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Muscle & Nerve|December 2, 2017
Cognitive impairment and quality of life in patients with myotonic dystrophy type 1Haruo Fujino, Honoka Shingaki, Shugo Suwazono, et al.BMC Neurology|May 25, 2026
Association between creatinine-to-cystatin C ratio and ALSFRS-R across clinical phenotypesYoshihisa Fujiwara, Akihiro Hashiguchi, Shiori Yamashiro, et al.Intractable & Rare Diseases Research|March 20, 2018
The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patientsNatsumi Fujisaki, Shugo Suwazono, Masahito Suehara, et al.Internal Medicine (Tokyo, Japan)|May 6, 2026
Association between the Loss of Ambulation and the Distal Aortic Diameter in Male Patients with Muscular Dystrophy: A CT-based Observational StudyYuichiro Ohya, Takashi Tokashiki, Masataka Yamashiro, et al.European Heart Journal Open|October 11, 2024
CTG repeat length underlying cardiac events and sudden death in myotonic dystrophy type 1Hideki Itoh, Takashi Hisamatsu, Kazuhiko Segawa, et al.Orphanet Journal of Rare Diseases|December 7, 2023
Higher dose alglucosidase alfa is associated with improved overall survival in infantile-onset Pompe disease (IOPD): data from the Pompe RegistryPriya S Kishnani, David Kronn, Shugo Suwazono, et al.Journal of the American Heart Association|August 20, 2020
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura, et al.Journal of the Peripheral Nervous System : JPNS|February 29, 2020
Clinical features of inherited neuropathy with BSCL2 mutations in JapanSatoshi Ishihara, Yuji Okamoto, Hajime Tanabe, et al.Neuromuscular Disorders : NMD|August 31, 2021
A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophyTsuyoshi Matsumura, Hiroto Takada, Michio Kobayashi, et al.Science Advances|July 15, 2026
Reduction of appearance artifacts in wearable on-skin electronicsYijun Liu, Soutaro Ito, Takeo Kato, et al.Pageof 3