Ishiura H - Search Results

1

[Recommendations (Proposal) for promoting research for overcoming neurological diseases 2020].

Mochizuki H, Aoki M, Ikenaka K, Inoue H, Iwatsubo T, Ugawa Y, Okazawa H, Ono K, Onodera O, Kitagawa K, Saito Y, Shimohata T, Takahashi R, Toda T, Nakahara J, Matsumoto R, Mizusawa H, Mitsui J, Murayama S, Katsuno M; Future Vision Committee of Japanese Society of Neurology; Aoki Y, Ishiura H, Izumi Y, Koike H, Shimada H, Takahashi Y, Tokuda T, Nakajima H, Hatano T, Misawa S, Watanabe H. Mochizuki H, et al. Among authors: ishiura h. Rinsho Shinkeigaku. 2022 Jun 24;62(6):443-457. doi: 10.5692/clinicalneurol.cn-001696. Epub 2022 May 28. Rinsho Shinkeigaku. 2022. PMID: 35644580 Japanese.

2

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: ishiura h. Arch Neurol. 2008 Oct;65(10):1326-32. doi: 10.1001/archneur.65.10.1326. Arch Neurol. 2008. PMID: 18852346

3

[A case of autosomal recessive hypomyelinating leukodystrophy without GJA12 mutation presenting a novel phenotype].

Ishikawa T, Sato K, Shimazaki R, Goto K, Matsuda T, Ishiura H. Ishikawa T, et al. Among authors: ishiura h. Rinsho Shinkeigaku. 2010 Jan;50(1):7-11. doi: 10.5692/clinicalneurol.50.7. Rinsho Shinkeigaku. 2010. PMID: 20120347 Japanese.

4

Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer.

Mitsui J, Fukuda Y, Azuma K, Tozaki H, Ishiura H, Takahashi Y, Goto J, Tsuji S. Mitsui J, et al. Among authors: ishiura h. J Hum Genet. 2010 Jul;55(7):448-55. doi: 10.1038/jhg.2010.46. Epub 2010 May 20. J Hum Genet. 2010. PMID: 20485446

5

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. Neurogenetics. 2011 May;12(2):117-21. doi: 10.1007/s10048-010-0271-4. Epub 2011 Jan 26. Neurogenetics. 2011. PMID: 21267618

6

[Japan spastic paraplegia research consortium (JASPAC)].

Takiyama Y, Ishiura H, Shimazaki H, Namekawa M, Takahashi Y, Goto J, Tsuji S, Nishizawa M. Takiyama Y, et al. Among authors: ishiura h. Rinsho Shinkeigaku. 2010 Nov;50(11):931-4. doi: 10.5692/clinicalneurol.50.931. Rinsho Shinkeigaku. 2010. PMID: 21921516 Japanese.

7

[Massively parallel sequence analysis for revealing causes of neuromuscular disorders].

Ishiura H, Tsuji S. Ishiura H, et al. Rinsho Shinkeigaku. 2010 Nov;50(11):957-8. doi: 10.5692/clinicalneurol.50.957. Rinsho Shinkeigaku. 2010. PMID: 21921526 Japanese.

8

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: ishiura h. Ann Neurol. 2012 Jan;71(1):84-92. doi: 10.1002/ana.22658. Ann Neurol. 2012. PMID: 22275255

9

Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type.

Taira M, Ishiura H, Mitsui J, Takahashi Y, Hayashi T, Shimizu J, Matsukawa T, Saito N, Okada K, Tsuji S, Sawamura H, Amano S, Goto J, Tsuji S. Taira M, et al. Among authors: ishiura h. Neurogenetics. 2012 Aug;13(3):237-43. doi: 10.1007/s10048-012-0330-0. Epub 2012 May 24. Neurogenetics. 2012. PMID: 22622774

10

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. Arch Neurol. 2012 Sep;69(9):1154-8. doi: 10.1001/archneurol.2012.1219. Arch Neurol. 2012. PMID: 22637429

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