Onodera O - Search Results

1

Novel partial deletions, frameshift and missense mutations of CSF1R in patents with CSF1R-related leukoencephalopathy.

Ishiguro T, Konno T, Hara N, Zhu B, Okada S, Shibata M, Saika R, Kitano T, Toko M, Nezu T, Hama Y, Kawazoe T, Takahashi-Iwata I, Yabe I, Sato K, Takeda H, Toda S, Nishimiya J, Teduka T, Nozaki H, Kasuga K, Miyashita A, Onodera O, Ikeuchi T. Ishiguro T, et al. Among authors: onodera o. Eur J Neurol. 2023 Jul;30(7):1861-1870. doi: 10.1111/ene.15796. Epub 2023 Mar 30. Eur J Neurol. 2023. PMID: 36943150

2

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.

Onodera O, Oyake M, Takano H, Ikeuchi T, Igarashi S, Tsuji S. Onodera O, et al. Am J Hum Genet. 1995 Nov;57(5):1050-60. Am J Hum Genet. 1995. PMID: 7485154 Free PMC article.

3

Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.

Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S. Ikeuchi T, et al. Among authors: onodera o. Clin Neurosci. 1995;3(1):23-7. Clin Neurosci. 1995. PMID: 7614090

4

Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipation.

Ikeuchi T, Onodera O, Oyake M, Koide R, Tanaka H, Tsuji S. Ikeuchi T, et al. Among authors: onodera o. Semin Cell Biol. 1995 Feb;6(1):37-44. doi: 10.1016/1043-4682(95)90013-6. Semin Cell Biol. 1995. PMID: 7620120 Review.

5

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: onodera o. Ann Neurol. 1995 Jun;37(6):769-75. doi: 10.1002/ana.410370610. Ann Neurol. 1995. PMID: 7778850

6

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: onodera o. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

7

No mutation in the entire coding region of the alpha-synuclein gene in pathologically confirmed cases of multiple system atrophy.

Ozawa T, Takano H, Onodera O, Kobayashi H, Ikeuchi T, Koide R, Okuizumi K, Shimohata T, Wakabayashi K, Takahashi H, Tsuji S. Ozawa T, et al. Among authors: onodera o. Neurosci Lett. 1999 Jul 30;270(2):110-2. doi: 10.1016/s0304-3940(99)00475-9. Neurosci Lett. 1999. PMID: 10462110

8

Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5.

Ohtake H, Shimohata T, Terajima K, Kimura T, Jo R, Kaseda R, Iizuka O, Takano M, Akaiwa Y, Goto H, Kobayashi H, Sugai T, Muratake T, Hosoki T, Shioiri T, Okamoto K, Onodera O, Tanaka K, Someya T, Nakada T, Tsuji S. Ohtake H, et al. Among authors: onodera o. Neurology. 2004 May 11;62(9):1601-3. doi: 10.1212/01.wnl.0000123117.11264.0e. Neurology. 2004. PMID: 15136690

9

[A late-onset case of oculopharyngeal muscular dystrophy carrying a (GCG)8 repeat expansion in the PAPBN1 gene].

Tokutake T, Ikeuchi T, Tanaka K, Onodera O, Nishizawa M. Tokutake T, et al. Among authors: onodera o. Rinsho Shinkeigaku. 2005 Jun;45(6):437-40. Rinsho Shinkeigaku. 2005. PMID: 16022469 Japanese.

10

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: onodera o. Mov Disord. 2007 Apr 30;22(6):857-62. doi: 10.1002/mds.21443. Mov Disord. 2007. PMID: 17357132

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