Authors:
Ganesh, S
Shoda, K
Amano, K
Uchiyama, A
Kumada, S
Moriyama, N
Hirose, S
Yamakawa, K
Citation: S. Ganesh et al., Mutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions ofEPM2A gene, MOL CELL PR, 15(5), 2001, pp. 281-289
Authors:
Kumada, S
Hayashi, M
Kenmochi, J
Kurosawa, S
Shimozawa, N
Kratz, LE
Kelley, RI
Taki, K
Okaniwa, M
Citation: S. Kumada et al., Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis, AM J MED G, 98(3), 2001, pp. 250-255
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:
Kumada, S
Tsuchiya, K
Takahashi, M
Takesue, M
Shiotsu, H
Nomura, Y
Segawa, M
Ikeda, K
Hayashi, M
Citation: S. Kumada et al., The cerebellar and thalamic degeneration in Fukuyama-type congenital muscular dystrophy, ACT NEUROP, 99(2), 2000, pp. 209-213
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
Citation: A. Koga et al., Quantum phase transitions in two-dimensional spin systems with ladder, plaquette and mixed-spin structures, J PHYS JPN, 68(7), 1999, pp. 2373-2379