Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Seishiro Nodomi"'
Autor:
Takayuki Hamabata, Katsutsugu Umeda, Kagehiro Kouzuki, Takayuki Tanaka, Tomoo Daifu, Seishiro Nodomi, Satoshi Saida, Itaru Kato, Shiro Baba, Hidefumi Hiramatsu, Mitsujiro Osawa, Akira Niwa, Megumu K. Saito, Yasuhiko Kamikubo, Souichi Adachi, Yoshiko Hashii, Akira Shimada, Hiroyoshi Watanabe, Kenji Osafune, Keisuke Okita, Tatsutoshi Nakahata, Kenichiro Watanabe, Junko Takita, Toshio Heike
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-4 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/b950f5eee1ed4eed9297ec002e679c2f
Publikováno v:
European Heart Journal - Case Reports. 7
Background Hypertensive crisis is a relatively rare condition among infants and usually occurs secondary to an underlying disease. If not managed promptly, it is life-threatening and can lead to irreversible damage to vital organs. While secondary hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f8198ca229907dd0d3e63b7f2f8302e
https://doi.org/10.1093/ehjcr/ytad131
https://doi.org/10.1093/ehjcr/ytad131
Autor:
Kosuke Tamefusa, Hisashi Ishida, Kiichiro Kanamitsu, Motoharu Ochi, Kaori Fujiwara, Yasuhisa Tatebe, Michinori Aoe, Seishiro Nodomi, Kana Washio
Publikováno v:
Pediatric Blood & Cancer. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e74f8fa3637a51e9e260df2274246a2
https://doi.org/10.1002/pbc.30108
https://doi.org/10.1002/pbc.30108
Autor:
Keiji Tasaka, Ken Morita, Katsutsugu Umeda, Seishiro Nodomi, Hidefumi Hiramatsu, Koji Kawaguchi, Tatsutoshi Nakahata, Kenichiro Watanabe, Hiroo Ueno, Toshio Heike, Satoshi Saida, Hajime Hosoi, Shigeki Yagyu, Hideto Ogata, Junko Takita, Kagehiro Kouzuki, Eri Ogawa, Hideaki Okajima, Souichi Adachi, Tatsuya Okamoto, Mari Sonoda, Yasuhiko Kamikubo, Hideto Iwafuchi, Itaru Kato, Satoshi Obu, Shinji Uemoto, Tomoko Iehara
Publikováno v:
Cancer Science
Neuroblastoma, the most common extracranial solid tumor of childhood, is thought to arise from neural crest‐derived immature cells. The prognosis of patients with high‐risk or recurrent/refractory neuroblastoma remains quite poor despite intensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42e3382ba2480ae921bc34ccffa88218
https://doi.org/10.1111/cas.15124
https://doi.org/10.1111/cas.15124
Autor:
Itaru Kato, Akira Shimada, Katsutsugu Umeda, Yasuhiko Kamikubo, Tomoo Daifu, Shiro Baba, Hidefumi Hiramatsu, Mitsujiro Osawa, Seishiro Nodomi, Kenichiro Watanabe, Yoshiko Hashii, Tatsutoshi Nakahata, Keisuke Okita, Souichi Adachi, Junko Takita, Takayuki Tanaka, Kenji Osafune, Toshio Heike, Megumu K. Saito, Akira Niwa, Hiroyoshi Watanabe, Takayuki Hamabata, Satoshi Saida, Kagehiro Kouzuki
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-4 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0dbea8de07da3f3f58b4da9063b5f02
https://doi.org/10.1038/s41598-021-81066-1
https://doi.org/10.1038/s41598-021-81066-1
Autor:
Akira Niwa, Junko Takita, Akira Shimada, Yasuhiko Kamikubo, Itaru Kato, Kenichiro Watanabe, Yoshiko Hashii, Tomoo Daifu, Shiro Baba, Tatsutoshi Nakahata, Takayuki Hamabata, Takayuki Tanaka, Satoshi Saida, Mitsujiro Osawa, Seishiro Nodomi, Hiroyoshi Watanabe, Toshio Heike, Keisuke Okita, Kenji Osafune, Megumu K. Saito, Kagehiro Kouzuki, Katsutsugu Umeda, Hidefumi Hiramatsu, Souichi Adachi
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Shwachman–Diamond syndrome (SDS), an autosomal recessive disorder characterized by bone marrow failure, exocrine pancreatic insufficiency, and skeletal abnormalities, is caused by mutations in the Shwachman–Bodian–Diamond syndrome (SBDS) gene,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5899be625cd4f02cae6cadd65b6ae18
https://doi.org/10.1038/s41598-020-71844-8
https://doi.org/10.1038/s41598-020-71844-8
Autor:
Seishiro Nodomi, Takashi Mizowaki, Toshio Heike, Hiroo Ueno, Yoshiki Arakawa, Takeshi Funaki, Satoshi Saida, Katsutsugu Umeda, Hidefumi Hiramatsu, Souichi Adachi
Publikováno v:
Journal of Pediatric Hematology/Oncology. 39:e39-e42
Intracranial germ cell tumor is sometimes associated with Down syndrome; however, no optimal treatment has been developed due to the high risk of recurrence and treatment-related mortality. Here, we report on a patient with an intracranial germinoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26cf7d47db2e0c520c2864e30d04aaa3
https://doi.org/10.1097/mph.0000000000000711
https://doi.org/10.1097/mph.0000000000000711
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 59(11)
A 13-year-old female developed L-asparaginase (L-ASP) -associated thrombosed external hemorrhoids (TEH) during chemotherapy for Philadelphia chromosome-positive acute lymphoblastic leukemia. While undergoing induction therapy combined with imatinib,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a437094eb0b7020e7a445abe75aef12a
https://pubmed.ncbi.nlm.nih.gov/30531135
https://pubmed.ncbi.nlm.nih.gov/30531135
Autor:
Satoshi Obu, Katsutsugu Umeda, Hiroo Ueno, Mari Sonoda, Keiji Tasaka, Hideto Ogata, Kagehiro Kouzuki, Seishiro Nodomi, Satoshi Saida, Itaru Kato, Hidefumi Hiramatsu, Tatsuya Okamoto, Eri Ogawa, Hideaki Okajima, Ken Morita, Yasuhiko Kamikubo, Koji Kawaguchi, Kenichiro Watanabe, Hideto Iwafuchi, Shigeki Yagyu
Publikováno v:
Cancer Science; Nov2021, Vol. 112 Issue 11, p4617-4626, 10p
Autor:
Seishiro Nodomi, Katsutsugu Umeda, Hidefumi Hiramatsu, Tomoko Iehara, Kinehara T, Tomoo Daifu, Toshio Heike, Yasumichi Kuwahara, Eiichi Konishi, Souchi Adachi, Satoshi Saida, Kenichiro Watanabe, Takayuki Hamabata, Tatsutoshi Nakahata, Itaru Kato, Hajime Hosoi
Publikováno v:
Oncogene
Malignant rhabdoid tumor (MRT) is a rare, highly aggressive pediatric malignancy that primarily develops during infancy and early childhood. Despite the existing standard of intensive multimodal therapy, the prognosis of patients with MRT is dismal;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e668841f0cff1ca61eba21d555a8a2b
https://doi.org/10.1038/onc.2016.72
https://doi.org/10.1038/onc.2016.72