Mizuta I - Search Results

1

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.

Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M; Alexander Disease Study Group in Japan. Yoshida T, et al. Among authors: mizuta i. J Neurol. 2011 Nov;258(11):1998-2008. doi: 10.1007/s00415-011-6056-3. Epub 2011 May 1. J Neurol. 2011. PMID: 21533827

2

Mutations for Gaucher disease confer high susceptibility to Parkinson disease.

Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S. Mitsui J, et al. Among authors: mizuta i. Arch Neurol. 2009 May;66(5):571-6. doi: 10.1001/archneurol.2009.72. Arch Neurol. 2009. PMID: 19433656

3

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.

Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M. Yoshida T, et al. Among authors: mizuta i. Acta Neurol Scand. 2011 Aug;124(2):104-8. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849398

4

Serial MRI changes in a patient with infantile Alexander disease and prolonged survival.

Shiihara T, Yoneda T, Mizuta I, Yoshida T, Nakagawa M, Shimizu N. Shiihara T, et al. Among authors: mizuta i. Brain Dev. 2011 Aug;33(7):604-7. doi: 10.1016/j.braindev.2010.10.007. Epub 2010 Oct 30. Brain Dev. 2011. PMID: 21041050

5

A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease.

Shiga K, Noto Y, Mizuta I, Hashiguchi A, Takashima H, Nakagawa M. Shiga K, et al. Among authors: mizuta i. J Peripher Nerv Syst. 2012 Jun;17(2):206-9. doi: 10.1111/j.1529-8027.2012.00403.x. J Peripher Nerv Syst. 2012. PMID: 22734907

6

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease.

Yoshida T, Mizuta I, Saito K, Ohara R, Kurisaki H, Ohnari K, Riku Y, Hayashi Y, Suzuki H, Shii H, Fujiwara Y, Yonezu T, Nagaishi A, Nakagawa M. Yoshida T, et al. Among authors: mizuta i. J Hum Genet. 2013 Sep;58(9):635-8. doi: 10.1038/jhg.2013.83. Epub 2013 Aug 1. J Hum Genet. 2013. PMID: 23903069

7

Definite familial multiple system atrophy with unknown genetics.

Itoh K, Kasai T, Tsuji Y, Saito K, Mizuta I, Harada Y, Sudoh S, Mizuno T, Nakagawa M, Fushiki S. Itoh K, et al. Among authors: mizuta i. Neuropathology. 2014 Jun;34(3):309-13. doi: 10.1111/neup.12092. Epub 2014 Jan 7. Neuropathology. 2014. PMID: 24397755

8

Identification of ter94, Drosophila VCP, as a strong modulator of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS.

Azuma Y, Tokuda T, Shimamura M, Kyotani A, Sasayama H, Yoshida T, Mizuta I, Mizuno T, Nakagawa M, Fujikake N, Ueyama M, Nagai Y, Yamaguchi M. Azuma Y, et al. Among authors: mizuta i. Hum Mol Genet. 2014 Jul 1;23(13):3467-80. doi: 10.1093/hmg/ddu055. Epub 2014 Feb 4. Hum Mol Genet. 2014. PMID: 24497576

9

Genetic link between Cabeza, a Drosophila homologue of Fused in Sarcoma (FUS), and the EGFR signaling pathway.

Shimamura M, Kyotani A, Azuma Y, Yoshida H, Binh Nguyen T, Mizuta I, Yoshida T, Mizuno T, Nakagawa M, Tokuda T, Yamaguchi M. Shimamura M, et al. Among authors: mizuta i. Exp Cell Res. 2014 Aug 1;326(1):36-45. doi: 10.1016/j.yexcr.2014.06.004. Epub 2014 Jun 11. Exp Cell Res. 2014. PMID: 24928275

10

Hereditary diffuse leukoencephalopathy with spheroids characterized by spastic hemiplegia preceding mental impairment.

Kitani-Morii F, Kasai T, Tomonaga K, Saito K, Mizuta I, Yoshioka A, Nakagawa M, Mizuno T. Kitani-Morii F, et al. Among authors: mizuta i. Intern Med. 2014;53(12):1377-80. doi: 10.2169/internalmedicine.53.1932. Epub 2014 Jun 15. Intern Med. 2014. PMID: 24930661 Free article.

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