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Results: 1-10 |
Results: 10
Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)
Authors: Asaka, T Ikeuchi, K Okino, S Takizawa, Y Satake, R Nitta, E Komai, K Endo, K Higuchi, S Oyake, T Yoshimura, T Suenaga, A Uyama, E Saito, T Konagaya, M Sunohara, N Namba, R Takada, H Honke, K Nishina, M Tanaka, H Shinagawa, M Tanaka, K Matsushima, A Tsuji, S Takamori, M
Citation: T. Asaka et al., Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy), J HUM GENET, 46(11), 2001, pp. 649-655
Citrullinemia type II in a 64-year-old man with fluctuating serum citrulline levels
Authors: Maruyama, H Ogawa, M Nishio, T Kobayashi, K Saheki, T Sunohara, N
Citation: H. Maruyama et al., Citrullinemia type II in a 64-year-old man with fluctuating serum citrulline levels, J NEUR SCI, 182(2), 2001, pp. 167-170
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene - Reply
Authors: Arima, K Sunohara, N
Citation: K. Arima et N. Sunohara, Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene - Reply, NEUROLOGY, 55(12), 2000, pp. 1939-1939
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene
Authors: Arima, K Kowalska, A Hasegawa, M Mukoyama, M Watanabe, R Kawai, M Takahashi, K Iwatsubo, T Tabira, T Sunohara, N
Citation: K. Arima et al., Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene, NEUROLOGY, 54(9), 2000, pp. 1787-1795
SPECT image analysis using statistical parametric mapping in patients withParkinson's disease
Authors: Imon, Y Matsuda, H Ogawa, M Kogure, D Sunohara, N
Citation: Y. Imon et al., SPECT image analysis using statistical parametric mapping in patients withParkinson's disease, J NUCL MED, 40(10), 1999, pp. 1583-1589
Involvement of the spinal posterior horn in Gerstmann-Straussler-Scheinkerdisease (PrP P102L)
Authors: Yamada, M Tomimitsu, H Yokota, T Tomi, H Sunohara, N Mukoyama, N Itoh, Y Suematsu, N Otomo, E Okeda, R Matsushita, M Mizusawa, H
Citation: M. Yamada et al., Involvement of the spinal posterior horn in Gerstmann-Straussler-Scheinkerdisease (PrP P102L), NEUROLOGY, 52(2), 1999, pp. 260-265
Cellular co-localization of phosphorylated tau- and NACP/alpha-synuclein-epitopes in Lewy bodies in sporadic Parkinson's disease and in dementia withLewy bodies
Authors: Arima, K Hirai, S Sunohara, N Aoto, K Izumiyama, Y Ueda, K Ikeda, K Kawai, M
Citation: K. Arima et al., Cellular co-localization of phosphorylated tau- and NACP/alpha-synuclein-epitopes in Lewy bodies in sporadic Parkinson's disease and in dementia withLewy bodies, BRAIN RES, 843(1-2), 1999, pp. 53-61
Immunohistochemical and ultrastructural characterization of neuritic clusters around ghost tangles in the hippocampal formation in progressive supranuclear palsy brains
Authors: Arima, K Nakamura, M Sunohara, N Nishio, T Ogawa, M Hirai, S Kawai, M Ikeda, K
Citation: K. Arima et al., Immunohistochemical and ultrastructural characterization of neuritic clusters around ghost tangles in the hippocampal formation in progressive supranuclear palsy brains, ACT NEUROP, 97(6), 1999, pp. 565-576
Spinocerebellar ataxia type 6 in relation to CAG repeat length
Authors: Kaseda, Y Kawakami, H Matsuyama, Z Kumagai, R Toji, M Komure, O Nishimura, M Izumi, Y Udaka, F Kameyama, M Nishio, T Sunohara, N Kuroda, Y Nakamura, S
Citation: Y. Kaseda et al., Spinocerebellar ataxia type 6 in relation to CAG repeat length, ACT NEUR SC, 99(4), 1999, pp. 209-212
Myophosphorylase deficiency and limb-girdle muscular dystrophy in the samepedigree
Authors: Nishio, T Sunohara, N Nonaka, I Tsujino, S Sugie, H
Citation: T. Nishio et al., Myophosphorylase deficiency and limb-girdle muscular dystrophy in the samepedigree, ACT NEUR SC, 98(5), 1998, pp. 364-367
Risultati: 1-10 |