Authors:
Yamada, M
Itoh, Y
Sodeyama, N
Suematsu, N
Otomo, E
Matsushita, M
Mizusawa, H
Citation: M. Yamada et al., Senile dementia of the neurofibrillary tangle type: A comparison with Alzheimer's disease, DEMENT G C, 12(2), 2001, pp. 117-126
Authors:
Sodeyama, N
Mizusawa, H
Yamada, M
Itoh, Y
Otomo, E
Matsushita, M
Citation: N. Sodeyama et al., Lack of association of neprilysin polymorphism with Alzheimer's disease and Alzheimer's disease-type neuropathological changes, J NE NE PSY, 71(6), 2001, pp. 817-818
Authors:
Sodeyama, N
Iwata, T
Ishikawa, K
Mizusawa, H
Yamada, M
Itoh, Y
Otomo, E
Matsushita, M
Komatsuzaki, Y
Citation: N. Sodeyama et al., Very early onset Alzheimer's disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile), J NE NE PSY, 71(4), 2001, pp. 556-557
Authors:
Sodeyama, N
Yamada, M
Itoh, Y
Suematsu, N
Matsushita, M
Otomo, E
Mizusawa, H
Citation: N. Sodeyama et al., alpha 2-macroglobulin polymorphism is not associated with AD or AD-type neuropathology in the Japanese, NEUROLOGY, 54(2), 2000, pp. 443-446
Authors:
Sodeyama, N
Yamada, M
Itoh, Y
Suematsu, N
Matsushita, M
Otomo, E
Mizusawa, H
Citation: N. Sodeyama et al., Lack of genetic associations of alpha-1-antichymotrypsin polymorphism withAlzheimer-type neuropathological changes or sporadic Alzheimer's disease, DEMENT G C, 10(3), 1999, pp. 221-225
Authors:
Yamada, M
Sodeyama, N
Itoh, Y
Suematsu, N
Otomo, E
Matsushita, M
Mizusawa, H
Citation: M. Yamada et al., A deletion polymorphism of alpha(2)-macroglobulin gene and cerebral amyloid angiopathy, STROKE, 30(11), 1999, pp. 2277-2279
Authors:
Sodeyama, N
Yamada, M
Itoh, Y
Suematsu, N
Matsushita, M
Otomo, E
Mizusawa, H
Citation: N. Sodeyama et al., No association of paraoxonase gene polymorphism with atherosclerosis or Alzheimer's disease, NEUROLOGY, 53(5), 1999, pp. 1146-1148
Authors:
Yamada, M
Itoh, Y
Inaba, A
Wada, Y
Takashima, M
Satoh, S
Kamata, T
Okeda, R
Kayano, T
Suematsu, N
Kitamoto, T
Otomo, E
Matsushita, M
Mizusawa, H
Citation: M. Yamada et al., An inherited prion disease with a PrPP105L mutation - Clinicopathologic and PrP heterogeneity, NEUROLOGY, 53(1), 1999, pp. 181-188
Authors:
Yamada, M
Tomimitsu, H
Yokota, T
Tomi, H
Sunohara, N
Mukoyama, N
Itoh, Y
Suematsu, N
Otomo, E
Okeda, R
Matsushita, M
Mizusawa, H
Citation: M. Yamada et al., Involvement of the spinal posterior horn in Gerstmann-Straussler-Scheinkerdisease (PrP P102L), NEUROLOGY, 52(2), 1999, pp. 260-265
Authors:
Sodeyama, N
Yamada, M
Mizusawa, H
Itoh, Y
Otomo, E
Suematsu, N
Matsushita, M
Citation: N. Sodeyama et al., Association between butyrylcholinesterase K variant and the Alzheimer typeneuropathological changes in apolipoprotein E epsilon 4 carriers older than 75 years, J NE NE PSY, 67(5), 1999, pp. 693-694