Miyamoto R - Search Results

1

Hung-up Knee Jerk in Huntington's Disease.

Fukumoto T, Miyamoto R. Fukumoto T, et al. Among authors: miyamoto r. N Engl J Med. 2020 Feb 13;382(7):e10. doi: 10.1056/NEJMicm1910309. N Engl J Med. 2020. PMID: 32053302 No abstract available.

2

Reversible mixed perfusion on ¹²³I-IMP SPECT in anti-AMPA receptor encephalitis: A case report.

Fukumoto T, Miyamoto R, Fujita K, Murakami N, Matsui N, Izumi Y. Fukumoto T, et al. Among authors: miyamoto r. J Neurol Sci. 2021 Feb 15;421:117306. doi: 10.1016/j.jns.2020.117306. Epub 2021 Jan 4. J Neurol Sci. 2021. PMID: 33450618 No abstract available.

3

A novel COL4A1 variant associated with recurrent epistaxis and glioblastoma.

Muto K, Miyamoto R, Terasawa Y, Shimatani Y, Hara K, Kakimoto T, Fukumoto T, Osaki Y, Fujita K, Harada M, Uehara H, Takagi Y, Izumi Y. Muto K, et al. Among authors: miyamoto r. Hum Genome Var. 2021 May 14;8(1):18. doi: 10.1038/s41439-021-00150-0. Hum Genome Var. 2021. PMID: 33990551 Free PMC article.

4

"Burnt-out" progressive multifocal leukoencephalopathy in idiopathic CD4⁺ lymphocytopenia.

Fukumoto T, Sakashita Y, Katada F, Takeuchi R, Miyamoto R, Izumi Y, Sato S, Shibayama H, Takahashi K, Suzuki T, Nakamichi K, Murayama S, Fukutake T. Fukumoto T, et al. Among authors: miyamoto r. Neuropathology. 2021 Dec;41(6):484-488. doi: 10.1111/neup.12773. Epub 2021 Sep 30. Neuropathology. 2021. PMID: 34595780

5

[Clinical features of tetanus: a review with case reports].

Fukutake T, Miyamoto R. Fukutake T, et al. Among authors: miyamoto r. Brain Nerve. 2011 Oct;63(10):1101-10. Brain Nerve. 2011. PMID: 21987566 Review. Japanese.

6

Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease.

Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H. Izumi Y, et al. Among authors: miyamoto r. Neurology. 2013 Feb 5;80(6):600-1. doi: 10.1212/WNL.0b013e3182815529. Epub 2013 Jan 16. Neurology. 2013. PMID: 23325900 No abstract available.

7

Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia.

Maruyama H, Morino H, Miyamoto R, Murakami N, Hamano T, Kawakami H. Maruyama H, et al. Among authors: miyamoto r. Clin Genet. 2014 Mar;85(3):296-7. doi: 10.1111/cge.12140. Epub 2013 Apr 4. Clin Genet. 2014. PMID: 23551081 No abstract available.

8

[Dystonia genes and elucidation of their roles in dystonia pathogenesis].

Kawarai T, Miyamoto R, Murakami N, Miyazaki Y, Koizumi H, Sako W, Mukai Y, Sato K, Matsumoto S, Sakamoto T, Izumi Y, Kaji R. Kawarai T, et al. Among authors: miyamoto r. Rinsho Shinkeigaku. 2013;53(6):419-29. doi: 10.5692/clinicalneurol.53.419. Rinsho Shinkeigaku. 2013. PMID: 23782819 Review. Japanese.

9

Lack of C9orf72 expansion in 406 sporadic and familial cases of idiopathic dystonia in Japan.

Miyamoto R, Kawarai T, Oki R, Matsumoto S, Izumi Y, Kaji R. Miyamoto R, et al. Mov Disord. 2015 Sep;30(10):1430-1. doi: 10.1002/mds.26310. Epub 2015 Jul 14. Mov Disord. 2015. PMID: 26173439 No abstract available.

10

Autopsy case of severe generalized dystonia and static ataxia with marked cerebellar atrophy.

Miyamoto R, Sumikura H, Takeuchi T, Sanada M, Fujita K, Kawarai T, Mure H, Morigaki R, Goto S, Murayama S, Izumi Y, Kaji R. Miyamoto R, et al. Neurology. 2015 Oct 27;85(17):1522-4. doi: 10.1212/WNL.0000000000002061. Epub 2015 Sep 25. Neurology. 2015. PMID: 26408497 No abstract available.

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