Nakamura H - Search Results

1

Systemic administration of the antisense oligonucleotide NS-065/NCNP-01 for skipping of exon 53 in patients with Duchenne muscular dystrophy.

Komaki H, Nagata T, Saito T, Masuda S, Takeshita E, Sasaki M, Tachimori H, Nakamura H, Aoki Y, Takeda S. Komaki H, et al. Among authors: nakamura h. Sci Transl Med. 2018 Apr 18;10(437):eaan0713. doi: 10.1126/scitranslmed.aan0713. Sci Transl Med. 2018. PMID: 29669851 Clinical Trial.

2

[Infrastructure for new drug development to treat muscular dystrophy: current status of patient registration (remudy)].

Nakamura H, Kimura E, Kawai M. Nakamura H, et al. Brain Nerve. 2011 Nov;63(11):1279-84. Brain Nerve. 2011. PMID: 22068481 Review. Japanese.

3

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

Nakamura H, Kimura E, Mori-Yoshimura M, Komaki H, Matsuda Y, Goto K, Hayashi YK, Nishino I, Takeda S, Kawai M. Nakamura H, et al. Orphanet J Rare Dis. 2013 Apr 19;8:60. doi: 10.1186/1750-1172-8-60. Orphanet J Rare Dis. 2013. PMID: 23601510 Free PMC article.

4

Prednisolone improves walking in Japanese Duchenne muscular dystrophy patients.

Takeuchi F, Yonemoto N, Nakamura H, Shimizu R, Komaki H, Mori-Yoshimura M, Hayashi YK, Nishino I, Kawai M, Kimura E, Takeda S. Takeuchi F, et al. Among authors: nakamura h. J Neurol. 2013 Dec;260(12):3023-9. doi: 10.1007/s00415-013-7104-y. Epub 2013 Sep 22. J Neurol. 2013. PMID: 24057148 Free PMC article.

5

Nationwide patient registry for GNE myopathy in Japan.

Mori-Yoshimura M, Hayashi YK, Yonemoto N, Nakamura H, Murata M, Takeda S, Nishino I, Kimura E. Mori-Yoshimura M, et al. Among authors: nakamura h. Orphanet J Rare Dis. 2014 Oct 11;9:150. doi: 10.1186/s13023-014-0150-4. Orphanet J Rare Dis. 2014. PMID: 25303967 Free PMC article.

6

[Infrastructure for the clinical research of muscular dystrophies: remudy and MDCTN].

Kimura E, Nakamura H, Mitsuhashi S, Takeuchi F, Mori-Yoshimura M, Shimizu R, Komaki H, Hayashi YK, Nishino I, Kawai M, Takeda S. Kimura E, et al. Among authors: nakamura h. Rinsho Shinkeigaku. 2014;54(12):1069-70. doi: 10.5692/clinicalneurol.54.1069. Rinsho Shinkeigaku. 2014. PMID: 25519964 Review. Japanese.

7

Trends in steroid therapy for Duchenne muscular dystrophy in Japan.

Takeuchi F, Komaki H, Nakamura H, Yonemoto N, Kashiwabara K, Kimura E, Takeda S. Takeuchi F, et al. Among authors: nakamura h. Muscle Nerve. 2016 Oct;54(4):673-80. doi: 10.1002/mus.25083. Epub 2016 Jul 14. Muscle Nerve. 2016. PMID: 26910583 Free PMC article.

8

Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network.

Shimizu R, Ogata K, Tamaura A, Kimura E, Ohata M, Takeshita E, Nakamura H, Takeda S, Komaki H. Shimizu R, et al. Among authors: nakamura h. BMC Health Serv Res. 2016 Jul 11;16:241. doi: 10.1186/s12913-016-1477-4. BMC Health Serv Res. 2016. PMID: 27401940 Free PMC article.

9

A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis.

Takeuchi F, Komaki H, Yamagata Z, Maruo K, Rodger S, Kirschner J, Kubota T, Kimura E, Takeda S, Gramsch K, Vry J, Bushby K, Lochmüller H, Wada K, Nakamura H. Takeuchi F, et al. Among authors: nakamura h. Neuromuscul Disord. 2017 Oct;27(10):894-904. doi: 10.1016/j.nmd.2017.06.557. Epub 2017 Jul 6. Neuromuscul Disord. 2017. PMID: 28807665 Free article.

10

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.

Okubo M, Goto K, Komaki H, Nakamura H, Mori-Yoshimura M, Hayashi YK, Mitsuhashi S, Noguchi S, Kimura E, Nishino I. Okubo M, et al. Among authors: nakamura h. Orphanet J Rare Dis. 2017 Aug 31;12(1):149. doi: 10.1186/s13023-017-0703-4. Orphanet J Rare Dis. 2017. PMID: 28859693 Free PMC article.

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