Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hitomi Niijima"'
Autor:
Takahiro Ikeda, Yuta Kawahara, Akihiko Miyauchi, Hitomi Niijima, Rieko Furukawa, Nobuyuki Shimozawa, Akira Morimoto, Hitoshi Osaka, Takanori Yamagata
Publikováno v:
JIMD Reports, Vol 63, Iss 1, Pp 19-24 (2022)
Abstract Adrenoleukodystrophy (ALD) is a peroxisomal disorder characterized by white matter degeneration caused by adenosine triphosphate‐binding cassette subfamily D member 1 (ABCD1) gene mutations, which lead to an accumulation of very‐long‐c
Externí odkaz:
https://doaj.org/article/780fcfc1716c48bbad54e7aacb6a724f
Autor:
Taiju Hyuga, Shigeru Nakamura, Kazuya Tanabe, Taro Kubo, Hitomi Niijima, Yuta Kawahara, Waka Nakata, Rieko Furukawa, Mio Sakaguchi, Akira Shimada, Mitsuru Matsuki, Toshiro Niki, Yasunori Kamiyama, Kimihiko Moriya, Hideo Nakai
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 86, Iss , Pp 102472- (2022)
We report a case of a girl with inverted papilloma of the urinary bladder, which was detected by ultrasonographic screening based on the findings of a school medical checkup. The case was an 11-year-old girl. She was diagnosed as having occult hematu
Externí odkaz:
https://doaj.org/article/c0144c0cb8af4557867dc3305cca4d7e
Publikováno v:
Journal of Pediatric Hematology/Oncology; Jan2024, Vol. 46 Issue 1, pe103-e106, 4p
Autor:
Takahiro Ikeda, Hitomi Niijima, Hitoshi Osaka, Akihiko Miyauchi, Rieko Furukawa, Nobuyuki Shimozawa, Yuta Kawahara, Akira Morimoto, Takanori Yamagata
Publikováno v:
JIMD Reports
JIMD Reports, Vol 63, Iss 1, Pp 19-24 (2022)
JIMD Reports, Vol 63, Iss 1, Pp 19-24 (2022)
Adrenoleukodystrophy (ALD) is a peroxisomal disorder characterized by white matter degeneration caused by adenosine triphosphate‐binding cassette subfamily D member 1 (ABCD1) gene mutations, which lead to an accumulation of very‐long‐chain fatt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73c714c382592bdaac7d479a64966688
http://europepmc.org/articles/PMC8743339
http://europepmc.org/articles/PMC8743339
Autor:
Akira Tanaka, Yoshikazu Yasuda, Yasunaru Sakuma, Yuta Kawahara, Koichi Mizuta, Shinya Otomo, Alan Kawarai Lefor, Noriki Okada, Taizen Urahashi, Akira Morimoto, Hitomi Niijima, Yukihiro Sanada, Naohiro Sata, Yuta Hirata
Publikováno v:
American Journal of Transplantation. 21:3184-3189
Maternal T cells from perinatal transplacental passage have been identified in up to 40% of patients with severe combined immunodeficiency (SCID). Although engrafted maternal T cells sometimes injure newborn tissue, liver failure due to maternal T ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec878bc3ebc1743623319d9523849474
https://doi.org/10.1111/ajt.16588
https://doi.org/10.1111/ajt.16588
Autor:
Akira Morimoto, Yasunaru Sakuma, Hitomi Niijima, Yukiko Oh, Yukihiro Sanada, Yuta Kawahara, Noriki Okada, Yasuharu Onishi, Hiroki Yoshinari, Yuta Hirata
Publikováno v:
International journal of hematology. 114(4)
Patients with hepatitis-associated aplastic anemia (HAA) who undergo living-donor liver transplantation (LDLT) have a poor prognosis with infections and bleeding complications. Rapid recovery of blood cells is critical for preventing these complicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4326d1b8454b4a8a059e0ce10a251304
https://pubmed.ncbi.nlm.nih.gov/34110619
https://pubmed.ncbi.nlm.nih.gov/34110619
Autor:
Tatsuhiro Ishida, Yuta Kawahara, Tomomi Hayase, Yukiko Oh, Hitomi Niijima, Taro Shimizu, Akira Morimoto
Publikováno v:
Haemophilia. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cee90e267800362e30136b34e41f314
https://doi.org/10.1111/hae.14048
https://doi.org/10.1111/hae.14048
Autor:
Shinsaku Imashuku, Kenichiro Watanabe, Tomomi Hayase, Takako Yoshioka, Yoko Shioda, Hitomi Niijima, Shiori Saito, Kentaro Ohki, Yukiko Oh, Yuta Kawahara, Toshihiko Imamura, Akira Morimoto
Publikováno v:
International journal of hematology. 112(4)
In Langerhans cell histiocytosis (LCH), somatic gene mutations in the mitogen-activated protein kinase pathway have been identified in more than 80% of cases in Western countries, in which mutually exclusive BRAF and MAP2K1 mutations are involved. Am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21510a772f1f35c285e1cd6300aa43c8
https://pubmed.ncbi.nlm.nih.gov/32654047
https://pubmed.ncbi.nlm.nih.gov/32654047
Autor:
Tomomi, Hayase, Hitomi, Niijima, Daisuke, Tanaka, Syoya, Wada, Yuta, Kawahara, Yukiko, Oh, Akira, Morimoto
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 57(7)
Pediatric anaplastic large cell lymphoma (ALCL) is a chemosensitive malignancy, but about 30% of patients experience relapse. In most of these patients, a second complete remission is obtainable with salvage chemotherapy, though relapse free survival
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::021f28c5e37a373eaa90065b6202b5eb
https://pubmed.ncbi.nlm.nih.gov/27498729
https://pubmed.ncbi.nlm.nih.gov/27498729