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Results: 1-10 |
Results: 10
Mutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions ofEPM2A gene
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
Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis
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
Oxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders
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
Electron correlations in double exchange model with orbital degeneracy
Authors: Imai, Y Kumada, S Kawakami, N
Citation: Y. Imai et al., Electron correlations in double exchange model with orbital degeneracy, PHYSICA B, 281, 2000, pp. 536-537
Reversible frontal lobe syndrome associated with influenza virus infectionin children
Authors: Sato, S Kumada, S Koji, T Okaniwa, M
Citation: S. Sato et al., Reversible frontal lobe syndrome associated with influenza virus infectionin children, PED NEUROL, 22(4), 2000, pp. 318-321
Nocturnal enuresis and the pontine reticular formation
Authors: Kohyama, J Kumada, S Shimohira, M Araki, S Itoh, M Iwakawa, Y
Citation: J. Kohyama et al., Nocturnal enuresis and the pontine reticular formation, EUR UROL, 38(5), 2000, pp. 631-634
The cerebellar and thalamic degeneration in Fukuyama-type congenital muscular dystrophy
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
Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophyand Machado-Joseph disease
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
Quantum phase transitions in two-dimensional spin systems with ladder, plaquette and mixed-spin structures
Authors: Koga, A Kumada, S Kawakami, N
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
Two-dimensional quantum spill systems with ladder and Plaquette structures
Authors: Koga, A Kumada, S Kawakami, N
Citation: A. Koga et al., Two-dimensional quantum spill systems with ladder and Plaquette structures, J PHYS JPN, 68(2), 1999, pp. 642-649
Risultati: 1-10 |