What researchers published on Duchenne-izomdisztrófia
3455 papers, newest first.
Showing 20 of 3455
ÁttekintésCardioprotection and Heart Failure Management in Duchenne and Becker Muscular Dystrophies: A State-of-the-Art Review Across Pediatric and Transitional Age.Journal of clinical medicine
Daytime Mouthpiece Ventilation Combined with Nocturnal Non-Invasive Ventilation in Adults with Duchenne Muscular Dystrophy: A 30-Day Pilot Feasibility Study.Journal of clinical medicine
The longer, the better? Optimizing dystrophin constructs for cardiac gene therapy in Duchenne muscular dystrophy.Molecular therapy. Advances
ÁttekintésModeling bone abnormalities in Duchenne muscular dystrophy: Skeletal phenotypes, glucocorticoid responses, and translational considerations.Bone
Longitudinal pulmonary outcomes after posterior spinal fusion in Duchenne muscular dystrophy: a retrospective cohort study.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie
ÁttekintésNewborn Screening for Duchenne Muscular Dystrophy: Contemporary Considerations for Implementation of an Early Diagnostic Paradigm.Neurology
Advancing Clinical Trials and Precision Medicine in Duchenne Muscular Dystrophy Using Machine Learning-Based Trajectory Modeling and MRI Radiomics.Clinical pharmacology and therapeutics
Neurochemical signatures of morphometric network reorganization in Duchenne muscular dystrophy: Links to cognition and behavior.Progress in neuro-psychopharmacology & biological psychiatry
EsetismertetésA late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26-34 deletion: a case report.BMC neurology
The prevalence of Duchenne/Becker muscular dystrophy in the Russian Federation.Frontiers in genetics
EsetismertetésDelayed Recognition of Duchenne Muscular Dystrophy During an Acute Respiratory Illness in an 11-Year-Old Boy: A Case Report.Cureus
Spatial transcriptomics maps region and isoform specific brain alterations in mdx and mdx4cv models of Duchenne muscular dystrophy.Neurobiology of disease
Vizsgálati eredményA pre-post single-arm pilot trial of a digital multicomponent intervention for self-efficacy enhancement among online support groups of primary caregivers of children with neuro-muscular disorders: SEE-NMD protocol.PloS one
Willingness to adopt gene therapy for Duchenne muscular dystrophy: barriers, facilitators, and multidisciplinary readiness.Frontiers in medicine
Non-invasive adjunctive diagnostic models incorporating high-frequency ultrasound and shear wave elastography for pediatric Duchenne muscular dystrophy.Frontiers in genetics
Non-invasive assessment of microvascular changes in a Duchenne muscular dystrophy rat model with near-infrared spectroscopy.Neuromuscular disorders : NMD
ÁttekintésEfficacy and safety of exon skipping therapies for Duchenne Muscular Dystrophy: A Systematic Review.European journal of medical genetics
A single liver-sparing myotropic AAV ameliorates muscular dystrophy in humanized mice by base editing.The Journal of clinical investigation
Does β-hydroxy-β-methylbutyrate-associated improvement in mitochondrial respiration preserve fast-twitch muscle function in Duchenne muscular dystrophy?The Journal of physiology
Exploring the relationship among nutrition, gut microbiota and musculoskeletal health in children with Duchenne muscular dystrophy: a cross-sectional study.European journal of nutrition