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Neuromuscular Disorders : NMD|October 28, 2008
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1)Sherine Shalaby, Yukiko K Hayashi, Kanako Goto, et al.
Plos One|March 18, 2014
Association between a C8orf13-BLK polymorphism and polymyositis/dermatomyositis in the Japanese population: an additive effect with STAT4 on disease susceptibilityTomoko Sugiura, Yasushi Kawaguchi, Kanako Goto, et al.
BMC Neurology|August 22, 2002
Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patientsTsuyoshi Matsumura, Kanako Goto, Gaku Yamanaka, et al.
Journal of the Neurological Sciences|March 31, 2004
FSHD-like patients without 4q35 deletionGaku Yamanaka, Kanako Goto, Tadayuki Ishihara, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 12, 2002
[The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene]Yasushi Onishi, Jun Higuchi, Tatuji Ogawa, et al.
Acta Neuropathologica|February 25, 2010
Congenital myotonic dystrophy can show congenital fiber type disproportion pathologyKayo Tominaga, Yukiko K Hayashi, Kanako Goto, et al.
Bone|March 27, 2025
Visualization and quantification of RANK-RANKL binding for application to disease investigations and drug discoveryKen-Ichi Nakahama, Shiho Hidaka, Kanako Goto, et al.
Experimental Physiology|November 22, 2018
Effect of increased inspiratory muscle work on blood flow to inactive and active limbs during submaximal dynamic exerciseKeisho Katayama, Kanako Goto, Kaori Shimizu, et al.
Annals of the Rheumatic Diseases|March 10, 2012
Positive association between STAT4 polymorphisms and polymyositis/dermatomyositis in a Japanese populationTomoko Sugiura, Yasushi Kawaguchi, Kanako Goto, et al.
Neuromuscular Disorders : NMD|April 11, 2016
Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutationsKohei Hamanaka, Kanako Goto, Mami Arai, et al.
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