Nishizawa M - Search Results

1

Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.

Kaneko H, Kakita A, Kasuga K, Nozaki H, Ishikawa A, Miyashita A, Kuwano R, Ito G, Iwatsubo T, Takahashi H, Nishizawa M, Onodera O, Sisodia SS, Ikeuchi T. Kaneko H, et al. Among authors: nishizawa m. J Neurosci. 2007 Nov 28;27(48):13092-7. doi: 10.1523/JNEUROSCI.4244-07.2007. J Neurosci. 2007. PMID: 18045903 Free PMC article.

2

A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.

Ishikawa A, Piao YS, Miyashita A, Kuwano R, Onodera O, Ohtake H, Suzuki M, Nishizawa M, Takahashi H. Ishikawa A, et al. Among authors: nishizawa m. Ann Neurol. 2005 Mar;57(3):429-34. doi: 10.1002/ana.20393. Ann Neurol. 2005. PMID: 15732120

3

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

Ikeuchi T, Kakita A, Shiga A, Kasuga K, Kaneko H, Tan CF, Idezuka J, Wakabayashi K, Onodera O, Iwatsubo T, Nishizawa M, Takahashi H, Ishikawa A. Ikeuchi T, et al. Among authors: nishizawa m. Arch Neurol. 2008 Apr;65(4):514-9. doi: 10.1001/archneur.65.4.514. Arch Neurol. 2008. PMID: 18413475

4

Generation of intracellular domain of insulin receptor tyrosine kinase by gamma-secretase.

Kasuga K, Kaneko H, Nishizawa M, Onodera O, Ikeuchi T. Kasuga K, et al. Among authors: nishizawa m. Biochem Biophys Res Commun. 2007 Aug 17;360(1):90-6. doi: 10.1016/j.bbrc.2007.06.022. Epub 2007 Jun 12. Biochem Biophys Res Commun. 2007. PMID: 17577576

5

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease.

Kasuga K, Shimohata T, Nishimura A, Shiga A, Mizuguchi T, Tokunaga J, Ohno T, Miyashita A, Kuwano R, Matsumoto N, Onodera O, Nishizawa M, Ikeuchi T. Kasuga K, et al. Among authors: nishizawa m. J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):1050-2. doi: 10.1136/jnnp.2008.161703. J Neurol Neurosurg Psychiatry. 2009. PMID: 19684239

6

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O. Nozaki H, et al. Among authors: nishizawa m. Mov Disord. 2007 Apr 30;22(6):857-62. doi: 10.1002/mds.21443. Mov Disord. 2007. PMID: 17357132

7

[Hereditary spastic paraplegia associated with thin corpus callosum].

Kasuga K, Nishizawa M. Kasuga K, et al. Among authors: nishizawa m. No To Shinkei. 2003 Sep;55(9):765-70. No To Shinkei. 2003. PMID: 14571838 Review. Japanese. No abstract available.

8

Selective silencing of a mutant transthyretin allele by small interfering RNAs.

Kurosawa T, Igarashi S, Nishizawa M, Onodera O. Kurosawa T, et al. Among authors: nishizawa m. Biochem Biophys Res Commun. 2005 Nov 25;337(3):1012-8. doi: 10.1016/j.bbrc.2005.09.142. Epub 2005 Oct 3. Biochem Biophys Res Commun. 2005. PMID: 16225852

9

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, Tsujino A, Nishizawa M, Kakita A, Takahashi H. Tan CF, et al. Among authors: nishizawa m. Acta Neuropathol. 2007 May;113(5):535-42. doi: 10.1007/s00401-007-0206-9. Epub 2007 Feb 27. Acta Neuropathol. 2007. PMID: 17333220

10

Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?

Tan CF, Piao YS, Kakita A, Yamada M, Takano H, Tanaka M, Mano A, Makino K, Nishizawa M, Wakabayashi K, Takahashi H. Tan CF, et al. Among authors: nishizawa m. Acta Neuropathol. 2005 Mar;109(3):329-38. doi: 10.1007/s00401-004-0933-0. Epub 2004 Nov 12. Acta Neuropathol. 2005. PMID: 15841415

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