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Results: 1-11 |
Results: 11
Alcohol dehydrogenase polymorphism and Parkinson's disease
Authors: Tan, EK Nagamitsu, S Matsuura, T Khajavi, M Jankovic, J Ondo, W Ashizawa, T
Citation: Ek. Tan et al., Alcohol dehydrogenase polymorphism and Parkinson's disease, NEUROSCI L, 305(1), 2001, pp. 70-72
Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasms
Authors: Nagamitsu, S Matsuishi, T Yamashita, Y Shimizu, T Iwanaga, R Murakami, Y Miyazaki, M Hashimoto, T Kato, H
Citation: S. Nagamitsu et al., Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasms, J NEURAL TR, 108(3), 2001, pp. 363-371
Variability and validity of polymorphism association studies in Parkinson's disease
Authors: Tan, EK Khajavi, M Thornby, JI Nagamitsu, S Jankovic, J Ashizawa, T
Citation: Ek. Tan et al., Variability and validity of polymorphism association studies in Parkinson's disease, NEUROLOGY, 55(4), 2000, pp. 533-538
A "dystrophic" variant of autosomal recessive myotonia congenita caused bynovel mutations in the CLCN1 gene
Authors: Nagamitsu, S Matsuura, T Khajavi, M Armstrong, R Gooch, C Harati, Y Ashizawa, T
Citation: S. Nagamitsu et al., A "dystrophic" variant of autosomal recessive myotonia congenita caused bynovel mutations in the CLCN1 gene, NEUROLOGY, 55(11), 2000, pp. 1697-1703
Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?
Authors: Tan, EK Matsuura, T Nagamitsu, S Khajavi, M Jankovic, J Ashizawa, T
Citation: Ek. Tan et al., Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?, NEUROLOGY, 54(5), 2000, pp. 1195-1198
Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome
Authors: Obata, K Matsuishi, T Yamashita, Y Fukuda, T Kuwajima, K Horiuchi, I Nagamitsu, S Iwanaga, R Kimura, A Omori, I Endo, S Mori, K Kondo, I
Citation: K. Obata et al., Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome, J MED GENET, 37(8), 2000, pp. 608-610
Multicenter study of paroxysmal dyskinesias in Japan - Clinical and pedigree analysis
Authors: Nagamitsu, S Matsuishi, T Hashimoto, K Yamashita, Y Aihara, M Shimizu, K Mizuguchi, M Iwamoto, H Saitoh, S Hirano, Y Kato, H Fukuyama, Y Shimada, M
Citation: S. Nagamitsu et al., Multicenter study of paroxysmal dyskinesias in Japan - Clinical and pedigree analysis, MOVEMENT D, 14(4), 1999, pp. 658-663
Increased cerebrospinal fluid levels of substance P in patients with amyotrophic lateral sclerosis
Authors: Matsuishi, T Nagamitsu, S Shoji, H Itoh, M Takashima, S Iwaki, T Shida, N Yamashita, Y Sakai, T Kato, H
Citation: T. Matsuishi et al., Increased cerebrospinal fluid levels of substance P in patients with amyotrophic lateral sclerosis, J NEURAL TR, 106(9-10), 1999, pp. 943-948
Extrapontine myelinolysis with parkinsonism after rapid correction of hyponatremia: high cerebrospinal fluid level of homovanillic acid and successful dopaminergic treatment
Authors: Nagamitsu, S Matsuishi, T Yamashita, Y Yamada, S Kato, H
Citation: S. Nagamitsu et al., Extrapontine myelinolysis with parkinsonism after rapid correction of hyponatremia: high cerebrospinal fluid level of homovanillic acid and successful dopaminergic treatment, J NEURAL TR, 106(9-10), 1999, pp. 949-953
Decreased cerebellar blood flow in postinfectious acute cerebellar ataxia
Authors: Nagamitsu, S Matsuishi, T Ishibashi, M Yamashita, Y Nishimi, T Ichikawa, K Yamanishi, K Kato, H
Citation: S. Nagamitsu et al., Decreased cerebellar blood flow in postinfectious acute cerebellar ataxia, J NE NE PSY, 67(1), 1999, pp. 109-112
Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1
Authors: Tomita, H Nagamitsu, S Wakui, K Fukushima, Y Yamada, K Sadamatsu, M Masui, A Konishi, T Matsuishi, T Aihara, M Shimizu, K Hashimoto, K Mineta, M Matsushima, M Tsujita, T Saito, M Tanaka, H Tsuji, S Takagi, T Nakamura, Y Nanko, S Kato, N Nakane, Y Niikawa, N
Citation: H. Tomita et al., Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1, AM J HU GEN, 65(6), 1999, pp. 1688-1697
Risultati: 1-11 |