Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Masako Inaba"'
Autor:
Masatoshi Nakamura, Masashi Mizumoto, Takashi Saito, Shosei Shimizu, Yinuo Li, Yoshiko Oshiro, Masako Inaba, Sho Hosaka, Hiroko Fukushima, Ryoko Suzuki, Takashi Iizumi, Kei Nakai, Kazushi Maruo, Hideyuki Sakurai
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionChondrosarcoma is a rare malignant bone tumor. Particle beam therapy (PT) can concentrate doses to targets while reducing adverse events. A meta-analysis based on a literature review was performed to examine the efficacy of PT and photon
Externí odkaz:
https://doaj.org/article/df495b39bcd341b9913af835c6be226a
Autor:
Takashi Saito, Masashi Mizumoto, Yoshiko Oshiro, Shosei Shimizu, Yinuo Li, Masatoshi Nakamura, Sho Hosaka, Kei Nakai, Takashi Iizumi, Masako Inaba, Hiroko Fukushima, Ryoko Suzuki, Kazushi Maruo, Hideyuki Sakurai
Publikováno v:
Cancers, Vol 16, Iss 14, p 2569 (2024)
[Objective] The aim of this study was to compare the efficacy of particle beam therapy (PT) with photon radiotherapy (RT) for treatment of skull base chordoma. [Methods] A systematic review was conducted for skull base chordoma treated with PT or pho
Externí odkaz:
https://doaj.org/article/59b3593bad63425f8c163b0bbff841a1
Autor:
Moena Ishikawa, Yumi Tada, Hiromu Tanaka, Wataru Morii, Masako Inaba, Hidetoshi Takada, Takayasu Mori, Emiko Noguchi
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 10, Iss 2, Pp 71-78 (2020)
Gitelman syndrome (GS) is an autosomal recessive disorder characterized by alkalosis, hypokalemia, and hypomagnesemia. Although hundreds of genetic variants associated with GS have been reported, many of them are categorized as of uncertain significa
Externí odkaz:
https://doaj.org/article/d10e3bb601fd4cbcb524a7c61b66a087
Autor:
Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Sho Hosaka, Masako Inaba, Kouji Masumoto, Ai Muroi, Takao Tsurubuchi, Reiko Okubo, Kyoko Hidaka, Masashi Mizumoto, Hideyuki Sakurai, Hidetoshi Takada
Publikováno v:
International Journal of Clinical Oncology.
Autor:
Hiroko Fukushima, Masashi Mizumoto, Ryoko Suzuki, Yuni Yamaki, Sho Hosaka, Masako Inaba, Manabu Tagawa, Atsuko Watanabe, Tomoko Okunushi, Kouji Masumoto, Ai Muroi, Hideyuki Sakurai, Hidetoshi Takada
Publikováno v:
Japanese Journal of Clinical Oncology.
Background The details of gastrointestinal bleeding/ulcer in paediatric cancer patients treated with proton beam therapy have not been reported previously. Methods Patients aged 15 years or younger at the time of proton beam therapy and whose gastroi
Autor:
Morio Hasegawa, Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Sho Hosaka, Masako Inaba, Tomohei Nakao, Chie Kobayashi, Ai Yoshimi, Masahiro Tsuchida, Kazutoshi Koike, Takashi Fukushima, Hidetoshi Takada
Publikováno v:
Oncology. 100:376-383
Introduction: MEFV is the gene responsible for familial Mediterranean fever. It encodes pyrin, which controls inflammation. Besides, previous studies have reported that some germline MEFV variants were associated with tumour susceptibility. Materials
Autor:
Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Sho Hosaka, Masako Inaba, Ai Muroi, Takao Tsurubuchi, Wataru Morii, Emiko Noguchi, Hidetoshi Takada
Publikováno v:
Oncology. 100:163-172
Brain tumors affect one-third of all children with cancer. Approximately 10% of children with cancer carry variants in cancer-predisposition genes. However, germline analyses in large cohorts of Asian children have not been reported. Thirty-eight Jap
Autor:
Masako Inaba, Hiroko Fukushima, Monami Hara, Sho Hosaka, Satoshi Fujiyama, Kazushi Maruo, Toshifumi Nomura, Naoko Okiyama, Hidetoshi Takada
Publikováno v:
Clinical Immunology. 252:109649
Autor:
Takayasu Mori, Masako Inaba, Yumi Tada, Emiko Noguchi, Hidetoshi Takada, Wataru Morii, Moena Ishikawa, Hiromu Tanaka
Publikováno v:
Case Reports in Nephrology and Dialysis
Case Reports in Nephrology and Dialysis, Vol 10, Iss 2, Pp 71-78 (2020)
Case Reports in Nephrology and Dialysis, Vol 10, Iss 2, Pp 71-78 (2020)
Gitelman syndrome (GS) is an autosomal recessive disorder characterized by alkalosis, hypokalemia, and hypomagnesemia. Although hundreds of genetic variants associated with GS have been reported, many of them are categorized as of uncertain significa
Autor:
Zhijian Yao, Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Sho Hosaka, Masako Inaba, Satoshi Fujiyama, Hidetoshi Takada
Publikováno v:
Pediatrics International. 64
Childhood cancer survivors (CCSs) may have comorbidities including a long-term abnormality in the immune system. Immune reconstitution in CCSs after treatment for acute leukemia has been reported previously, while analyses of immune reconstitution in