Matsumoto M - Search Results

1

The prescription rates of glucagon for hypoglycemia by pediatricians and physicians are low in Japan.

Matsumoto M, Awano H, Hirota Y, Nagai M, Bo R, Matsuoka A, Hamaguchi T, Takeuchi T, Nakagawa Y, Ogawa W, Iijima K. Matsumoto M, et al. Endocrine. 2019 May;64(2):233-238. doi: 10.1007/s12020-018-1793-z. Epub 2018 Oct 26. Endocrine. 2019. PMID: 30367442

2

Dried umbilical cord is a potential material for retrospective diagnosis of intrauterine enterovirus infection.

Morioka I, Matsumoto M, Miwa A, Yokota T, Matsuo K, Koda T, Nagasaka M, Shibata A, Fujita K, Yamane M, Yamada H, Enomoto M, Chikahira M, Iijima K. Morioka I, et al. Among authors: matsumoto m. J Matern Fetal Neonatal Med. 2014 Nov;27(17):1820-2. doi: 10.3109/14767058.2013.879701. Epub 2014 Feb 3. J Matern Fetal Neonatal Med. 2014. PMID: 24433096 Free article.

3

A pediatric patient with interstitial pneumonia due to enterovirus D68.

Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K. Matsumoto M, et al. J Infect Chemother. 2016 Oct;22(10):712-5. doi: 10.1016/j.jiac.2016.03.009. Epub 2016 Apr 22. J Infect Chemother. 2016. PMID: 27118532

4

Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGS.

Niba ETE, Nishida A, Tran VK, Vu DC, Matsumoto M, Awano H, Lee T, Takeshima Y, Nishio H, Matsuo M. Niba ETE, et al. Among authors: matsumoto m. J Hum Genet. 2017 Apr;62(5):531-537. doi: 10.1038/jhg.2016.162. Epub 2017 Jan 19. J Hum Genet. 2017. PMID: 28100912

5

2'-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Chimera Antisense Oligonucleotides to Induce Dystrophin Exon 45 Skipping.

Lee T, Awano H, Yagi M, Matsumoto M, Watanabe N, Goda R, Koizumi M, Takeshima Y, Matsuo M. Lee T, et al. Among authors: matsumoto m. Genes (Basel). 2017 Feb 10;8(2):67. doi: 10.3390/genes8020067. Genes (Basel). 2017. PMID: 28208626 Free PMC article. Review.

6

DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification.

Niba ETE, Yamanaka R, Rani AQM, Awano H, Matsumoto M, Nishio H, Matsuo M. Niba ETE, et al. Among authors: matsumoto m. Cancer Cell Int. 2017 May 23;17:58. doi: 10.1186/s12935-017-0428-4. eCollection 2017. Cancer Cell Int. 2017. PMID: 28546788 Free PMC article.

7

Clinical features in very early-onset demyelinating disease with anti-MOG antibody.

Nishiyama M, Nagase H, Matsumoto M, Tomioka K, Awano H, Tanaka T, Toyoshima D, Fujita K, Maruyama A, Oyazato Y, Saeki K, Shiraishi K, Takada S, Kaneko K, Takahashi T, Nakashima I, Iijima K. Nishiyama M, et al. Among authors: matsumoto m. Brain Dev. 2017 Oct;39(9):756-762. doi: 10.1016/j.braindev.2017.05.004. Epub 2017 May 24. Brain Dev. 2017. PMID: 28551039

8

Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy.

Yamamoto T, Taniguchi-Ikeda M, Awano H, Matsumoto M, Lee T, Harada R, Imanishi T, Hayashi N, Sakai Y, Morioka I, Takeshima Y, Iijima K, Saegusa J, Toda T. Yamamoto T, et al. Among authors: matsumoto m. Brain Dev. 2017 Nov;39(10):861-868. doi: 10.1016/j.braindev.2017.05.008. Epub 2017 May 31. Brain Dev. 2017. PMID: 28578814

9

Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup.

Matsumoto M, Awano H, Lee T, Takeshima Y, Matsuo M, Iijima K. Matsumoto M, et al. Neuromuscul Disord. 2017 Nov;27(11):1023-1028. doi: 10.1016/j.nmd.2017.06.007. Epub 2017 Jun 19. Neuromuscul Disord. 2017. PMID: 28734761

10

Dystrophin Dp116: A yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene.

Matsuo M, Awano H, Matsumoto M, Nagai M, Kawaguchi T, Zhang Z, Nishio H. Matsuo M, et al. Among authors: matsumoto m. Genes (Basel). 2017 Oct 2;8(10):251. doi: 10.3390/genes8100251. Genes (Basel). 2017. PMID: 28974057 Free PMC article. Review.

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