Honma Y - Search Results

1

A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis.

Nakano R, Sato S, Inuzuka T, Sakimura K, Mishina M, Takahashi H, Ikuta F, Honma Y, Fujii J, Taniguchi N, et al. Nakano R, et al. Among authors: honma y. Biochem Biophys Res Commun. 1994 Apr 29;200(2):695-703. doi: 10.1006/bbrc.1994.1506. Biochem Biophys Res Commun. 1994. PMID: 8179602

2

Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene.

Takahashi H, Makifuchi T, Nakano R, Sato S, Inuzuka T, Sakimura K, Mishina M, Honma Y, Tsuji S, Ikuta F. Takahashi H, et al. Among authors: honma y. Acta Neuropathol. 1994;88(2):185-8. doi: 10.1007/BF00294513. Acta Neuropathol. 1994. PMID: 7985500

3

Amyotrophic lateral sclerosis: occurrence of Bunina bodies in the locus ceruleus pigmented neurons.

Iwanaga K, Wakabayashi K, Honma Y, Takahashi H. Iwanaga K, et al. Among authors: honma y. Clin Neuropathol. 1997 Jan-Feb;16(1):23-6. Clin Neuropathol. 1997. PMID: 9020390

4

[An autopsy case of thrombotic thrombocytopenic purpura--topography of the vascular lesion in the central nervous system].

Yamada M, Yoshida Y, Ikuta F, Honma Y. Yamada M, et al. Among authors: honma y. No To Shinkei. 1989 Apr;41(4):391-6. No To Shinkei. 1989. PMID: 2765302 Japanese.

5

Autosomal dominant cerebellar ataxia (SCA6): clinical, genetic and neuropathological study in a family.

Takahashi H, Ikeuchi T, Honma Y, Hayashi S, Tsuji S. Takahashi H, et al. Among authors: honma y. Acta Neuropathol. 1998 Apr;95(4):333-7. doi: 10.1007/s004010050807. Acta Neuropathol. 1998. PMID: 9560009

6

Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.

Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S. Ikeuchi T, et al. Among authors: honma y. Ann Neurol. 1997 Dec;42(6):879-84. doi: 10.1002/ana.410420609. Ann Neurol. 1997. PMID: 9403480

7

Novel CHP1 mutation in autosomal-recessive cerebellar ataxia: autopsy features of two siblings.

Saito R, Hara N, Tada M, Honma Y, Miyashita A, Onodera O, Ikeuchi T, Kakita A. Saito R, et al. Among authors: honma y. Acta Neuropathol Commun. 2020 Aug 12;8(1):134. doi: 10.1186/s40478-020-01008-2. Acta Neuropathol Commun. 2020. PMID: 32787936 Free PMC article. No abstract available.

8

[Gene diagnosis of patients with chorea].

Shimohata T, Onodera O, Honma Y, Hirota K, Nunomura Y, Kimura T, Kawachi I, Sanpei K, Nishizawa M, Tsuji S. Shimohata T, et al. Among authors: honma y. Rinsho Shinkeigaku. 2004 Mar;44(3):149-53. Rinsho Shinkeigaku. 2004. PMID: 15233265 Japanese.

9

An autopsy case of dementia with Lewy bodies showing autonomic failure and dementia as the initial symptoms.

Kanazawa M, Sanpei K, Toyoshima Y, Kawachi I, Honma Y, Takahashi H. Kanazawa M, et al. Among authors: honma y. Mov Disord. 2007 Jun 15;22(8):1212-3. doi: 10.1002/mds.21523. Mov Disord. 2007. PMID: 17486594 No abstract available.

10

Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.

Shimohata T, Hara K, Sanpei K, Nunomura J, Maeda T, Kawachi I, Kanazawa M, Kasuga K, Miyashita A, Kuwano R, Hirota K, Tsuji S, Onodera O, Nishizawa M, Honma Y. Shimohata T, et al. Among authors: honma y. Brain. 2007 Sep;130(Pt 9):2302-9. doi: 10.1093/brain/awm036. Epub 2007 Apr 2. Brain. 2007. PMID: 17405764

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