Výsledky vyhledávání - Tanaka, Ryojiro
- Zobrazuji výsledky 1 - 13 z 13
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Candidate gene analysis using genomic quantitative PCR: identification of ADAMTS13 large deletions in two patients with Upshaw-Schulman syndrome Autor Eura, Yuka, Kokame, Koichi, Takafuta, Toshiro, Tanaka, Ryojiro, Kobayashi, Hikaru, Ishida, Fumihiro, Hisanaga, Shuichi, Matsumoto, Masanori, Fujimura, Yoshihiro, Miyata, Toshiyuki
Vydáno 2014Text -
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Prognostic effects of treatment protocols for febrile convulsive status epilepticus in children Autor Tokumoto, Shoichi, Nishiyama, Masahiro, Yamaguchi, Hiroshi, Tomioka, Kazumi, Ishida, Yusuke, Toyoshima, Daisaku, Kurosawa, Hiroshi, Nozu, Kandai, Maruyama, Azusa, Tanaka, Ryojiro, Iijima, Kazumoto, Nagase, Hiroaki
Vydáno 2022Text -
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Early steroid pulse therapy for children with suspected acute encephalopathy: An observational study Autor Ishida, Yusuke, Nishiyama, Masahiro, Yamaguchi, Hiroshi, Tomioka, Kazumi, Takeda, Hiroki, Tokumoto, Shoichi, Toyoshima, Daisaku, Maruyama, Azusa, Seino, Yusuke, Aoki, Kazunori, Nozu, Kandai, Kurosawa, Hiroshi, Tanaka, Ryojiro, Iijima, Kazumoto, Nagase, Hiroaki
Vydáno 2021Text -
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Cyclosporine C(2) Monitoring for the Treatment of Frequently Relapsing Nephrotic Syndrome in Children: A Multicenter Randomized Phase II Trial Autor Iijima, Kazumoto, Sako, Mayumi, Oba, Mari Saito, Ito, Shuichi, Hataya, Hiroshi, Tanaka, Ryojiro, Ohwada, Yoko, Kamei, Koichi, Ishikura, Kenji, Yata, Nahoko, Nozu, Kandai, Honda, Masataka, Nakamura, Hidefumi, Nagata, Michio, Ohashi, Yasuo, Nakanishi, Koichi, Yoshikawa, Norishige
Vydáno 2014Text -
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Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases Autor Ishiko, Shinya, Horinouchi, Tomoko, Fujimaru, Rika, Shima, Yuko, Kaito, Hiroshi, Tanaka, Ryojiro, Ishimori, Shingo, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Yoshimura, Momoka, Nakanishi, Koichi, Fujimura, Junya, Kamiyoshi, Naohiro, Nagase, Hiroaki, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai
Vydáno 2020Text -
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Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population Autor Jia, Xiaoyuan, Horinouchi, Tomoko, Hitomi, Yuki, Shono, Akemi, Khor, Seik-Soon, Omae, Yosuke, Kojima, Kaname, Kawai, Yosuke, Nagasaki, Masao, Kaku, Yoshitsugu, Okamoto, Takayuki, Ohwada, Yoko, Ohta, Kazuhide, Okuda, Yusuke, Fujimaru, Rika, Hatae, Ken, Kumagai, Naonori, Sawanobori, Emi, Nakazato, Hitoshi, Ohtsuka, Yasufumi, Nakanishi, Koichi, Shima, Yuko, Tanaka, Ryojiro, Ashida, Akira, Kamei, Koichi, Ishikura, Kenji, Nozu, Kandai, Tokunaga, Katsushi, Iijima, Kazumoto
Vydáno 2018Text -
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Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome Autor Iijima, Kazumoto, Sako, Mayumi, Oba, Mari, Tanaka, Seiji, Hamada, Riku, Sakai, Tomoyuki, Ohwada, Yoko, Ninchoji, Takeshi, Yamamura, Tomohiko, Machida, Hiroyuki, Shima, Yuko, Tanaka, Ryojiro, Kaito, Hiroshi, Araki, Yoshinori, Morohashi, Tamaki, Kumagai, Naonori, Gotoh, Yoshimitsu, Ikezumi, Yohei, Kubota, Takuo, Kamei, Koichi, Fujita, Naoya, Ohtsuka, Yasufumi, Okamoto, Takayuki, Yamada, Takeshi, Tanaka, Eriko, Shimizu, Masaki, Horinochi, Tomoko, Konishi, Akihide, Omori, Takashi, Nakanishi, Koichi, Ishikura, Kenji, Ito, Shuichi, Nakamura, Hidefumi, Nozu, Kandai
Vydáno 2022Text -
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Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome Autor Jia, Xiaoyuan, Yamamura, Tomohiko, Gbadegesin, Rasheed, McNulty, Michelle T., Song, Kyuyong, Nagano, China, Hitomi, Yuki, Lee, Dongwon, Aiba, Yoshihiro, Khor, Seik-Soon, Ueno, Kazuko, Kawai, Yosuke, Nagasaki, Masao, Noiri, Eisei, Horinouchi, Tomoko, Kaito, Hiroshi, Hamada, Riku, Okamoto, Takayuki, Kamei, Koichi, Kaku, Yoshitsugu, Fujimaru, Rika, Tanaka, Ryojiro, Shima, Yuko, Baek, Jiwon, Kang, Hee Gyung, Ha, Il-Soo, Han, Kyoung Hee, Yang, Eun Mi, Abeyagunawardena, Asiri, Lane, Brandon, Chryst-Stangl, Megan, Esezobor, Christopher, Solarin, Adaobi, Dossier, Claire, Deschénes, Georges, Vivarelli, Marina, Debiec, Hanna, Ishikura, Kenji, Matsuo, Masafumi, Nozu, Kandai, Ronco, Pierre, Il Cheong, Hae, Sampson, Matthew G., Tokunaga, Katsushi, Iijima, Kazumoto
Vydáno 2020Text -
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Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment Autor Ashraf, Shazia, Kudo, Hiroki, Rao, Jia, Kikuchi, Atsuo, Widmeier, Eugen, Lawson, Jennifer A., Tan, Weizhen, Hermle, Tobias, Warejko, Jillian K., Shril, Shirlee, Airik, Merlin, Jobst-Schwan, Tilman, Lovric, Svjetlana, Braun, Daniela A., Gee, Heon Yung, Schapiro, David, Majmundar, Amar J., Sadowski, Carolin E., Pabst, Werner L., Daga, Ankana, van der Ven, Amelie T., Schmidt, Johanna M., Low, Boon Chuan, Gupta, Anjali Bansal, Tripathi, Brajendra K., Wong, Jenny, Campbell, Kirk, Metcalfe, Kay, Schanze, Denny, Niihori, Tetsuya, Kaito, Hiroshi, Nozu, Kandai, Tsukaguchi, Hiroyasu, Tanaka, Ryojiro, Hamahira, Kiyoshi, Kobayashi, Yasuko, Takizawa, Takumi, Funayama, Ryo, Nakayama, Keiko, Aoki, Yoko, Kumagai, Naonori, Iijima, Kazumoto, Fehrenbach, Henry, Kari, Jameela A., El Desoky, Sherif, Jalalah, Sawsan, Bogdanovic, Radovan, Stajić, Nataša, Zappel, Hildegard, Rakhmetova, Assel, Wassmer, Sharon-Rose, Jungraithmayr, Therese, Strehlau, Juergen, Kumar, Aravind Selvin, Bagga, Arvind, Soliman, Neveen A., Mane, Shrikant M., Kaufman, Lewis, Lowy, Douglas R., Jairajpuri, Mohamad A., Lifton, Richard P., Pei, York, Zenker, Martin, Kure, Shigeo, Hildebrandt, Friedhelm
Vydáno 2018Text