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Results: 1-3 |
Results: 3
Complete skipping of exon 66 due to novel mutations of the dystrophin genewas identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
Authors: Wibawa, T Takeshima, Y Mitsuyoshi, I Wada, H Surono, A Nakamura, H Matsuo, M
Citation: T. Wibawa et al., Complete skipping of exon 66 due to novel mutations of the dystrophin genewas identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation, BRAIN DEVEL, 22(2), 2000, pp. 107-112
Congenital fiber type disproportion: Severe form with marked improvement
Authors: Tsuji, M Higuchi, T Shiraishi, K Mitsuyoshi, I Hattori, H
Citation: M. Tsuji et al., Congenital fiber type disproportion: Severe form with marked improvement, PED NEUROL, 21(3), 1999, pp. 658-660
A case of epileptic negative myoclonus: therapeutic considerations
Authors: Shirasaka, Y Mitsuyoshi, I
Citation: Y. Shirasaka et I. Mitsuyoshi, A case of epileptic negative myoclonus: therapeutic considerations, BRAIN DEVEL, 21(3), 1999, pp. 209-212
Risultati: 1-3 |