Background: Becker muscular dystrophy is an X-linked, genetic disorder causing
progressive degeneration of skeletal and cardiac muscle, with a widely variable phenotype …

Background Analysis of muscle biopsies allowed to characterize the pathophysiological
changes of Duchenne and Becker muscular dystrophies (D/BMD) leading to the clinical …

ABSTRACT Introduction The phenotype of Becker muscular dystrophy (BMD) is highly
variable, and the disease may be underdiagnosed. We searched for new mutations in the …

[Late onset Becker muscular dystrophy. A case report and literature review]. - Abstract - Europe
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Noninvasive biomarkers with diagnostic value and prognostic applications have long been
desired to replace muscle biopsy for Duchenne muscular dystrophy (DMD) patients …

The differential diagnosis between autosomal recessive limb-girdle (LGMD) and X-linked
Becker muscular dystrophy (BMD) is very important for genetic counseling. It has been …

Aims Becker muscular dystrophy (BMD) is a genetic neuromuscular disease characterized
by an alteration of the dystrophin protein. Myocardial involvement is frequent, eventually …

Becker muscular dystrophy (BMD) is the milder allelic variant of Duchenne muscular
dystrophy, with higher dystrophin levels. To anticipate on results of interventions targeting …

Objective The transcriptional heterogeneity at a single‐nucleus level in human Becker
muscular dystrophy (BMD) dystrophic muscle has not been explored. Here, we aimed to …

Becker Muscular Dystrophy (BMD) is a rare X-linked recessive neuromuscular disorder
frequently caused by in-frame deletions in the DMD gene that result in the production of a …