Watanabe 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: watanabe 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

Induction of nitrotyrosine-like immunoreactivity in the lower motor neuron of amyotrophic lateral sclerosis.

Abe K, Pan LH, Watanabe M, Kato T, Itoyama Y. Abe K, et al. Among authors: watanabe m. Neurosci Lett. 1995 Oct 20;199(2):152-4. doi: 10.1016/0304-3940(95)12039-7. Neurosci Lett. 1995. PMID: 8584246

3

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. J Neurol Sci. 1996 Mar;136(1-2):101-7. doi: 10.1016/0022-510x(95)00307-n. J Neurol Sci. 1996. PMID: 8815156

4

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. Brain Res. 1996 Sep 2;732(1-2):69-74. doi: 10.1016/0006-8993(96)00490-8. Brain Res. 1996. PMID: 8891270

5

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. 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.

6

Upregulation of protein-tyrosine nitration in the anterior horn cells of amyotrophic lateral sclerosis.

Abe K, Pan LH, Watanabe M, Konno H, Kato T, Itoyama Y. Abe K, et al. Among authors: watanabe m. Neurol Res. 1997 Apr;19(2):124-8. doi: 10.1080/01616412.1997.11740784. Neurol Res. 1997. PMID: 9175139

7

Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis.

Shizuka M, Watanabe M, Aoki M, Ikeda Y, Mizushima K, Okamoto K, Itoyama Y, Abe K, Shoji M. Shizuka M, et al. Among authors: watanabe m. J Neurol Sci. 1997 Sep 10;150(2):133-5. doi: 10.1016/s0022-510x(97)00067-1. J Neurol Sci. 1997. PMID: 9268240

8

Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics.

Mizushima K, Watanabe M, Abe K, Aoki M, Itoyama Y, Shizuka M, Okamoto K, Shoji M. Mizushima K, et al. Among authors: watanabe m. J Neurol Sci. 1998 Apr 1;156(2):180-5. doi: 10.1016/s0022-510x(98)00040-9. J Neurol Sci. 1998. PMID: 9588855

9

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: watanabe m. Neurology. 1995 Nov;45(11):2038-42. doi: 10.1212/wnl.45.11.2038. Neurology. 1995. PMID: 7501156

10

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: watanabe 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.

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