Aoki M - Search Results

1

Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations.

Abe K, Aoki M, Ikeda M, Watanabe M, Hirai S, Itoyama Y. Abe K, et al. Among authors: aoki m. J Neurol Sci. 1996 Mar;136(1-2):108-16. doi: 10.1016/0022-510x(95)00314-r. J Neurol Sci. 1996. PMID: 8815157 Clinical Trial.

2

Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase gene.

Ikeda M, Abe K, Aoki M, Sahara M, Watanabe M, Shoji M, St George-Hyslop PH, Hirai S, Itoyama Y. Ikeda M, et al. Among authors: aoki m. Neurology. 1995 Nov;45(11):2038-42. doi: 10.1212/wnl.45.11.2038. Neurology. 1995. PMID: 7501156

3

Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation.

Aoki M, Abe K, Houi K, Ogasawara M, Matsubara Y, Kobayashi T, Mochio S, Narisawa K, Itoyama Y. Aoki M, et al. Ann Neurol. 1995 May;37(5):676-9. doi: 10.1002/ana.410370518. Ann Neurol. 1995. PMID: 7755363

4

A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis.

Ikeda M, Abe K, Aoki M, Ogasawara M, Kameya T, Watanabe M, Shoji M, Hirai S, Itoyama Y. Ikeda M, et al. Among authors: aoki m. Hum Mol Genet. 1995 Mar;4(3):491-2. doi: 10.1093/hmg/4.3.491. Hum Mol Genet. 1995. PMID: 7795609 No abstract available.

5

Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS.

Aoki M, Ogasawara M, Matsubara Y, Narisawa K, Nakamura S, Itoyama Y, Abe K. Aoki M, et al. J Neurol Sci. 1994 Oct;126(1):77-83. doi: 10.1016/0022-510x(94)90097-3. J Neurol Sci. 1994. PMID: 7836951

6

Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease.

Watanabe M, Abe K, Aoki M, Kameya T, Kaneko J, Shoji M, Ikeda M, Shizuka M, Ikeda Y, Iizuka T, Hirai S, Itoyama Y. Watanabe M, et al. Among authors: aoki m. J Neurol Sci. 1996 Mar;136(1-2):101-7. doi: 10.1016/0022-510x(95)00307-n. J Neurol Sci. 1996. PMID: 8815156

7

Inductions of Cu/Zn superoxide dismutase- and nitric oxide synthase-like immunoreactivities in rabbit spinal cord after transient ischemia.

Watanabe M, Sakurai M, Abe K, Aoki M, Sadahiro M, Tabayashi K, Okamoto K, Shoji M, Itoyama Y. Watanabe M, et al. Among authors: aoki m. Brain Res. 1996 Sep 2;732(1-2):69-74. doi: 10.1016/0006-8993(96)00490-8. Brain Res. 1996. PMID: 8891270

8

A novel two-base mutation in the Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan.

Morita M, Aoki M, Abe K, Hasegawa T, Sakuma R, Onodera Y, Ichikawa N, Nishizawa M, Itoyama Y. Morita M, et al. Among authors: aoki m. Neurosci Lett. 1996 Feb 23;205(2):79-82. doi: 10.1016/0304-3940(96)12378-8. Neurosci Lett. 1996. PMID: 8907321

9

[Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations in Japan].

Hasegawa T, Abe K, Aoki M, Itoyama Y. Hasegawa T, et al. Among authors: aoki m. Nihon Rinsho. 1996 Nov;54(11):3157-62. Nihon Rinsho. 1996. PMID: 8950969 Review. Japanese. No abstract available.

10

A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familial motor neuron disease.

Watanabe M, Aoki M, Abe K, Shoji M, Iizuka T, Ikeda Y, Hirai S, Kurokawa K, Kato T, Sasaki H, Itoyama Y. Watanabe M, et al. Among authors: aoki m. Hum Mutat. 1997;9(1):69-71. doi: 10.1002/(SICI)1098-1004(1997)9:1<69::AID-HUMU14>3.0.CO;2-N. Hum Mutat. 1997. PMID: 8990014 No abstract available.

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