Shoji M - Search Results

1

Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls.

Shizuka M, Watanabe M, Ikeda Y, Mizushima K, Okamoto K, Shoji M. Shizuka M, et al. Among authors: shoji m. J Neurol Sci. 1998 Nov 26;161(1):85-7. doi: 10.1016/s0022-510x(98)00270-6. J Neurol Sci. 1998. PMID: 9879686

2

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: shoji 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

3

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: shoji 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

4

[Mutation analysis of the CACNL1A3 gene in Japanese hypokalemic periodic paralysis families].

Ikeda Y, Watanabe M, Shoji M. Ikeda Y, et al. Among authors: shoji m. Nihon Rinsho. 1997 Dec;55(12):3247-52. Nihon Rinsho. 1997. PMID: 9436445 Review. Japanese.

5

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: shoji 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

6

Combination assay of CSF tau, A beta 1-40 and A beta 1-42(43) as a biochemical marker of Alzheimer's disease.

Shoji M, Matsubara E, Kanai M, Watanabe M, Nakamura T, Tomidokoro Y, Shizuka M, Wakabayashi K, Igeta Y, Ikeda Y, Mizushima K, Amari M, Ishiguro K, Kawarabayashi T, Harigaya Y, Okamoto K, Hirai S. Shoji M, et al. J Neurol Sci. 1998 Jun 30;158(2):134-40. doi: 10.1016/s0022-510x(98)00122-1. J Neurol Sci. 1998. PMID: 9702683

7

Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, gamma-globulin, and alpha-fetoprotein.

Watanabe M, Sugai Y, Concannon P, Koenig M, Schmitt M, Sato M, Shizuka M, Mizushima K, Ikeda Y, Tomidokoro Y, Okamoto K, Shoji M. Watanabe M, et al. Among authors: shoji m. Ann Neurol. 1998 Aug;44(2):265-9. doi: 10.1002/ana.410440220. Ann Neurol. 1998. PMID: 9708552

8

Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.

Mizushima K, Watanabe M, Kondo I, Okamoto K, Shizuka M, Abe K, Aoki M, Shoji M. Mizushima K, et al. Among authors: shoji m. J Med Genet. 1999 Feb;36(2):112-4. J Med Genet. 1999. PMID: 10051008 Free PMC article.

9

Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan.

Ikeda Y, Shizuka M, Watanabe M, Okamoto K, Shoji M. Ikeda Y, et al. Among authors: shoji m. Neurology. 2000 Feb 22;54(4):950-5. doi: 10.1212/wnl.54.4.950. Neurology. 2000. PMID: 10690991

10

Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI.

Ikeda Y, Shizuka-Ikeda M, Watanabe M, Schmitt M, Okamoto K, Shoji M. Ikeda Y, et al. Among authors: shoji m. J Neurol Sci. 2000 Dec 15;182(1):76-9. doi: 10.1016/s0022-510x(00)00446-9. J Neurol Sci. 2000. PMID: 11102643

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