Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Chie, Kobayashi"'
Autor:
Etsushi Toyofuku, Kozue Takeshita, Hidenori Ohnishi, Yuko Kiridoshi, Hiroaki Masuoka, Tomonori Kadowaki, Ryuta Nishikomori, Kenichi Nishimura, Chie Kobayashi, Takasuke Ebato, Tomonari Shigemura, Yuzaburo Inoue, Wataru Suda, Masahira Hattori, Tomohiro Morio, Kenya Honda, Hirokazu Kanegane
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 11 (2022)
IntroductionHaploinsufficiency of A20 (HA20) is a form of inborn errors of immunity (IEI). IEIs are genetically occurring diseases, some of which cause intestinal dysbiosis. Due to the dysregulation of regulatory T cells (Tregs) observed in patients
Externí odkaz:
https://doaj.org/article/7def3c4cc537413ba58d2b7e13017a76
Autor:
Kunio Fukuda, Ai Yoshimi, Miki Toma, Satoru Matsushima, Norihiko Kitagawa, Masato Shinkai, Noritaka Ota, Toshihide Asou, Mio Tanaka, Yukichi Tanaka, Chie Kobayashi, Takayuki Masuko, Asai Nobuyoshi, Keisuke Kato, Junko Shiono, Haruo Ohtani, Kazutoshi Koike, Tatsuo Kono, Toshihiro Yanai, Masahiro Tsuchida
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 66, Iss , Pp 101705- (2021)
Undifferentiated embryonal sarcoma of the liver (UESL) is a highly malignant neoplasm occurring predominantly in children. Complete resection is the only curative treatment. We encountered an 11-year-old boy with UESL arising in the right lobe of the
Externí odkaz:
https://doaj.org/article/e8a6d906df0c4e0f8119209e131a5c24
Autor:
Rie Iizuka, Chie Kobayashi
Publikováno v:
Philosophical Psychology. 36:834-845
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1855820dff5dfe81c93f8e01ccbc444
https://doi.org/10.1080/09515089.2023.2191635
https://doi.org/10.1080/09515089.2023.2191635
Autor:
Masanobu Miura, Satoru Miyaishi, Kaori Taniguchi, Yukie Yamasaki, Chie Kobayashi, Sella Takei, Yasuhiro Aoki
Publikováno v:
Okayama Igakkai Zasshi (Journal of Okayama Medical Association). 134:108-114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60307ff2ad5a4d2aff29cdd34a6bddc8
https://doi.org/10.4044/joma.134.108
https://doi.org/10.4044/joma.134.108
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::065b0848295f05533986615b54d82e69
https://doi.org/10.7759/cureus.34627
https://doi.org/10.7759/cureus.34627
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f450ae045553ca34b8f2e0062ca75512
https://doi.org/10.1159/000524833
https://doi.org/10.1159/000524833
Autor:
Dan Tomomasa, Claire Booth, Jack J. Bleesing, Takeshi Isoda, Chie Kobayashi, Kazutoshi Koike, Takeshi Taketani, Akihisa Sawada, Akihiro Tamura, Rebecca A. Marsh, Tomohiro Morio, Andrew R. Gennery, Hirokazu Kanegane
Publikováno v:
Clinical immunology (Orlando, Fla.). 237
Few reports have examined whether prophylactic allogeneic hematopoietic cell transplantation (HCT) for X-linked lymphoproliferative syndrome type 1 (XLP1) improves the prognosis. We compared the prognosis of symptomatic probands and affected siblings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e0d3713b5537abb01f7798be7d1bf2
https://pubmed.ncbi.nlm.nih.gov/35367395
https://pubmed.ncbi.nlm.nih.gov/35367395
Autor:
Shinji Tanigaki, Aya Kitamura, Hiroshi Yoshihashi, Kana Tsushima, Chie Kobayashi, China Nagano, Yoichi Kobayashi, Atsushi Tajima, Miho Matsuhima, Kyoko Sakaguchi, Kandai Nozu, Yutaro Uchiumi, Satoshi Takemori
Publikováno v:
European journal of medical genetics. 64(10)
Transient antenatal Bartter syndrome due to melanoma-associated antigen D2 gene mutation is a newly reported type of Bartter syndrome. Its characteristics include an X-linked inheritance pattern, early-onset hydramnios, and spontaneous disappearance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25f265b818473551cffd26a41ef04f4b
https://pubmed.ncbi.nlm.nih.gov/34400373
https://pubmed.ncbi.nlm.nih.gov/34400373
Publikováno v:
Pediatrics International. 63:973-974
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb73f87c12cd75b02f91fec9f41b286
https://doi.org/10.1111/ped.14510
https://doi.org/10.1111/ped.14510
Autor:
Takahiro Kido, Chie Kobayashi, Tatsuyuki Ohto, Yukitoshi Takahashi, Ryo Sumazaki, Takashi Fukushima
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 9, Pp 5687-5691 (2017)
Background Anti-N-methyl- d-aspartate receptor (anti-NMDAR) encephalitis is an autoimmune neurological disorder that usually occurs as a paraneoplastic syndrome and is particularly associated with ovarian teratoma. Standard therapy for severe cases i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::6094d658ecf2a19d41a532468b5662f4
http://ijp.mums.ac.ir/article_9035_7aa549f5464d9b88989df47eac6e9bf5.pdf
http://ijp.mums.ac.ir/article_9035_7aa549f5464d9b88989df47eac6e9bf5.pdf