Article
Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice.
Brain : a journal of neurology - 1 Oct 2014
Yonekawa Takahiro, Malicdan May Christine V, Cho Anna, Hayashi Yukiko K, Nonaka Ikuya, Mine Toshiki, Yamamoto Takeshi, Nishino Ichizo, Noguchi Satoru
Abstract excerpt
Patients with GNE myopathy, a progressive and debilitating disease caused by a genetic defect in sialic acid biosynthesis, rely on supportive care and eventually become wheelchair-bound. To elucidate whether GNE myopathy is treatable at a progressive stage of the disease, we examined the efficacy of sialic acid supplementation on symptomatic old GNE myopathy mice that have ongoing, active muscle degeneration. We...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
