Watanabe M - Search Results

1

Oculomotor nuclear pathology in amyotrophic lateral sclerosis.

Okamoto K, Hirai S, Amari M, Iizuka T, Watanabe M, Murakami N, Takatama M. Okamoto K, et al. Among authors: watanabe m. Acta Neuropathol. 1993;85(5):458-62. doi: 10.1007/BF00230482. Acta Neuropathol. 1993. PMID: 8493857

2

Bunina bodies in amyotrophic lateral sclerosis immunostained with rabbit anti-cystatin C serum.

Okamoto K, Hirai S, Amari M, Watanabe M, Sakurai A. Okamoto K, et al. Among authors: watanabe m. Neurosci Lett. 1993 Nov 12;162(1-2):125-8. doi: 10.1016/0304-3940(93)90576-7. Neurosci Lett. 1993. PMID: 8121614

3

Reexamination of granulovacuolar degeneration.

Okamoto K, Hirai S, Iizuka T, Yanagisawa T, Watanabe M. Okamoto K, et al. Among authors: watanabe m. Acta Neuropathol. 1991;82(5):340-5. doi: 10.1007/BF00296544. Acta Neuropathol. 1991. PMID: 1722607

4

Genetic analysis of the cystatin C gene in familial and sporadic ALS patients.

Watanabe M, Jackson M, Ikeda M, Mizushima K, Amari M, Takatama M, Hirai S, Ikeda Y, Shizuka-Ikeda M, Okamoto K. Watanabe M, et al. Brain Res. 2006 Feb 16;1073-1074:20-4. doi: 10.1016/j.brainres.2005.12.046. Epub 2006 Jan 26. Brain Res. 2006. PMID: 16443201

5

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.

6

Accumulation of NACP/alpha-synuclein in lewy body disease and multiple system atrophy.

Shoji M, Harigaya Y, Sasaki A, Uéda K, Ishiguro K, Matsubara E, Watanabe M, Ikeda M, Kanai M, Tomidokoro Y, Shizuka M, Amari M, Kosaka K, Nakazato Y, Okamoto K, Hirai S. Shoji M, et al. Among authors: watanabe m. J Neurol Neurosurg Psychiatry. 2000 May;68(5):605-8. doi: 10.1136/jnnp.68.5.605. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766891 Free PMC article.

7

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

8

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.

9

Fundamental morphological changes in human olivary hypertrophy.

Okamoto K, Hirai S, Iizuka T, Watanabe M. Okamoto K, et al. Among authors: watanabe m. Acta Pathol Jpn. 1992 Jun;42(6):408-13. doi: 10.1111/j.1440-1827.1992.tb03245.x. Acta Pathol Jpn. 1992. PMID: 1502901

10

Amyloid beta-protein ending at Thr43 is a minor component of some diffuse plaques in the Alzheimer's disease brain, but is not found in cerebrovascular amyloid.

Iizuka T, Shoji M, Harigaya Y, Kawarabayashi T, Watanabe M, Kanai M, Hirai S. Iizuka T, et al. Among authors: watanabe m. Brain Res. 1995 Dec 8;702(1-2):275-8. doi: 10.1016/0006-8993(95)01163-2. Brain Res. 1995. PMID: 8846089

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