Yusei Shiga
Department of Neurology
Tohoku University Graduate School of Medicine
1-1 Seiryo-machi
Aoba-ku
Japan
Name/email consistency: high
- Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution. Shiga, Y., Satoh, K., Kitamoto, T., Kanno, S., Nakashima, I., Sato, S., Fujihara, K., Takata, H., Nobukuni, K., Kuroda, S., Takano, H., Umeda, Y., Konno, H., Nagasato, K., Satoh, A., Matsuda, Y., Hidaka, M., Takahashi, H., Sano, Y., Kim, K., Konishi, T., Doh-ura, K., Sato, T., Sasaki, K., Nakamura, Y., Yamada, M., Mizusawa, H., Itoyama, Y. J. Neurol. (2007)
- 14-3-3 protein levels and isoform patterns in the cerebrospinal fluid of Creutzfeldt-Jakob disease patients in the progressive and terminal stages. Shiga, Y., Wakabayashi, H., Miyazawa, K., Kido, H., Itoyama, Y. J. Clin. Neurosci (2006)
- Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Shiga, Y., Miyazawa, K., Sato, S., Fukushima, R., Shibuya, S., Sato, Y., Konno, H., Doh-ura, K., Mugikura, S., Tamura, H., Higano, S., Takahashi, S., Itoyama, Y. Neurology (2004)









