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Results: 1-16 |
Results: 16
Activated brain regions in musicians during an ensemble: a PET study
Authors: Satoh, M Takeda, K Nagata, K Hatazawa, J Kuzuhara, S
Citation: M. Satoh et al., Activated brain regions in musicians during an ensemble: a PET study, COGN BRAIN, 12(1), 2001, pp. 101-108
Cerebral atrophy and convulsive seizures after recovery from cerebral edema and coma in a patient with fulminant hepatitis B
Authors: Honda, S Taniguchi, A Murai, K Kuzuhara, S
Citation: S. Honda et al., Cerebral atrophy and convulsive seizures after recovery from cerebral edema and coma in a patient with fulminant hepatitis B, INTERN MED, 40(3), 2001, pp. 255-258
Large-scale, multicenter study of cerebrospinal fluid tau protein phosphorylated at serine 199 for the antemortem diagnosis of Alzheimer's disease
Authors: Itoh, N Arai, H Urakami, K Ishiguro, K Ohno, H Hampel, H Buerger, K Wiltfang, J Otto, M Kretzschmar, H Moeller, HJ Imagawa, M Kohno, H Nakashima, K Kuzuhara, S Sasaki, H Imahori, K
Citation: N. Itoh et al., Large-scale, multicenter study of cerebrospinal fluid tau protein phosphorylated at serine 199 for the antemortem diagnosis of Alzheimer's disease, ANN NEUROL, 50(2), 2001, pp. 150-156
Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii peninsula of Japan: Clinical and neuropathological study and tau analysis
Authors: Kuzuhara, S Kokubo, Y Sasaki, R Narita, Y Yabana, T Hasegawa, M Iwatsubo, T
Citation: S. Kuzuhara et al., Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii peninsula of Japan: Clinical and neuropathological study and tau analysis, ANN NEUROL, 49(4), 2001, pp. 501-511
A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotoniacongenita
Authors: Sasaki, R Ito, N Shimamura, M Murakami, T Kuzuhara, S Uchino, M Uyama, E
Citation: R. Sasaki et al., A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotoniacongenita, MUSCLE NERV, 24(3), 2001, pp. 357-363
Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification
Authors: Yamamura, Y Hattori, N Matsumine, H Kuzuhara, S Mizuno, Y
Citation: Y. Yamamura et al., Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification, BRAIN DEVEL, 2000, pp. S87-S91
Geographical distribution of amyotrophic lateral sclerosis with neurofibrillary tangles in the Kii peninsula of Japan
Authors: Kokubo, Y Kuzuhara, S Narita, Y
Citation: Y. Kokubo et al., Geographical distribution of amyotrophic lateral sclerosis with neurofibrillary tangles in the Kii peninsula of Japan, J NEUROL, 247(11), 2000, pp. 850-852
Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course
Authors: Saito, Y Kawai, M Inoue, K Sasaki, R Arai, H Nanba, E Kuzuhara, S Ihara, Y Kanazawa, I Murayama, S
Citation: Y. Saito et al., Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course, J NEUR SCI, 177(1), 2000, pp. 48-59
Input-output organization of the foot motor area in humans
Authors: Machii, K Ugawa, Y Terao, Y Hanajima, R Furubayashi, T Mochizuki, H Shiio, Y Enomoto, H Uesugi, H Kuzuhara, S Kanazawa, I
Citation: K. Machii et al., Input-output organization of the foot motor area in humans, CLIN NEU, 110(7), 1999, pp. 1315-1320
Apolipoprotein E phenotypes in healthy normal controls and demented subjects with Alzheimer's disease and vascular dementia in Mie Prefecture of Japan
Authors: Nakayama, S Kuzuhara, S
Citation: S. Nakayama et S. Kuzuhara, Apolipoprotein E phenotypes in healthy normal controls and demented subjects with Alzheimer's disease and vascular dementia in Mie Prefecture of Japan, PSY CLIN N, 53(6), 1999, pp. 643-648
Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia
Authors: Sasaki, R Ichiyasu, H Ito, N Ikeda, T Takano, H Ikeuchi, T Kuzuhara, S Uchino, M Tsuji, S Uyama, E
Citation: R. Sasaki et al., Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia, NEUROMUSC D, 9(8), 1999, pp. 587-592
A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg
Authors: Sasaki, R Takano, H Kamakura, K Kaida, K Hirata, A Saito, M Tanaka, H Kuzuhara, S Tsuji, S
Citation: R. Sasaki et al., A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg, ARCH NEUROL, 56(6), 1999, pp. 692-696
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting
Authors: Shimizu, S Hoshi, K Muramoto, T Homma, M Ironside, JW Kuzuhara, S Sato, T Yamamoto, T Kitamoto, T
Citation: S. Shimizu et al., Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting, ARCH NEUROL, 56(3), 1999, pp. 357-362
Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation
Authors: Kokubo, Y Kuzuhara, S Narita, Y Kikugawa, K Nakano, R Inuzuka, T Tsuji, S Watanabe, M Miyazaki, T Murayama, S Ihara, Y
Citation: Y. Kokubo et al., Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation, ARCH NEUROL, 56(12), 1999, pp. 1506-1508
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
Authors: Hattori, N Kitada, T Matsumine, H Asakawa, S Yamamura, Y Yoshino, H Kobayashi, T Yokochi, M Wang, M Yoritaka, A Kondo, T Kuzuhara, S Nakamura, S Shimizu, N Mizuno, Y
Citation: N. Hattori et al., Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals, ANN NEUROL, 44(6), 1998, pp. 935-941
A novel de novo point mutation in the GTP cyclohydrolase I gene in a Japanese patient with hereditary progressive and dopa responsive dystonia
Authors: Sasaki, R Naito, Y Kuzuhara, S
Citation: R. Sasaki et al., A novel de novo point mutation in the GTP cyclohydrolase I gene in a Japanese patient with hereditary progressive and dopa responsive dystonia, J NE NE PSY, 65(6), 1998, pp. 947-947
Risultati: 1-16 |