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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Ikuyo Ueda

Department of Pediatrics

Kyoto Prefectural University of Medicine




Name/email consistency: high



  • Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan. 2006 - 2007
  • Department of Paediatrics, and Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan. 2003


  1. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations. Ueda, I., Kurokawa, Y., Koike, K., Ito, S., Sakata, A., Matsumora, T., Fukushima, T., Morimoto, A., Ishii, E., Imashuku, S. Am. J. Hematol. (2007) [Pubmed]
  2. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL). Ueda, I., Ishii, E., Morimoto, A., Ohga, S., Sako, M., Imashuku, S. Pediatr. Blood. Cancer (2006) [Pubmed]
  3. A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosis. Ueda, I., Kohdera, U., Hibi, S., Inaba, T., Yamamoto, K., Sugimoto, T., Morimoto, A., Ishii, E., Imashuku, S. Int. J. Hematol. (2006) [Pubmed]
  4. Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan. Ueda, I., Morimoto, A., Inaba, T., Yagi, T., Hibi, S., Sugimoto, T., Sako, M., Yanai, F., Fukushima, T., Nakayama, M., Ishii, E., Imashuku, S. Br. J. Haematol. (2003) [Pubmed]
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