Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Takayo Urata"'
Autor:
Kenji Okamoto, Toshihiko Imamura, Seiji Tanaka, Takayo Urata, Hideki Yoshida, Norio Shiba, Tomoko Iehara
Publikováno v:
International Journal of Hematology.
Autor:
Hiroaki Kondo, Takuyo Kanayama, Utsuki Matsumura, Takayo Urata, Shinya Osone, Toshihiko Imamura, Tohru Inaba, Hajime Hosoi
A 7-year-old boy was diagnosed with RUNX1-RUNX1T1-positive acute myeloid leukemia. Although he achieved complete remission (CR) after conventional chemotherapy, he experienced relapse 6 months after completing initial treatment. The cytoplasm of myel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::022aafb45d1b271dd89d02ec9967082d
https://doi.org/10.22541/au.164864218.86270091/v1
https://doi.org/10.22541/au.164864218.86270091/v1
Autor:
Hajime Hosoi, Hideki Muramatsu, Toshihiko Imamura, Shinya Osone, Takayo Urata, Yoshiyuki Takahashi
Publikováno v:
Journal of pediatric hematology/oncology. 44(2)
Fanconi anemia (FA) is a rare genetic disorder that manifests as congenital abnormalities and bone marrow failure (BMF). Most patients with FA present with BMF within the first decade of life; however, neonate and early infancy BMF is rare. Recent st
Autor:
Takayo Urata, Utsuki Matsumura, Hiroaki Kondo, Tohru Inaba, Takuyo Kanayama, Shinya Osone, Hajime Hosoi, Toshihiko Imamura
Publikováno v:
International Journal of Hematology. 113:616-617
Autor:
Shinichi Tamura, Hajime Hosoi, Junko Do, Hiroyuki Ishida, Hiroshi Kuroda, Mari Gen, Miki Kobayashi, Toshihiko Imamura, Takayo Urata, Shinya Osone, Toshihiro Tomii
Publikováno v:
Journal of Pediatric Hematology/Oncology. 39:e394-e398
Although bone marrow failure in patients with dyskeratosis congenita (DKC) can be successfully treated with allogeneic hematopoietic cell transplantation (allo-HCT) using a reduced intensity conditioning (RIC) regimen, the outcome of nonhematological