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Orphanet Journal of Rare Diseases|August 11, 2023
Efficacy confirmation study of aceneuramic acid administration for GNE myopathy in JapanMadoka Mori-Yoshimura, Naoki Suzuki, Masahisa Katsuno, et al.
Stem Cell Reports|March 22, 2016
Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem CellsNaoki Ichiyanagi, Koki Fujimori, Masato Yano, et al.
Neuromuscular Disorders : NMD|September 27, 2014
GNE myopathy associated with congenital thrombocytopenia: a report of two siblingsRumiko Izumi, Tetsuya Niihori, Naoki Suzuki, et al.
Brain : a Journal of Neurology|August 10, 2020
Aberrant interaction between FUS and SFPQ in neurons in a wide range of FTLD spectrum diseasesShinsuke Ishigaki, Yuichi Riku, Yusuke Fujioka, et al.
Orphanet Journal of Rare Diseases|November 9, 2016
Multicenter questionnaire survey for sporadic inclusion body myositis in JapanNaoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 24, 2020
AMPK Complex Activation Promotes Sarcolemmal Repair in DysferlinopathyHiroya Ono, Naoki Suzuki, Shin-Ichiro Kanno, et al.
Cell Reports|February 2, 2017
Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like PhenotypesShinsuke Ishigaki, Yusuke Fujioka, Yohei Okada, et al.
Orphanet Journal of Rare Diseases|June 28, 2019
The updated retrospective questionnaire study of sporadic inclusion body myositis in JapanNaoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, et al.
Plos One|August 1, 2024
Sporadic inclusion body myositis-derived myotube culture revealed muscle cell-autonomous expression profilesNaoki Suzuki, Makoto Kanzaki, Masashi Koide, et al.
Stem Cell Reports|May 28, 2021
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutationsShio Mitsuzawa, Naoki Suzuki, Tetsuya Akiyama, et al.
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