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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Foilsithe in: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
Formáid: Artigo
Teanga:Inglês
Foilsithe: Lippincott Williams & Wilkins 2020
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Article
Rochtain Ar Líne: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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