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Results: 1-6 |
Results: 6

Authors: Hayashi, M Itoh, M Araki, S Kumada, S Shioda, K Tamagawa, K Mizutani, T Morimatsu, Y Minagawa, M Oda, M
Citation: M. Hayashi et al., Oxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders, J NE EXP NE, 60(4), 2001, pp. 350-356

Authors: Tsuchiya, K Ikeda, K Haga, C Kobayashi, T Morimatsu, Y Nakano, I Matsushita, M
Citation: K. Tsuchiya et al., Atypical amyotrophic lateral sclerosis with dementia mimicking frontal Pick's disease: a report of an autopsy case with a clinical course of 15 years, ACT NEUROP, 101(6), 2001, pp. 625-630

Authors: Kumada, S Hayashi, M Mizuguchi, M Nakano, I Morimatsu, Y Oda, M
Citation: S. Kumada et al., Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophyand Machado-Joseph disease, ACT NEUROP, 99(1), 2000, pp. 48-54

Authors: Itoh, M Hayashi, M Shioda, K Minagawa, M Isa, F Tamagawa, K Morimatsu, Y Oda, M
Citation: M. Itoh et al., Neurodegeneration in hereditary nucleotide repair disorders, BRAIN DEVEL, 21(5), 1999, pp. 326-333

Authors: Kurata, K Hayashi, M Satoh, J Kojima, H Nagata, J Tamagawa, K Shinohara, T Morimatsu, Y Kominami, E
Citation: K. Kurata et al., Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosis, BRAIN DEVEL, 21(1), 1999, pp. 63-67

Authors: Araki, S Hayashi, M Suzuki, K Nagata, J Kurata, K Morimatsu, Y Matsuyama, H
Citation: S. Araki et al., Immunohistochemical evaluation of the marbled state in childhood hypoxic encephalopathy, ACT NEUROP, 98(3), 1999, pp. 257-261
Risultati: 1-6 |