M. Yasuda
Hyogo Institute for Aging Brain and Cognitive Disorders
Himeji
Japan
Name/email consistency: high
- Novel presenilin-1 mutation with widespread cortical amyloid deposition but limited cerebral amyloid angiopathy. Yasuda, M., Maeda, S., Kawamata, T., Tamaoka, A., Yamamoto, Y., Kuroda, S., Maeda, K., Tanaka, C. J. Neurol. Neurosurg. Psychiatr. (2000)
- A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation. Yasuda, M., Yokoyama, K., Nakayasu, T., Nishimura, Y., Matsui, M., Yokoyama, T., Miyoshi, K., Tanaka, C. Neurology (2000)
- A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2. Yasuda, M., Maeda, K., Hashimoto, M., Yamashita, H., Ikejiri, Y., Bird, T.D., Tanaka, C., Schellenberg, G.D. Arch. Neurol. (1999)
- Apolipoprotein E epsilon 4 allele and whole brain atrophy in late-onset Alzheimer's disease. Yasuda, M., Mori, E., Kitagaki, H., Yamashita, H., Hirono, N., Shimada, K., Maeda, K., Tanaka, C. Am. J. Psychiatry (1998)
- A novel missense mutation in the presenilin-1 gene in a familial Alzheimer's disease pedigree with abundant amyloid angiopathy. Yasuda, M., Maeda, K., Ikejiri, Y., Kawamata, T., Kuroda, S., Tanaka, C. Neurosci. Lett. (1997)
