treat population. Data are presented as LSM values ± 95% CI.c, Line graph showing LSM change from baseline to week 52 in TTR, seconds, for delandistrogene moxeparvovec (n = 63) and placebo (n = 61) groups in the modified intent-to-treat population. Data are presented as ...
A graph-matching kernel for object categorizationSegmentation by transductionRespiratory Care of the Patient with Duchenne Muscular DystrophyThe Duchenne smile: Emotional expression and brain physiology: II.The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of...
Objectives: Increasing fibrosis of skeletal muscle is a hallmark of the dystrophic process in Duchenne muscular dystrophy (DMD) and is a hindrance to functional muscle regeneration. We sought to evaluate the capacity of magnetic resonance elastography (MRE) to characterize the elastic properties of ...
Collins, C. A. & Morgan, J. E. Duchenne’s muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.Int. J. Exp. Pathol.84, 165–172 (2003). ArticleCASGoogle Scholar Cooper, B. J. Animal models of Duchenne and Becker muscular dystrophy.Br. Med...
A graph-matching kernel for object categorization Segmentation by transduction Respiratory Care of the Patient with Duchenne Muscular Dystrophy The Duchenne smile: Emotional expression and brain physiology: II. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with ty...
Duchenne muscular dystrophy (DMD) is an incurable neuromuscular disease leading to progressive skeletal muscle weakness and fatigue. Cell transplantation in murine models has shown promise in supplementing the lack of the dystrophin protein in DMD muscles. However, the establishment of novel, long-term...
Duchenne muscular dystrophy (DMD) is a neuromuscular disorder causing progressive muscle degeneration. Although cardiomyopathy is a leading mortality cause in DMD patients, the mechanisms underlying heart failure are not well understood. Previously, we showed that NF-κB exacerbates DMD skeletal muscle pat...
Duchenne muscular dystrophy (DMD), an X-linked disorder affects approximately 1 in 5000 males, is universally associated with heart disease. We previously identified myocardial disease by late gadolinium enhancement (LGE) in DMD subjects at various stages of disease, but the true prevalence is unclea...
Articles Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study Sebahattin Cirak*, Virginia Arechavala-Gomeza*, Michela Guglieri, Lucy Feng, Silvia Torelli, ...
Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoformDuchenne muscular dystrophyDiffusion MRIDp140 isoformGraph theoryNetwork-based statisticsNeuropsychological assessmentStructural connectome...