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Muscle & Nerve|January 26, 2019
The myotonic dystrophy health index: Japanese adaption and validity testingItsuki Mori, Haruo Fujino, Tsuyoshi Matsumura, et al.Journal of the Neurological Sciences|October 7, 2008
A cross-sectional study for glucose intolerance of myotonic dystrophyTsuyoshi Matsumura, Hiromi Iwahashi, Tohru Funahashi, et al.Acta Neuropathologica|July 31, 2007
Endoplasmic reticulum stress in myotonic dystrophy type 1 muscleKoji Ikezoe, Masayuki Nakamori, Hirokazu Furuya, et al.Human Molecular Genetics|August 31, 2007
Molecular mechanisms responsible for aberrant splicing of SERCA1 in myotonic dystrophy type 1Shin-Ichiro Hino, Shinichi Kondo, Hiroshi Sekiya, et al.Human Molecular Genetics|June 24, 2005
Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1Takashi Kimura, Masayuki Nakamori, John D Lueck, et al.Pediatric Neurology|March 1, 2015
Phenotypic variability in childhood of skeletal muscle sodium channelopathiesHarumi Yoshinaga, Shunichi Sakoda, Takashi Shibata, et al.Disability and Rehabilitation|March 31, 2024
Facioscapulohumeral muscular dystrophy Health Index: Japanese translation and validation studyHaruo Fujino, Masanori P Takahashi, Harumasa Nakamura, et al.Journal of the Neurological Sciences|January 20, 2012
A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodesHarumi Yoshinaga, Shunichi Sakoda, Jean-Marc Good, et al.Biology of the Cell|March 5, 2008
S1-1 nuclear domains: characterization and dynamics as a function of transcriptional activityAkira Inoue, Katsuji Tsugawa, Kazuaki Tokunaga, et al.Journal of the Neurological Sciences|September 23, 2016
A case of non-dystrophic myotonia with concomitant mutations in the SCN4A and CLCN1 genesHideki Kato, Yosuke Kokunai, Carine Dalle, et al.Pageof 15