Kawai M - Search Results

1

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: kawai m. 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.

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. Among authors: kawai m. Brain Nerve. 2011 Nov;63(11):1279-84. Brain Nerve. 2011. PMID: 22068481 Review. Japanese.

3

[Registry of muscular dystrophy (Remudy). Construction of the patient self-report registry and collaboration with overseas network].

Nakamura H, Kawai M. Nakamura H, et al. Among authors: kawai m. Rinsho Shinkeigaku. 2011 Nov;51(11):901-2. doi: 10.5692/clinicalneurol.51.901. Rinsho Shinkeigaku. 2011. PMID: 22277410 Japanese.

4

[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: kawai m. Rinsho Shinkeigaku. 2014;54(12):1069-70. doi: 10.5692/clinicalneurol.54.1069. Rinsho Shinkeigaku. 2014. PMID: 25519964 Review. Japanese.

5

[Survey of the actual state of medical care of patients with Duchenne muscular dystrophy in Japan].

Matsumura T, Komaki H, Kawai M. Matsumura T, et al. Among authors: kawai m. Rinsho Shinkeigaku. 2015;55(9):637-45. doi: 10.5692/clinicalneurol.cn-000736. Epub 2015 Jul 7. Rinsho Shinkeigaku. 2015. PMID: 26156259 Japanese.

6

Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan.

Saito T, Kawai M, Kimura E, Ogata K, Takahashi T, Kobayashi M, Takada H, Kuru S, Mikata T, Matsumura T, Yonemoto N, Fujimura H, Sakoda S. Saito T, et al. Among authors: kawai m. Neuromuscul Disord. 2017 Feb;27(2):107-114. doi: 10.1016/j.nmd.2016.11.012. Epub 2016 Nov 25. Neuromuscul Disord. 2017. PMID: 28003112 Clinical Trial.

7

Decreased resting energy expenditure in patients with Duchenne muscular dystrophy.

Shimizu-Fujiwara M, Komaki H, Nakagawa E, Mori-Yoshimura M, Oya Y, Fujisaki T, Tokita Y, Kubota N, Shimazaki R, Sato K, Ishikawa T, Goto K, Mochizuki H, Takanoha S, Ogata K, Kawai M, Konagaya M, Miyazaki T, Tatara K, Sugai K, Sasaki M. Shimizu-Fujiwara M, et al. Among authors: kawai m. Brain Dev. 2012 Mar;34(3):206-12. doi: 10.1016/j.braindev.2011.05.005. Epub 2011 May 31. Brain Dev. 2012. PMID: 21632191

8

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. Among authors: kawai m. 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.

9

[Nasal flaring during hypoxemia in myotonic dystrophy and duchenne muscular dystrophy].

Suzuki M, Oya Y, Murakami Y, Ogawa M, Kawai M. Suzuki M, et al. Among authors: kawai m. Rinsho Shinkeigaku. 2009 May;49(5):278-80. doi: 10.5692/clinicalneurol.49.278. Rinsho Shinkeigaku. 2009. PMID: 19594107 Japanese.

10

[Changes in clinical condition and causes of death of inpatients with Duchenne muscular dystrophy in Japan from 1999 to 2012].

Saito T, Tatara K, Kawai M. Saito T, et al. Among authors: kawai m. Rinsho Shinkeigaku. 2014;54(10):783-90. doi: 10.5692/clinicalneurol.54.783. Rinsho Shinkeigaku. 2014. PMID: 25342011 Japanese.

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