医学博士, 信州大学

Clinical characteristics of patients with myalgia as the initial manifestation of small and medium-sized vasculitis: a retrospective study
Ushiyama S, ShimojimaY, Ueno K, Kishida D, Miyazaki D, Sekijima Y
Rheumatol Int, 40(10), 1667-1674, 2020

Comparison of the phenotypes of patients harboring in-frame deletions starting at exon 45 in the Duchenne muscular dystrophy gene indicates potential for the development of exon skipping therapy.
Nakamura A, Shiba N, Miyazaki D, Nishizawa H, Inaba Y, Fueki N, Maruyama R, Echigoya Y, Yokota T.
J Hum Genet, 62(4), 459-463, Apr. 2017

Increasing Incidence and Age at Onset of Amyotrophic Lateral Sclerosis in Nagano Prefecture, Japan
Chinatsu KOBAYASHI, Daigo MIYAZAKI, Tomomi KINOSHITA, Akiyo HINENO, Akinori NAKAMURA
信州医学雑誌, 64(5), 239-246, Nov. 2016

Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis.
Miyazaki D, Nakamura A, Hineno A, Kobayashi C, Kinoshita T, Yoshida K, Ikeda S.
Neurol Sci, 37(8), 1277-81, Aug. 2016

Deletion of exons 3-9 encompassing a mutational hot spot in the DMD gene presents an asymptomatic phenotype, indicating a target region for multiexon skipping therapy.
Nakamura A, Fueki N, Shiba N, Motoki H, Miyazaki D, Nishizawa H, Echigoya Y, Yokota T, Aoki Y, Takeda S.
J Hum Genet, 61(7), 663-7, Jul. 2016

Crossed Cerebellar Diaschisis in Status Epilepticus.
Miyazaki D, Fukushima K, Nakahara A, Kodaira M, Mochizuki K, Kaneko K, Kaneko T, Sekijima Y, Ikeda S.
Intern Med, 55(12), 1649-51, Jun. 2016

Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy.
1. Shiba N, Miyazaki D, Yoshizawa T, Fukushima K, Shiba Y, Inaba Y, Imamura M, Takeda S, Koike K, Nakamura A.
2015

Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers
Miyazaki, D; Nakamura, A; Fukushima, K; Yoshida, K; Takeda, S; Ikeda, S
HUMAN MOLECULAR GENETICS, 20(9), 1787-1799, May 2011

重症度の異なる複数のベッカー型筋ジストロフィーモデルマウスを用いた重症化機序に関する研究
宮崎大吾、佐藤充人、柴直子、吉沢隆浩、中村昭則
日本筋学会学術集会, 06 Aug. 2022

Study about genome editing mouse models carrying exon-deletion s of severe- and mild-form BMD
Daigo Miyazaki,Mitsuto Sato,Naoko Shiba,Takahiro Yoshizawa,Akinori Nakamura
日本神経学会学術大会, 18 May 2022

重症度の異なるエクソン欠失を持つゲノム編集マウスを用いたベッカー型筋ジストロフィー重症化に関する研究
宮崎大吾、佐藤充人、柴直子、吉沢隆浩、中村昭則
日本筋学会学術集会, 12 Dec. 2021

TMSB4X and IGF2 down-regulation in dystrophin-deficient cardiomyocyte derived from DMD
Daigo Miyazaki,Naoko Shiba,Mitsuto Sato,Yuji Shiba,Yusuke Echigoya,Toshifumi Yokota,Yoshitaka Mizobe,Yoshitsugu Aoki,Shinichi Takeda,Akinori Nakamura
日本神経学会学術大会, 22 May 2021

当科で経験したパーキンソン病患者におけるL-ドパ持続経腸療法の検討
池田淳司、近藤恭史、宮崎大吾、関島良樹
日本神経学会学術大会, 19 May 2021

Exon 45 skipping therapy of induced pluripotent stem cells from a DMD patient with exon 46-55 deletion
Mitsuto Sato, Daigo Miyazaki, Yuji Shiba, Yusuke Echigoya, Toshifumi Yokota, Yoshitsugu Aoki, Shin’ichi Takeda, Akinori Nakamura
World congress of neurology (WCN) 2017, Sep. 2017

Dystrophin-deficient cardiomyocyte derived from Duchenne Muscular Dystrophy specific induced pluripotent stem cells carrying the deletion of exon 46-55 in DMD gene
Daigo Miyazaki, Mitsuto Sato, Yuji Shiba, Yusuke Echigoya, Toshifumi Yokota, Yoshitsugu Aoki, Shinichi Takeda, Akinori Nakamura
World congress of neurology (WCN) 2017, Sep. 2017

Becker muscular dystrophyのDMD遺伝子変異Hot Spotにおける遺伝型一表現型の検討
宮崎 大吾, 中村 昭則, 柴 直子, 稲葉 雄二, 笛木 昇, 古庄 知己, 池田 修一
臨床神経学 56 Suppl. S420, Dec. 2016, 日本神経学会

Elevation of serum Heat-Shock Protein (HSP) 70 and 90 in patients with ALS
Daigo Miyazaki,1 Akinori Nakamura,1,2 Chinatsu Kobayashi,1 Tomomi Kinoshita,1 Akiyo Hineno,3 Kunihiro Yoshida,4 Shu-ichi Ikeda
日本神経学会総会, 2015

Elevated serum levels of Heat-Shock Protein (HSP) 70 and 90 in patients with ALS
Daigo Miyazaki,1 Akinori Nakamura,1,2 Chinatsu Kobayashi,1 Tomomi Kinoshita,1 Akiyo Hineno,3 Kunihiro Yoshida,4 Shu-ichi Ikeda
World conress of neurology 2015. chile, 2015