Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shizuka Kirino"'
Autor:
Shizuka Kirino, Hisae Nakatani, Aoi Honma, Asami Shinbo, Keiko Onda, Mari Okada, Masako Imai, Natsuko Suzuki, Akihiro Oshiba, Masayuki Nagasawa
Publikováno v:
Immunological Medicine, Vol 43, Iss 1, Pp 57-60 (2020)
An eight-year-old girl was admitted for prolonged fever and general fatigue. Bilateral reddened and swollen tonsils covered with white fur and increased numbers of atypical lymphocytes in blood led to a diagnosis of infectious mononucleosis (IM) due
Externí odkaz:
https://doaj.org/article/e70c9fbf79a14e0b90a566b6a87e1760
Autor:
Kei Takasawa, Ryosei Iemura, Ryuta Orimoto, Haruki Yamano, Shizuka Kirino, Eriko Adachi, Yoko Saito, Kurara Yamamoto, Nozomi Matsuda, Shigeru Takishima, Kumi Shuno, Hanako Tajima, Manabu Sugie, Yuki Mizuno, Akito Sutani, Kentaro Okamoto, Michiya Masue, Tomohiro Morio, Kenichi Kashimada
Publikováno v:
Clinical Pediatric Endocrinology; 2024, Vol. 33 Issue 3, p187-194, 8p
Autor:
Eriko Adachi, Ryuichi Nakagawa, Atsumi Tsuji-Hosokawa, Maki Gau, Shizuka Kirino, Analia Yogi, Hisae Nakatani, Kei Takasawa, Tomomi Yamaguchi, Tomoki Kosho, Masanori Murakami, Toshihiro Tajima, Tomonobu Hasegawa, Tetsuya Yamada, Tomohiro Morio, Osamu Ohara, Kenichi Kashimada
Publikováno v:
Journal of Clinical Endocrinology & Metabolism; Mar2024, Vol. 109 Issue 3, p750-760, 11p
Autor:
Shizuka Kirino, Analia Yogi, Eriko Adachi, Hisae Nakatani, Maki Gau, Ryosei Iemura, Haruki Yamano, Toru Kanamori, Takayasu Mori, Eisei Sohara, Shinichi Uchida, Kentaro Okamoto, Tomohiro Udagawa, Kei Takasawa, Tomohiro Morio, Kenichi Kashimada
Publikováno v:
Sexual Development.
Introduction: The variants in the zinc finger (ZF) domains 1–3 in WT1 are one of the major causes of 46,XY disorders of sex development. Recently, the variants in fourth ZF (ZF4 variants) were reported to cause 46,XX DSD. However, all the nine pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f628ba783d7666128fe853242888ffc0
https://doi.org/10.1159/000529720
https://doi.org/10.1159/000529720
Publikováno v:
Pediatrics International. 64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62b4a31e6dcffe104944eacd904fb0a1
https://doi.org/10.1111/ped.15157
https://doi.org/10.1111/ped.15157
Autor:
Shizuka Kirino, Mitsuyoshi Suzuki, Takuya Ogawa, Kei Takasawa, Eriko Adachi, Maki Gau, Ken Takahashi, Mitsuru Ikeno, Mamiko Yamada, Hisato Suzuki, Kenjiro Kosaki, Keiji Moriyama, Masayuki Yoshida, Tomohiro Morio, Kenichi Kashimada
Publikováno v:
European Journal of Medical Genetics. 65:104623
AMOTL1 is a member of the Motin protein family and localizes to tight junctions and is involved in cell polarity and paracellular permeability. Pathological variants have been reported in three patients from two separate families in recent years. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f057400ccc5882afa203ba5848885ef
https://doi.org/10.1016/j.ejmg.2022.104623
https://doi.org/10.1016/j.ejmg.2022.104623
Autor:
Tomohiro Morio, Takahiro Kamiya, Shizuka Kirino, Maki Gau, Akihiro Hoshino, Takeru Yamauchi, Hirokazu Kanegane, Kento Inoue, Kei Takasawa, Kenichi Kashimada
Publikováno v:
Pediatric Diabetes. 20:1035-1040
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked (IPEX) syndrome is an autoimmune disorder caused by the dysfunction of FOXP3, which leads to regulatory T-(Treg) cell dysfunction and subsequently autoimmunity including type 1 diabe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3db7151c204701c864b6250c076044df
https://doi.org/10.1111/pedi.12895
https://doi.org/10.1111/pedi.12895