Ishikawa A - Search Results

1

Co-localization of alpha-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration.

Piao YS, Hayashi S, Hasegawa M, Wakabayashi K, Yamada M, Yoshimoto M, Ishikawa A, Iwatsubo T, Takahashi H. Piao YS, et al. Among authors: ishikawa a. Acta Neuropathol. 2001 Mar;101(3):285-93. doi: 10.1007/s004010000292. Acta Neuropathol. 2001. PMID: 11307630

2

Multiple system atrophy with severe involvement of the motor cortical areas and cerebral white matter.

Wakabayashi K, Ikeuchi T, Ishikawa A, Takahashi H. Wakabayashi K, et al. Among authors: ishikawa a. J Neurol Sci. 1998;156(1):114-7. doi: 10.1016/s0022-510x(98)00018-5. J Neurol Sci. 1998. PMID: 9559999

3

Autosomal dominant diffuse Lewy body disease.

Wakabayashi K, Hayashi S, Ishikawa A, Hayashi T, Okuizumi K, Tanaka H, Tsuji S, Takahashi H. Wakabayashi K, et al. Among authors: ishikawa a. Acta Neuropathol. 1998 Aug;96(2):207-10. doi: 10.1007/s004010050883. Acta Neuropathol. 1998. PMID: 9705138

4

Apolipoprotein E epsilon4 allele and progression of cortical Lewy body pathology in Parkinson's disease.

Wakabayashi K, Kakita A, Hayashi S, Okuizumi K, Onodera O, Tanaka H, Ishikawa A, Tsuji S, Takahashi H. Wakabayashi K, et al. Among authors: ishikawa a. Acta Neuropathol. 1998 May;95(5):450-4. doi: 10.1007/s004010050824. Acta Neuropathol. 1998. PMID: 9600590

5

An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.

Hayashi S, Wakabayashi K, Ishikawa A, Nagai H, Saito M, Maruyama M, Takahashi T, Ozawa T, Tsuji S, Takahashi H. Hayashi S, et al. Among authors: ishikawa a. Mov Disord. 2000 Sep;15(5):884-8. doi: 10.1002/1531-8257(200009)15:5<884::aid-mds1019>3.0.co;2-8. Mov Disord. 2000. PMID: 11009195

6

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: ishikawa a. Arch Neurol. 2008 Apr;65(4):514-9. doi: 10.1001/archneur.65.4.514. Arch Neurol. 2008. PMID: 18413475

7

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. Ann Neurol. 2005 Mar;57(3):429-34. doi: 10.1002/ana.20393. Ann Neurol. 2005. PMID: 15732120

8

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: ishikawa a. J Neurosci. 2007 Nov 28;27(48):13092-7. doi: 10.1523/JNEUROSCI.4244-07.2007. J Neurosci. 2007. PMID: 18045903 Free PMC article.

9

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.

Maruyama M, Ikeuchi T, Saito M, Ishikawa A, Yuasa T, Tanaka H, Hayashi S, Wakabayashi K, Takahashi H, Tsuji S. Maruyama M, et al. Among authors: ishikawa a. Ann Neurol. 2000 Aug;48(2):245-50. Ann Neurol. 2000. PMID: 10939576

10

Cardiac sympathetic denervation in Parkinson's disease linked to SNCA duplication.

Orimo S, Uchihara T, Nakamura A, Mori F, Ikeuchi T, Onodera O, Nishizawa M, Ishikawa A, Kakita A, Wakabayashi K, Takahashi H. Orimo S, et al. Among authors: ishikawa a. Acta Neuropathol. 2008 Nov;116(5):575-7. doi: 10.1007/s00401-008-0428-5. Epub 2008 Aug 28. Acta Neuropathol. 2008. PMID: 18751989 No abstract available.

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