Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Tomohiro, Hirade"'
Autor:
Tomohiro Hirade, Ai Harada, Daisuke Koike, Yasuhiro Abe, Tsuyoshi Higuchi, Fumihide Kato, Bin Chang, Akiyoshi Nariai
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Invasive pneumococcal disease (IPD) is defined by the detection of Streptococcus pneumoniae on culture from samples obtained from a normally sterile site. Pneumococcal conjugate vaccines (PCV) have been developed for the preventio
Externí odkaz:
https://doaj.org/article/409249c589234cabbf4ea58b78cae304
Autor:
Tomohiro Hirade, Yasuhiro Abe, Satoko Ito, Tadaki Suzuki, Harutaka Katano, Naoto Takahashi, Daisuke Koike, Akiyoshi Nariai, Fumihide Kato
Publikováno v:
Pediatric Infectious Disease Journal; Nov2023, Vol. 42 Issue 11, p1002-1006, 5p
Autor:
Seiji, Fukuda, Nozomi, Matsuda, Tsukimi, Shoji, Chie, Onishi, Tomohiro, Hirade, Takeshi, Taketani, Louis M, Pelus
Publikováno v:
Leukemia research. 124
CXCR4 antagonists sensitize FLT3/ITD
Publikováno v:
Pediatrics International. 64
Publikováno v:
Pediatrics International. 64
Autor:
Mariko Abe, Louis M Pelus, Pratibha Singh, Tomohiro Hirade, Chie Onishi, Jamiyan Purevsuren, Takeshi Taketani, Seiji Yamaguchi, Seiji Fukuda
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0158290 (2016)
Internal tandem duplication (ITD) mutations in the Fms-related tyrosine kinase 3 (FLT3) gene (FLT3-ITD) are associated with poor prognosis in patients with acute myeloid leukemia (AML). Due to the development of drug resistance, few FLT3-ITD inhibito
Externí odkaz:
https://doaj.org/article/40eda58f1ea4428796a81aa963d31a58
Publikováno v:
International journal of pediatricsadolescent medicine. 9(3)
Laryngeal web is a rare congenital or acquired disease that results in airway stenosis. Depending on the severity of atresia, patients with laryngeal web show a wide variety of symptoms ranging from asymptomatic to life-threatening respiratory dysfun
Autor:
Seiji Fukuda, Nozomi Matsuda, Tsukimi Shoji, Chie Onishi, Tomohiro Hirade, Takeshi Taketani, Louis M. Pelus
Publikováno v:
Leukemia Research. 124:106983
Autor:
Takeshi Taketani M.D., Ph.D., Chigusa Oyama, Aya Mihara, Yuka Tanabe, Mariko Abe, Tomohiro Hirade, Satoshi Yamamoto, Ryosuke Bo, Rie Kanai, Taku Tadenuma, Yuko Michibata, Soichiro Yamamoto, Miho Hattori, Yoshihiro Katsube, Hiroe Ohnishi, Mari Sasao, Yasuaki Oda, Koji Hattori, Shunsuke Yuba, Hajime Ohgushi, Seiji Yamaguchi
Publikováno v:
Cell Transplantation, Vol 24 (2015)
Patients with severe hypophosphatasia (HPP) develop osteogenic impairment with extremely low alkaline phosphatase (ALP) activity, resulting in a fatal course during infancy. Mesenchymal stem cells (MSCs) differentiate into various mesenchymal lineage
Externí odkaz:
https://doaj.org/article/ba2f5b1d1dc14e879864c13230233920
Autor:
Yasuhiro Abe, Daisuke Koike, Akiyoshi Nariai, Akiyoshi Horie, Tomohiro Hirade, Tomoko Ito, Fumihide Katou
Publikováno v:
Pediatrics International
Background The hypothesis of the Developmental Origins of Health and Disease states that environmental factors during fetal and infantile life are risk factors for some chronic diseases in adulthood. Few studies, however, have confirmed this hypothes