Goto J - Search Results

1

Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of DHH.

Sato NS, Maekawa R, Ishiura H, Mitsui J, Naruse H, Tokushige SI, Sugie K, Tate G, Shimizu J, Goto J, Tsuji S, Shiio Y. Sato NS, et al. Among authors: goto j. Ann Clin Transl Neurol. 2017 May 22;4(6):415-421. doi: 10.1002/acn3.417. eCollection 2017 Jun. Ann Clin Transl Neurol. 2017. PMID: 28589169 Free PMC article.

2

Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease.

Maeda MH, Mitsui J, Soong BW, Takahashi Y, Ishiura H, Hayashi S, Shirota Y, Ichikawa Y, Matsumoto H, Arai M, Okamoto T, Miyama S, Shimizu J, Inazawa J, Goto J, Tsuji S. Maeda MH, et al. Among authors: goto j. Ann Neurol. 2012 Jan;71(1):84-92. doi: 10.1002/ana.22658. Ann Neurol. 2012. PMID: 22275255

3

[Therapeutic trial design issues for future disease-modifying therapy of multiple system atrophy].

Ichikawa Y, Goto J, Nakahara Y, Mitsui J, Tsuji S. Ichikawa Y, et al. Among authors: goto j. Rinsho Shinkeigaku. 2011 Nov;51(11):910-3. doi: 10.5692/clinicalneurol.51.910. Rinsho Shinkeigaku. 2011. PMID: 22277413 Japanese.

4

Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology.

Ikenaga C, Kubota A, Kadoya M, Taira K, Uchio N, Hida A, Maeda MH, Nagashima Y, Ishiura H, Kaida K, Goto J, Tsuji S, Shimizu J. Ikenaga C, et al. Among authors: goto j. Neurology. 2017 Sep 5;89(10):1060-1068. doi: 10.1212/WNL.0000000000004333. Epub 2017 Aug 9. Neurology. 2017. PMID: 28794251

5

Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis.

Ikenaga C, Date H, Kanagawa M, Mitsui J, Ishiura H, Yoshimura J, Pinal-Fernandez I, Mammen AL, Lloyd TE, Tsuji S, Shimizu J, Toda T, Goto J. Ikenaga C, et al. Among authors: goto j. Ann Neurol. 2022 Mar;91(3):317-328. doi: 10.1002/ana.26304. Epub 2022 Feb 11. Ann Neurol. 2022. PMID: 35064929 Free PMC article.

6

Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.

Takahashi Y, Seki N, Ishiura H, Mitsui J, Matsukawa T, Kishino A, Onodera O, Aoki M, Shimozawa N, Murayama S, Itoyama Y, Suzuki Y, Sobue G, Nishizawa M, Goto J, Tsuji S. Takahashi Y, et al. Among authors: goto j. Arch Neurol. 2008 Oct;65(10):1326-32. doi: 10.1001/archneur.65.10.1326. Arch Neurol. 2008. PMID: 18852346

7

[Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease].

Hashimoto M, Shimizu J, Shirota Y, Momose Y, Goto J, Takeda K, Tsuji S. Hashimoto M, et al. Among authors: goto j. Rinsho Shinkeigaku. 2009 Feb-Mar;49(2-3):109-14. doi: 10.5692/clinicalneurol.49.109. Rinsho Shinkeigaku. 2009. PMID: 19348176 Japanese.

8

Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1.

Ishiura H, Fukuda Y, Mitsui J, Nakahara Y, Ahsan B, Takahashi Y, Ichikawa Y, Goto J, Sakai T, Tsuji S. Ishiura H, et al. Among authors: goto j. Neurogenetics. 2011 May;12(2):117-21. doi: 10.1007/s10048-010-0271-4. Epub 2011 Jan 26. Neurogenetics. 2011. PMID: 21267618

9

C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan.

Ishiura H, Takahashi Y, Mitsui J, Yoshida S, Kihira T, Kokubo Y, Kuzuhara S, Ranum LP, Tamaoki T, Ichikawa Y, Date H, Goto J, Tsuji S. Ishiura H, et al. Among authors: goto j. Arch Neurol. 2012 Sep;69(9):1154-8. doi: 10.1001/archneurol.2012.1219. Arch Neurol. 2012. PMID: 22637429

10

Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population.

Naruse H, Takahashi Y, Kihira T, Yoshida S, Kokubo Y, Kuzuhara S, Ishiura H, Amagasa M, Murayama S, Tsuji S, Goto J. Naruse H, et al. Among authors: goto j. Amyotroph Lateral Scler. 2012 Oct;13(6):562-6. doi: 10.3109/17482968.2012.684213. Epub 2012 Jun 18. Amyotroph Lateral Scler. 2012. PMID: 22708870

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