Modeling disease trajectory in Duchenne muscular dystrophy

OBJECTIVE: To quantify disease progression in individuals with Duchenne muscular dystrophy (DMD) using magnetic resonance biomarkers of leg muscles. METHODS: MRI and magnetic resonance spectroscopy (MRS) biomarkers were acquired from 104 participants with DMD and 51 healthy controls using a prospect...

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Publicado no:Neurology
Main Authors: Rooney, William D., Berlow, Yosef A., Triplett, William T., Forbes, Sean C., Willcocks, Rebecca J., Wang, Dah-Jyuu, Arpan, Ishu, Arora, Harneet, Senesac, Claudia, Lott, Donovan J., Tennekoon, Gihan, Finkel, Richard, Russman, Barry S., Finanger, Erika L., Chakraborty, Saptarshi, O'Brien, Elliott, Moloney, Brendan, Barnard, Alison, Sweeney, H. Lee, Daniels, Michael J., Walter, Glenn A., Vandenborne, Krista
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7251517/
https://ncbi.nlm.nih.gov/pubmed/32184340
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000009244
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