Zobrazeno 1 - 10
of 90
pro vyhledávání: '"RIE IRIE"'
Autor:
Yohji Uehara, Yuka Sano Wada, Yuka Iwasaki, Kota Yoneda, Yasuhisa Ikuta, Shoichiro Amari, Hidehiko Maruyama, Keiko Tsukamoto, Tetsuya Isayama, Kenichi Sakamoto, Yoko Shioda, Osamu Miyazaki, Rie Irie, Takako Yoshioka, Naoko Mochimaru, Kazue Yoshida, Yushi Ito
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Systemic juvenile xanthogranuloma is a very rare disease typically presents as skin lesions with yellow papules or nodules and is sometimes fatal. We report a case of congenital neonatal systemic juvenile xanthogranuloma with atyp
Externí odkaz:
https://doaj.org/article/9f3e758b318c4b8a9add3412e2ee1ecd
Autor:
Toshiaki Teratani, Kengo Tomita, Hirotaka Furuhashi, Nao Sugihara, Masaaki Higashiyama, Makoto Nishikawa, Rie Irie, Takeshi Takajo, Akinori Wada, Kazuki Horiuchi, Kenichi Inaba, Yoshinori Hanawa, Naoki Shibuya, Yoshikiyo Okada, Chie Kurihara, Shin Nishii, Akinori Mizoguchi, Hideaki Hozumi, Chikako Watanabe, Shunsuke Komoto, Shigeaki Nagao, Junji Yamamoto, Soichiro Miura, Ryota Hokari, Tananori Kanai
Publikováno v:
Hepatology Communications, Vol 3, Iss 8, Pp 1098-1112 (2019)
Lipoprotein lipase (LPL) plays a central role in incorporating plasma lipids into tissues and regulates lipid metabolism and energy balance in the human body. Conversely, LPL expression is almost absent in normal adult livers. Therefore, its physiolo
Externí odkaz:
https://doaj.org/article/5122bbf478584d92b6b14cf523dfdf52
Autor:
Michinobu Ohno, Toshiko Takezoe, Toshihiko Watanabe, Kazunori Tahara, Tomoro Hishiki, Akihiro Fujino, Motomi Matsuo, Masataka Higuchi, Kazuteru Kawasaki, Yoko Shioda, Motohiro Kato, Chikako Kiyotani, Kimikazu Matsumoto, Emi Takakuwa, Rie Irie, Takako Yoshioka, Shunsuke Kimura, Masafumi Seki, Junko Takita, Yutaka Kanamori
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 19, Iss C, Pp 34-37 (2017)
Pleuropulmonary blastoma (PPB) is a rare malignant mesenchymal tumor. It is classified into 3 subgroups, and PPB type 1 is known to be a cystic lesion with good prognosis. Here, we report a case of PPB type 1 seen in a 1-year-old girl whose pulmonary
Externí odkaz:
https://doaj.org/article/bfa0e7e8512d4da4892e4872a96cd34d
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 2, Iss , Pp - (2015)
Incomplete abolition of tumorigenicity creates potential safety concerns in clinical trials of regenerative medicine based on human pluripotent stem cells (hPSCs). Here, we demonstrate that conditionally replicating adenoviruses that specifically tar
Externí odkaz:
https://doaj.org/article/10e0b06c99a74701bf2b53974620e3ae
Autor:
Takahiro Suyama, Masao Hagihara, Naruaki Matsui, Rie Irie, Yoshiyuki Osamura, Tetsuo Sakai, Shouichi Watanabe, Shintarou Umemoto, Naoki Miyao
Publikováno v:
Journal of Clinical and Experimental Hematopathology. 63:43-48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ae7e211664a0133f321d87bff47342
https://doi.org/10.3960/jslrt.22041
https://doi.org/10.3960/jslrt.22041
Autor:
Tomoo Osumi, Rie Irie, Mureo Kasahara, Atsuko Nakazawa, Yoko Shioda, Kenichi Sakamoto, Kimikazu Matsumoto
Publikováno v:
Journal of Clinical and Experimental Hematopathology. 62:25-34
Histiocytic neoplasms, such as Langerhans cell histiocytosis (LCH) and disseminated juvenile xanthogranuloma (JXG), can involve the liver and sometimes cause liver failure. We aimed to classify non-LCH histiocytic proliferating disorders that do not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c88fe15b1fe6b77998eae57064e3c222
https://doi.org/10.3960/jslrt.21022
https://doi.org/10.3960/jslrt.21022
Publikováno v:
Journal of Clinical and Experimental Hematopathology : JCEH
Tumor flare reaction (TFR) is a unique immune-mediated tumor recognition phenomenon presenting as rapid enlargement of the tumor, which mimics disease progression, developing in the early stage of treatment using immunomodulatory drugs or immune chec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43fcca9d10b4abfbc5bb98fa9d315f7
http://europepmc.org/articles/PMC8053573
http://europepmc.org/articles/PMC8053573
Autor:
Akinari Fukuda, Yusuke Yanagi, Atsuko Nakazawa, Rie Irie, Seisuke Sakamoto, Seiichi Shimizu, Reiko Horikawa, Mureo Kasahara, Hajime Uchida, Masahiro Takeda
Publikováno v:
Hepatology Research. 50:635-642
AIM It has been reported that the long-term outcome for children with metabolic disorders after liver transplantation (LT) is excellent. However, there are several reports citing LT patients with metabolic disorders developing liver dysfunction early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8635cce5c4ec5caa2a8e6bf707af5304
https://doi.org/10.1111/hepr.13487
https://doi.org/10.1111/hepr.13487
Publikováno v:
Cureus
Approximately 0.17-2% of mature cystic teratomas undergo malignant transformation, of which squamous cell carcinoma (SCC) is the most common, accounting for 80% of these cases. Urothelial malignant transformation is extremely rare. The present study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39832de66a7eb668e96377d1de72cb5d
http://europepmc.org/articles/PMC8450167
http://europepmc.org/articles/PMC8450167
Autor:
Takako Yoshioka, Yuka Iwasaki, Kazue Yoshida, Yasuhisa Ikuta, Shoichiro Amari, Yuka Sano Wada, Kenichi Sakamoto, Kota Yoneda, Yushi Ito, Keiko Tsukamoto, Yohji Uehara, Osamu Miyazaki, Naoko Mochimaru, Tetsuya Isayama, Rie Irie, Yoko Shioda, Hidehiko Maruyama
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
Background Systemic juvenile xanthogranuloma is a very rare disease typically presents as skin lesions with yellow papules or nodules and is sometimes fatal. We report a case of congenital neonatal systemic juvenile xanthogranuloma with atypical skin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad6588b3d00bb62d0deb64920bb920e
https://doi.org/10.1186/s12887-021-02632-0
https://doi.org/10.1186/s12887-021-02632-0