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Results: 1-12 |
Results: 12

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: Itoh, Y Yamada, M Sodeyama, N Suematsu, N Matsushita, M Otomo, E Mizusawa, H
Citation: Y. Itoh et al., Atherosclerosis is not implicated in association of APOE epsilon 4 with AD, NEUROLOGY, 53(1), 1999, pp. 236-237

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

Authors: Yoshida, R Otomo, E
Citation: R. Yoshida et E. Otomo, PVH in MRI of multi-infarct dementia, 1ST INTERNATIONAL CONGRESS ON VASCULAR DEMENTIA, 1999, pp. 201-204
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