Becker muscular dystrophy (BMD) is an X-linked recessive disorder caused by dystrophin
gene mutations. The phenotype and evolution of this muscle disorder are extremely clinical …

Becker muscular dystrophy (BMD) is a neuromuscular disorder allelic to Duchenne
muscular dystrophy (DMD), caused by in-frame mutations in the dystrophin gene, and …

Introduction: With the advent of emerging molecular therapies for muscular dystrophies, the
need for knowledge about natural history course of such diseases is of utmost importance in …

Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …

Abstract Introduction/Aims Becker muscular dystrophy (BMD) is characterized by variable
disease severity and progression, prompting the identification of biomarkers for clinical trials …

Becker muscular dystrophy (BMD) is a genetic disease caused by an X-linked recessive
mutation leading to a defective dystrophin expression, with a relatively mild clinical course …

Our objective was to investigate the potential of three microRNAs, miR-181a-5p, miR-30c-
5p, and miR-206 as prognostic biomarkers for long-term follow up of Duchenne muscular …

Abstract Background and purpose Because Becker muscular dystrophy (BMD) is a
heterogeneous disease and only few studies have evaluated adult patients, it is currently …

Introduction: There is little information on magnetic resonance imaging (MRI) phenotypes of
Becker muscular dystrophy (BMD). This study presents the MRI phenotyping of the upper …

Becker muscular dystrophy (BMD) is a severe X-linked muscle disease. Age of onset,
clinical variability, speed of progression and affected tissues display wide variability, making …