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Ikuyo Ueda

Department of Pediatrics

Kyoto Prefectural University of Medicine

Kyoto

Japan

[email]@*.kpu-m.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • 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

References

  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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