaccination rate and the reduction of the disease simultaneously. The aim of th
Autor:
Ryoko Nakamura, Akira Mizushima, Wataru Shimabukuro, Mamie Watanabe, Yuichiro Sugitani, Yuka Sagara, Miwa Yoshino, Masahiko Joo, Yasuhiko Takahashi, Jun Muneuchi, Toru Yoneda
Publikováno v:
Pediatric Infectious Disease Journal. 38:e185-e187
We performed brain magnetic resonance imaging in 14 patients with Kawasaki disease who were treated with infliximab (IFX) at 56 months of age (32-62 months of age) and 23 months (5-35 months) after IFX therapy. Magnetic resonance imaging showed no fi
Autor:
Sumie Yamamoto, Yoshihiro Suzuki, Takushi Sato, Shuko Takahashi, Takashi Yorifuji, Hideki Hayashi, Hayato Orui, Hiroshi Sashiyama, Shigeru Suganami, Taro Hasegawa, Taro Sakai, Toru Yoneda, Maki Okamoto, Daisuke Kato, Yoshiomi Kishida
Publikováno v:
Archives of Environmental & Occupational Health. 73:284-291
Two huge earthquakes struck Kumamoto, Japan, in April 2016, forcing residents to evacuate. Few studies have reported early-phase disease and injury trends among evacuees following major inland earthquakes. We evaluated the trends among evacuees who v
Publikováno v:
No to hattatsu = Brain and development. 48(6)
Tuberous sclerosis complex (TSC) is a genetic disease affecting many organ systems and showing different symptoms in each age group. We encountered a TSC patient with intractable epilepsy who had brain tumors suspected to be subependymal giant cell a
Autor:
Tomokatsu Yoshida, Toru Yoneda, Takashi Shiihara, Masanori Nakagawa, Nobuzo Shimizu, Ikuko Mizuta
Publikováno v:
Brain and Development. 33:604-607
Alexander disease is a major entity of leukodystrophy; magnetic resonance imaging (MRI) studies of the brain typically show extensive changes in the cerebral white matter with frontal predominance. Heterozygous missense mutations of GFAP are thought