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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Xehetasun bibliografikoak
Argitaratua izan da:Neurology
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Lippincott Williams & Wilkins 2020
Gaiak:
Article
Sarrera elektronikoa: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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