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Qualitative and quantitative muscle ultrasound in patients with Duchenne muscular dystrophy: Where do sonographic changes begin?

Vill, K. ; Sehri, M. ; Müller, C. ; Hannibal, I. ; Huf, V. ; Idriess, M. ; Gerstl, L. ; Bonfert, M.V. ; Tacke, M. ; Schroeder, A.S. ; Landgraf, M.N. ; Müller-Felber, W. ; Blaschek, A.


Objective: The number of studies investigating and understanding the disease mechanisms of Duchenne muscular dystrophy (DMD) in human clinical trials have increased substantially over the last decade. Suitable clinical instruments for the measurement of disease progress and drug efficiency are mandatory, but currently not available, especially in the youngest patients. The aim of this study was ...


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