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Page 1
Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study.
Komaki H, Takeshima Y, Matsumura T, Ozasa S, Funato M, Takeshita E, Iwata Y, Yajima H, Egawa Y, Toramoto T, Tajima M, Takeda S. Komaki H, et al. Among authors: funato m. Ann Clin Transl Neurol. 2020 Dec;7(12):2393-2408. doi: 10.1002/acn3.51235. Epub 2020 Dec 7. Ann Clin Transl Neurol. 2020. PMID: 33285037 Free PMC article. Clinical Trial.
Efficacy of Prednisolone in Generated Myotubes Derived From Fibroblasts of Duchenne Muscular Dystrophy Patients.
Kameyama T, Ohuchi K, Funato M, Ando S, Inagaki S, Sato A, Seki J, Kawase C, Tsuruma K, Nishino I, Nakamura S, Shimazawa M, Saito T, Takeda S, Kaneko H, Hara H. Kameyama T, et al. Among authors: funato m. Front Pharmacol. 2018 Dec 3;9:1402. doi: 10.3389/fphar.2018.01402. eCollection 2018. Front Pharmacol. 2018. PMID: 30559667 Free PMC article.
Early phase 2 trial of TAS-205 in patients with Duchenne muscular dystrophy.
Komaki H, Maegaki Y, Matsumura T, Shiraishi K, Awano H, Nakamura A, Kinoshita S, Ogata K, Ishigaki K, Saitoh S, Funato M, Kuru S, Nakayama T, Iwata Y, Yajima H, Takeda S. Komaki H, et al. Among authors: funato m. Ann Clin Transl Neurol. 2020 Feb;7(2):181-190. doi: 10.1002/acn3.50978. Epub 2020 Jan 20. Ann Clin Transl Neurol. 2020. PMID: 31957953 Free PMC article. Clinical Trial.
A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy.
Matsumura T, Takada H, Kobayashi M, Nakajima T, Ogata K, Nakamura A, Funato M, Kuru S, Komai K, Futamura N, Adachi Y, Arahata H, Fukudome T, Ishizaki M, Suwazono S, Aoki M, Matsuura T, Takahashi MP, Sunada Y, Hanayama K, Hashimoto H, Nakamura H. Matsumura T, et al. Among authors: funato m. Neuromuscul Disord. 2021 Sep;31(9):839-846. doi: 10.1016/j.nmd.2021.04.008. Epub 2021 May 7. Neuromuscul Disord. 2021. PMID: 34462178 Free PMC article.
RNA-seq analysis, targeted long-read sequencing and in silico prediction to unravel pathogenic intronic events and complicated splicing abnormalities in dystrophinopathy.
Okubo M, Noguchi S, Awaya T, Hosokawa M, Tsukui N, Ogawa M, Hayashi S, Komaki H, Mori-Yoshimura M, Oya Y, Takahashi Y, Fukuyama T, Funato M, Hosokawa Y, Kinoshita S, Matsumura T, Nakamura S, Oshiro A, Terashima H, Nagasawa T, Sato T, Shimada Y, Tokita Y, Hagiwara M, Ogata K, Nishino I. Okubo M, et al. Among authors: funato m. Hum Genet. 2023 Jan;142(1):59-71. doi: 10.1007/s00439-022-02485-2. Epub 2022 Sep 1. Hum Genet. 2023. PMID: 36048237
152 results