Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chikako Kamae"'
Autor:
China Nagano, Taishi Nada, Ryutaro Suzuki, Toru Kanamori, Koichi Nakanishi, Mai Sato, Kentaro Nishi, Masao Ogura, Chikako Kamae, Kandai Nozu, Kazumoto Iijima, Koichi Kamei, Miki Murakoshi
Publikováno v:
Clinical and Experimental Nephrology. 26:162-169
The management of congenital nephrotic syndrome of the Finnish type (CNF) is challenging. It is difficult to withdraw intravenous albumin infusions, resulting in long-term hospitalization. In addition, fatal hypotension after bilateral nephrectomy ha
Autor:
Chikako Kamae, Kentaro Nishi, Masao Ogura, Mai Sato, Ryutaro Suzuki, Toru Kanamori, Koichi Kamei, Miki Murakoshi
Publikováno v:
Japanese journal of pediatric nephrology. 33:23-28
Autor:
Kazuo Imai, Fumika Tanaka, Shuichi Kawano, Kotoba Esaki, Junko Arakawa, Takashi Nishiyama, Soichiro Seno, Kosuke Hatanaka, Takao Sugiura, Yu Kodama, Seigo Yamada, Shinichiro Iwamoto, Shigeto Takesima, Nobujiro Abe, Chikako Kamae, Shigeaki Aono, Toshimitsu Ito, Tetsuo Yamamoto, Yasunori Mizuguchi
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 10:2667-2676.e10
BackgroundWith the implementation of mass vaccination campaigns against COVID-19, the safety of vaccine needs to be evaluated.ObjectiveWe aimed to assess the incidence and risk factors for immediate hypersensitivity reactions (IHSR) and immunisation
Autor:
Miki, Murakoshi, Koichi, Kamei, Masao, Ogura, Mai, Sato, Taishi, Nada, Ryutaro, Suzuki, Chikako, Kamae, Kentaro, Nishi, Toru, Kanamori, China, Nagano, Kandai, Nozu, Koichi, Nakanishi, Kazumoto, Iijima
Publikováno v:
Clinical and experimental nephrology. 26(2)
The management of congenital nephrotic syndrome of the Finnish type (CNF) is challenging. It is difficult to withdraw intravenous albumin infusions, resulting in long-term hospitalization. In addition, fatal hypotension after bilateral nephrectomy ha
Autor:
Tomohiro Morio, Tsubasa Okano, Yujin Sekinaka, Eri Endo, Katsuyuki Hanabusa, Ikuya Tsuge, Shiann Tarng Jou, Masataka Ishimura, Hsin-Hui Yu, Yoshihiro Maruo, Tomiko Kimoto, Tomoaki Kunitsu, Hiroshi Yagasaki, Masami Inoue, Kenichi Yoshida, Yuki Tsujita, Taizo Wada, Kohsuke Imai, Kyoko Suzuki, Seiji Kojima, Sven Kracker, Tetsuzo Tauchi, Yuko Hashimoto, Takehiro Takashima, Yuzaburo Inoue, Toru Uchiyama, Hidetoshi Takada, Kenichi Honma, Motohiro Kato, Masakazu Nagahori, Takashi Kaneko, Yoshiaki Shikama, Naohiko Moriguchi, Tomoko Waragai, Daiei Kojima, Haruka Hiroki, Tamaki Kato, Kanako Mitsui-Sekinaka, Keisuke Tanaka, Anne Durandy, Yuki Bando, Hideki Muramatsu, Kazuhiro Tasaki, Seishi Ogawa, Hirokazu Kanegane, Fuminori Iwasaki, Shigeaki Nonoyama, Tzu Wen Yeh, Chikako Kamae, Toshihiko Shirakawa, Osamu Suzuki, Tomoyo Matsubara, Hideki Sano, Yuki Yuza, Osamu Ohara, Noriko Mitsuiki
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:266-275
Background Activated phosphatidylinositol-3-OH kinase δ syndrome type 1 (APDS1) is a recently described primary immunodeficiency syndrome characterized by recurrent respiratory tract infections, lymphoid hyperplasia, and Herpesviridae infections cau
Autor:
Masao Ogura, Ryutaro Suzuki, Mai Sato, Koichi Kamei, Kentaro Nishi, Chikako Kamae, Toru Kanamori, Miki Murakoshi
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(6)
Eosinophilic peritonitis (EP) is sometimes difficult to distinguish from bacterial peritonitis (BP) at onset, as they are often overlapping. Previous reports show EP occurs more frequently in infants, although the reason is unknown. The study populat
Autor:
Akira Ohara, Tomohiro Morio, Hirokazu Kanegane, Kenichi Honma, Tomonari Shigemura, Shigeaki Nonoyama, Chikako Kamae, Emiko Noguchi, Hiroyuki Sasaki, Tzu Wen Yeh, Shunichi Takakura, Aoi Honma, Tamaki Kato, Tomoko Shigemori, Kohsuke Imai, Masatoshi Hayashi, Osamu Ohara, Tsubasa Okano, Noriko Nakagawa, Watanabe Seiichi, Hiroshi Takahashi, Takeo Kubota
Publikováno v:
Journal of Clinical Immunology. 38:927-937
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare autosomal recessive primary immunodeficiency. Hypogammaglobulinemia is a major manifestation of ICF syndrome, but immunoglobulin replacement therapy does not see
Autor:
Kohsuke Imai, Chikako Kamae, Yuki Tsujita, Shigeaki Nonoyama, Kenichi Honma, Takahiko Horiuchi
Publikováno v:
Journal of Clinical Immunology. 38:144-148
A 42-year-old man with hyper-IgM syndrome type 2 caused by activation-induced cytidine deaminase (AID) deficiency developed a severe anaphylactic reaction to intravenous immunoglobulin. The purpose of this study was to clarify the cause of the anaphy
Autor:
Noriko Nakagawa, Kenichi Honma, Deepti Suri, Koon-Wing Chan, Yu-Lung Lau, Shigeaki Nonoyama, Osamu Ohara, Anju Gupta, Biman Saikia, Amit Rawat, Ravinder Garg, Kohsuke Imai, Surjit Singh, Chikako Kamae, Koichi Oshima, Ranjana W. Minz, Noriko Mitsuiki, Shobha Sehgal
Publikováno v:
Annals of Allergy, Asthma & Immunology. 117:405-411
Background X-linked agammaglobulinemia (XLA) is an X-linked genetic defect in maturation of B lymphocytes that results in the absence of B lymphocytes in the peripheral blood and profound hypogammaglobulinemia. It is caused by a mutation in the BTK g
Autor:
Tomoko Yokosuka, Shigeaki Nonoyama, Elena Crestani, Akihiro Yachie, Taizo Wada, Chikako Kamae, Takeshi Ikegawa, Hirokazu Kanegane, Tamaki Kato, Kenichi Honma, Kohsuke Imai, Luigi D. Notarangelo, Osamu Ohara, Tomohiro Morio, Naonori Nishida
Publikováno v:
Journal of Clinical Immunology. 35:280-288
Recombination-activating gene (RAG) 1 and 2 deficiency is seen in patients with severe combined immunodeficiency (SCID) and Omenn syndrome. However, the spectrum of the disease has recently expanded to include a milder phenotype.We analyzed a 4-year-