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Muscular Dystrophy, Duchenne
Muscular Dystrophy, Animal
ANG1 treatment reduces muscle pathology and prevents a decline in perfusion in DMD mice.
Use of imaging biomarkers to assess perfusion and glucose metabolism in the skeletal muscle of dystrophic mice.
Molecular imaging to target transplanted muscle progenitor cells.
Application of 3-d echocardiography and gated micro-computed tomography to assess cardiomyopathy in a mouse model of duchenne muscular dystrophy.
High-frequency ultrasound to grade disease progression in murine models of Duchenne muscular dystrophy.
Skeletal muscle fibrosis in the mdx/utrn+/- mouse validates its suitability as a murine model of Duchenne muscular dystrophy.