Matsuura E - Search Results

1

Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.

Higuchi Y, Ando M, Kojima F, Yuan J, Hashiguchi A, Yoshimura A, Hiramatsu Y, Nozuma S, Fukumura S, Yahikozawa H, Abe E, Toyoshima I, Sugawara M, Okamoto Y, Matsuura E, Takashima H. Higuchi Y, et al. Among authors: matsuura e. J Neurol. 2024 Jan;271(1):419-430. doi: 10.1007/s00415-023-11998-3. Epub 2023 Sep 26. J Neurol. 2024. PMID: 37750949 Free PMC article.

2

MRI studies of spinal visceral larva migrans syndrome.

Umehara F, Ookatsu H, Hayashi D, Uchida A, Douchi Y, Kawabata H, Goto R, Hashiguchi A, Matsuura E, Okubo R, Higuchi I, Arimura K, Nawa Y, Osame M. Umehara F, et al. Among authors: matsuura e. J Neurol Sci. 2006 Nov 1;249(1):7-12. doi: 10.1016/j.jns.2006.05.057. Epub 2006 Jul 3. J Neurol Sci. 2006. PMID: 16815465

3

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases.

Higuchi I, Hashiguchi A, Matsuura E, Higashi K, Shiraishi T, Hirata N, Arimura K, Osame M. Higuchi I, et al. Among authors: matsuura e. Neuromuscul Disord. 2007 Mar;17(3):221-6. doi: 10.1016/j.nmd.2006.11.008. Epub 2007 Feb 26. Neuromuscul Disord. 2007. PMID: 17324572

4

Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.

Yuan J, Higuchi Y, Nagado T, Nozuma S, Nakamura T, Matsuura E, Hashiguchi A, Sakiyama Y, Yoshimura A, Takashima H. Yuan J, et al. Among authors: matsuura e. J Peripher Nerv Syst. 2013 Mar;18(1):89-93. doi: 10.1111/jns5.12012. J Peripher Nerv Syst. 2013. PMID: 23521649

5

Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation.

Yuan J, Matsuura E, Higuchi Y, Hashiguchi A, Nakamura T, Nozuma S, Sakiyama Y, Yoshimura A, Izumo S, Takashima H. Yuan J, et al. Among authors: matsuura e. Neurology. 2013 Apr 30;80(18):1641-9. doi: 10.1212/WNL.0b013e3182904fdd. Epub 2013 Apr 17. Neurology. 2013. PMID: 23596073

6

Familial clusters of HTLV-1-associated myelopathy/tropical spastic paraparesis.

Nozuma S, Matsuura E, Matsuzaki T, Watanabe O, Kubota R, Izumo S, Takashima H. Nozuma S, et al. Among authors: matsuura e. PLoS One. 2014 May 6;9(5):e86144. doi: 10.1371/journal.pone.0086144. eCollection 2014. PLoS One. 2014. PMID: 24802839 Free PMC article.

7

Partial deficiency of emerin caused by a splice site mutation in EMD.

Yuan J, Ando M, Higuchi I, Sakiyama Y, Matsuura E, Michizono K, Watanabe O, Nagano S, Inamori Y, Hashiguchi A, Higuchi Y, Yoshimura A, Takashima H. Yuan J, et al. Among authors: matsuura e. Intern Med. 2014;53(14):1563-8. doi: 10.2169/internalmedicine.53.8922. Epub 2014 Jul 15. Intern Med. 2014. PMID: 25030574 Free article.

8

Visualization of HTLV-1-specific cytotoxic T lymphocytes in the spinal cords of patients with HTLV-1-associated myelopathy/tropical spastic paraparesis.

Matsuura E, Kubota R, Tanaka Y, Takashima H, Izumo S. Matsuura E, et al. J Neuropathol Exp Neurol. 2015 Jan;74(1):2-14. doi: 10.1097/NEN.0000000000000141. J Neuropathol Exp Neurol. 2015. PMID: 25470342 Free PMC article.

9

Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs.

Hashiguchi A, Higuchi Y, Nomura M, Nakamura T, Arata H, Yuan J, Yoshimura A, Okamoto Y, Matsuura E, Takashima H. Hashiguchi A, et al. Among authors: matsuura e. J Peripher Nerv Syst. 2014 Dec;19(4):311-6. doi: 10.1111/jns.12102. J Peripher Nerv Syst. 2014. PMID: 25583183

10

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP).

Matsuura E, Yoshimura A, Nozuma S, Higuchi I, Kubota R, Takashima H. Matsuura E, et al. BMC Neurol. 2015 Feb 28;15:18. doi: 10.1186/s12883-015-0275-7. BMC Neurol. 2015. PMID: 25884435 Free PMC article.

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