Authors: Minami, N Ikezoe, K Kuroda, H Nakabayashi, H Satoyoshi, E Nonaka, I

Citation: N. Minami et al., Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy, NEUROMUSC D, 11(8), 2001, pp. 699-702

Authors: Nakagawa, M Miyagoe-Suzuki, Y Ikezoe, K Miyata, Y Nonaka, I Harii, K Takeda, S

Citation: M. Nakagawa et al., Schwann cell myelination occurred without basal lamina formation in laminin alpha 2 chain-null mutant (dy(3K)/dy(3K)) mice, GLIA, 35(2), 2001, pp. 101-110

Authors: Yan, CZ Ikezoe, K Nonaka, I

Citation: Cz. Yan et al., Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles, ACT NEUROP, 101(1), 2001, pp. 9-16

Authors: Ikezoe, K Yan, CZ Momoi, T Imoto, C Minami, N Ariga, M Nihei, K Nonaka, I

Citation: K. Ikezoe et al., A novel congenital myopathy with apoptotic changes, ANN NEUROL, 47(4), 2000, pp. 531-536

Authors: Ikezoe, K Yoshimura, T Taniwaki, T Matsuura, E Furuya, H Yamada, T Nagamatsu, K Kira, J

Citation: K. Ikezoe et al., Autosomal dominant familial spinal and bulbar muscular atrophy with gynecomastia, NEUROLOGY, 53(9), 1999, pp. 2187-2189

Authors: Minami, N Nishino, I Kobayashi, O Ikezoe, K Goto, Y Nonaka, I

Citation: N. Minami et al., Mutations of calpain 3 gene in patients with sporadic limb-girdle musculardystrophy in Japan, J NEUR SCI, 171(1), 1999, pp. 31-37