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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發表在: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
格式: Artigo
語言:Inglês
出版: Lippincott Williams & Wilkins 2020
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在線閱讀: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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