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Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2013
Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophyTakahiro Yonekawa, Hirofumi Komaki, Mari Okada, et al.
Brain : a Journal of Neurology|July 27, 2014
Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model miceTakahiro Yonekawa, May Christine V Malicdan, Anna Cho, et al.
Epilepsy & Behavior : E&B|October 8, 2011
Effect of corpus callosotomy on attention deficit and behavioral problems in pediatric patients with intractable epilepsyTakahiro Yonekawa, Eiji Nakagawa, Eri Takeshita, et al.
Science Advances|May 25, 2022
Large1 gene transfer in older myd mice with severe muscular dystrophy restores muscle function and greatly improves survivalTakahiro Yonekawa, Adam J Rauckhorst, Sara El-Hattab, et al.
Journal of Human Genetics|November 11, 2016
Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder alleleWenhua Zhu, Satomi Mitsuhashi, Takahiro Yonekawa, et al.
Biorxiv : the Preprint Server for Biology|January 8, 2024
Identification of a short, single site matriglycan that maintains neuromuscular function in the mouseTiandi Yang, Ishita Chandel, Miguel Gonzales, et al.
Aging|July 11, 2025
National survey of Hutchinson-Gilford progeria syndrome and progeroid laminopathy in JapanYuko Okawa, Muneaki Matsuo, Rika Kosaki, et al.
Elife|September 25, 2020
POMK regulates dystroglycan function via LARGE1-mediated elongation of matriglycanAmeya S Walimbe, Hidehiko Okuma, Soumya Joseph, et al.
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