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Orphanet Journal of Rare Diseases|May 16, 2022
Tranilast for advanced heart failure in patients with muscular dystrophy: a single-arm, open-label, multicenter studyTsuyoshi Matsumura, Hiroya Hashimoto, Masahiro Sekimizu, et al.
Neuromuscular Disorders : NMD|September 4, 2018
Characteristic findings of skeletal muscle MRI in caveolinopathiesKumiko Ishiguro, Takahiro Nakayama, Masaru Yoshioka, et al.
Annals of Clinical and Translational Neurology|September 15, 2022
Metabolome and transcriptome analysis on muscle of sporadic inclusion body myositisAyuka Murakami, Seiya Noda, Tomoyuki Kazuta, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 19, 2024
Urinary titin reflects the severity of walking ability, muscle strength, and muscle and cardiac damage in patients with Becker muscular dystrophyHiroyuki Awano, Yoshinori Nambu, Kayo Osawa, 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.
American Journal of Human Genetics|December 27, 2016
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline MyopathySatoko Miyatake, Satomi Mitsuhashi, Yukiko K Hayashi, et al.
Neurobiology of Aging|December 19, 2020
The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathyTakashi Ando, Ryoichi Nakamura, Satoshi Kuru, et al.
Annals of Clinical and Translational Neurology|October 26, 2023
Natural history of Becker muscular dystrophy: a multicenter study of 225 patientsAkinori Nakamura, Tsuyoshi Matsumura, Katsuhisa Ogata, et al.
Science Advances|May 25, 2022
Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathologyKoyo Tsujikawa, Kohei Hamanaka, Yuichi Riku, et al.
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