Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Genrei Ohta"'
Autor:
Toshihide Yoshikawa, Akihiko Tanizawa, Koji Suzuki, Nanae Tanaka, Taihei Hayashi, Masayo Tsuda, Genrei Ohta, Naoko Kikuchi, Hiroyuki Okamoto, Takehiko Sakai, Yoshihiro Taniguchi, Yusei Ohshima
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
The patients with acute leukemia occasionally present with musculoskeletal symptoms initially, including bone pain, joint pain, muscular pain, and functional impairment. Without abnormal findings of peripheral blood cell counts or smear, the correct
Externí odkaz:
https://doaj.org/article/515ea1b68d84452db76087bdcdf2854b
Publikováno v:
Pediatrics International. 63:561-564
Background Our peripherally inserted central venous catheter (PICC) management plan for neonates previously included routine inspection for swelling and induration of the insertion site of a PICC using palpation. However, we discontinued routine palp
Autor:
Mari Asaoka, Tetsuhiro Fukuyama, Naohisa Kawamura, Tamami Yano, Takayoshi Kawabata, Kotaro Nakano, Eriko Kikuchi, Tomoyuki Miyamoto, Mika Inoue, Akihisa Okumura, Masato Hiyane, Etsushi Toyofuku, Yuichi Takami, Yusaku Endo, Keiko Tanaka-Taya, Nobuyoshi Sugiyama, Yu Tsuyusaki, Sawa Yasumoto, Keiko Suzuki, Nobuko Moriyama, Takako Fujita, Yasuhiro Suzuki, Eri Takeshita, Hitoshi Mikami, Yuichi Abe, Ryutaro Kira, Chiharu Miyatake, Hiroyuki Torisu, Akira Kumakura, Akane Kanazawa, Tatsuharu Sato, Yuya Takahashi, Hiroshi Terashima, Sonoko Kubota, Genrei Ohta, Mariko Kasai, Yu Ishida, Pin Fee Chong, Noboru Yoshida, Shinichiro Goto, Taira Toki, Ayako Hattori, Wakako Ishii, Kenichi Tanaka, Miho Yamamuro, Sahoko Ono, Yukihiko Konishi, Harushi Mori, Nozomi Koran, Kazuhide Ohta, Kenichi Sakajiri, Michiaki Nagura, Kyoko Ban
Publikováno v:
Pediatric Neurology. 116:14-19
We summarize the long-term motor outcome and disability level in a cluster of pediatric patients with acute flaccid myelitis (AFM) associated with the enterovirus D68 outbreak in 2015.This is a nationwide follow-up questionnaire analysis study. Clini
Publikováno v:
Brain and Development. 41:717-720
Background Early myoclonic encephalopathy (EME) is an epileptic syndrome that develops in neonates, commonly within 1 month of birth. The condition is characterized by irregular, partial, and asynchronous myoclonus. The seizures in EME are generally
Autor:
Genrei Ohta, Shinichiro Takiguchi, Hisako Hayashi, Takashi X. Fujisawa, Takuya Kosaka, Akio Fujine, Yusei Ohshima, Akemi Tomoda, Yoshifumi Mizuno, Akemi Tsuda, Masao Kawatani, Asami Kumano
Publikováno v:
Braindevelopment. 43(1)
Aims The current study aimed to validate the relationship between sensory characteristics and sleep dynamics among children with autism spectrum disorder (ASD) using an actigraph, which is an objective assessment device used for sleep monitoring. Met
Autor:
Ai Takahashi, Seiichiro Shimada, Genrei Ohta, Erina Kamei, Yuri Sato, Akihiko Matsumine, Yusei Ohshima, Misao Tsubokawa
Publikováno v:
Medicine
Rationale: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a condition characterized by biphasic convulsions and disturbance of consciousness. In Japan, the most common pediatric cases of acute encephalopathy are asso
Autor:
Nanae Tanaka, Taihei Hayashi, Yoshihiro Taniguchi, Takehiko Sakai, Toshihide Yoshikawa, Yusei Ohshima, Naoko Kikuchi, Koji Suzuki, Masayo Tsuda, Hiroyuki Okamoto, Akihiko Tanizawa, Genrei Ohta
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
Case Reports in Pediatrics
Case Reports in Pediatrics
The patients with acute leukemia occasionally present with musculoskeletal symptoms initially, including bone pain, joint pain, muscular pain, and functional impairment. Without abnormal findings of peripheral blood cell counts or smear, the correct
Publikováno v:
Lung
Purpose Bronchopulmonary dysplasia (BPD) is a respiratory complication characterized by abnormal alveolar development in premature infants. Geranylgeranylacetone (GGA) can induce heat shock protein (HSP) 70, which has cytoprotective effects against v
Publikováno v:
Disease Markers, Vol 2017 (2017)
Disease Markers
Disease Markers
Background. Refeeding syndrome is characterized by metabolic disturbance including hypophosphatemia and hypokalemia upon reinstitution of nutrition in severely malnourished patients. Objective. The present study sought to identify the risk factors fo
Publikováno v:
Pediatric nephrology (Berlin, Germany). 32(10)
The number of nephrons at birth is determined during fetal development and is modulated thereafter by postnatal podocyte injury. Hyperfiltration, caused by a reduced number of nephrons, is a risk factor for chronic kidney disease. It is therefore imp