Ishikawa A - Search Results

1

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Igarashi S, Tanno Y, Onodera O, Yamazaki M, Sato S, Ishikawa A, Miyatani N, Nagashima M, Ishikawa Y, Sahashi K, et al. Igarashi S, et al. Among authors: ishikawa a, ishikawa y. Neurology. 1992 Dec;42(12):2300-2. doi: 10.1212/wnl.42.12.2300. Neurology. 1992. PMID: 1461383

2

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T, et al. Ikeuchi T, et al. Among authors: ishikawa a. Ann Neurol. 1995 Jun;37(6):769-75. doi: 10.1002/ana.410370610. Ann Neurol. 1995. PMID: 7778850

3

Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Koide R, Onodera O, Ikeuchi T, Kondo R, Tanaka H, Tokiguchi S, Tomoda A, Miike T, Isa F, Beppu H, Shimizu N, Watanabe Y, Horikawa Y, Shimohata T, Hirota K, Ishikawa A, Tsuji S. Koide R, et al. Among authors: ishikawa a. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

4

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, et al. Koide R, et al. Among authors: ishikawa a. Nat Genet. 1994 Jan;6(1):9-13. doi: 10.1038/ng0194-9. Nat Genet. 1994. PMID: 8136840

5

[An autopsied case of manifesting chorea, serum antibody to brain proteins, neuronal degeneration in striatum and grumose degeneration in dentate nucleus].

Ishikawa A, Miyatani N, Yuasa T, Tanaka K, Oyanagi K. Ishikawa A, et al. Rinsho Shinkeigaku. 1990 May;30(5):510-5. Rinsho Shinkeigaku. 1990. PMID: 2144802 Japanese.

6

[A case report of late-onset Huntington disease without family history and caudate atrophy who has diagnosed clinicopathologically and genetically].

Saito M, Ishikawa A, Iwanaga K, Igarashi S, Takahashi H, Tsuji S. Saito M, et al. Among authors: ishikawa a. No To Shinkei. 1996 Oct;48(10):949-53. No To Shinkei. 1996. PMID: 8921535 Japanese.

7

Beta-synuclein gene alterations in dementia with Lewy bodies.

Ohtake H, Limprasert P, Fan Y, Onodera O, Kakita A, Takahashi H, Bonner LT, Tsuang DW, Murray IV, Lee VM, Trojanowski JQ, Ishikawa A, Idezuka J, Murata M, Toda T, Bird TD, Leverenz JB, Tsuji S, La Spada AR. Ohtake H, et al. Among authors: ishikawa a. Neurology. 2004 Sep 14;63(5):805-11. doi: 10.1212/01.wnl.0000139870.14385.3c. Neurology. 2004. PMID: 15365127 Free PMC article.

8

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

9

A non-familial Huntington's disease patient with grumose degeneration in the dentate nucleus.

Ishikawa A, Oyanagi K, Tanaka K, Igarashi S, Sato T, Tsuji S. Ishikawa A, et al. Acta Neurol Scand. 1999 May;99(5):322-6. doi: 10.1111/j.1600-0404.1999.tb00684.x. Acta Neurol Scand. 1999. PMID: 10348164

10

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

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