Ikuyo Ueda
Department of Pediatrics
Kyoto Prefectural University of Medicine
Kyoto
Japan
Name/email consistency: high
- 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)
- 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)
- 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)
- 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)