Disease: Becker muscular dystrophy
- A novel deep intronic variant introduce dystrophin pseudoexon in Becker muscular dystrophy: A case report
- AAV-Mediated Restoration of Dystrophin-Dp71 in the Brain of Dp71-Null Mice: Molecular, Cellular and Behavioral Outcomes
- Age-associated sleep spindle characteristics in Duchenne muscular dystrophy
- Ambulatory electrocardiographic longitudinal monitoring in a canine model for Duchenne muscular dystrophy identifies decreased very low frequency power as a hallmark of impaired heart rate variability
- Amelioration of Morphological Pathology in Cardiac, Respiratory, and Skeletal Muscles Following Intraosseous Administration of Human Dystrophin Expressing Chimeric (DEC) Cells in Duchenne Muscular Dystrophy Model
- Anti-apoptotic protein Bcl-2 contributes to the determination of reserve cells during myogenic differentiation of C2C12 cells
- Apelin stimulation of the vascular skeletal muscle stem cell niche enhances endogenous repair in dystrophic mice
- Arrhythmias and cardiac MRI associations in patients with established cardiac dystrophinopathy
- Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy
- Atrogin-1 promotes muscle homeostasis by regulating levels of endoplasmic reticulum chaperone BiP
- Author Correction: miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy
- Brain Alteration Patterns in Children with Duchenne Muscular Dystrophy: A Machine Learning Approach to Magnetic Resonance Imaging
- Cardioprotection and Suppression of Fibrosis by Diverse Cancer and Non-Cancer Cell Lines in a Murine Model of Duchenne Muscular Dystrophy
- Casimersen (AMONDYS 45): An Antisense Oligonucleotide for Duchenne Muscular Dystrophy
- Chromosome Transplantation: Opportunities and Limitations
- Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies
- Comments on 'Life-threatening bowel complications in adults with Duchenne muscular dystrophy: a case series'
- Comments on 'Life-threatening bowel complications in adults with Duchenne muscular dystrophy: A case series' - Response
- Comparison of energy expenditure of individuals with Duchenne muscular dystrophy in the sitting posture on the ground and in water
- Comprehensive analysis of genomic complexity in the 5' end coding region of the DMD gene in patients of exons 1-2 duplications based on long-read sequencing
- Computer-Aided Diagnosis of Duchenne Muscular Dystrophy Based on Texture Pattern Recognition on Ultrasound Images Using Unsupervised Clustering Algorithms and Deep Learning
- Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology
- Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse
- Cross-species human disease modeling using patient-derived extracellular vesicles
- Cross-species modeling of muscular dystrophy in Caenorhabditis elegans using patient-derived extracellular vesicles
- Current Strategies for Increasing Knock-In Efficiency in CRISPR/Cas9-Based Approaches
- De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis
- Differential metabolic secretion between mdx mouse-derived spindle cell sarcomas and rhabdomyosarcomas drives tumor type development
- Diffusion tensor imaging reveals subclinical alterations in muscles of patients with becker muscular dystrophy
- Drp1 controls complex II assembly and skeletal muscle metabolism by Sdhaf2 action on mitochondria
- Duchenne muscular dystrophy caused by a deletion (c.5021del) in exon 35 of the DMD gene: A case report and review of the literature
- Editorial: Development of the precision diagnostics and treatment for duchenne/becker muscular dystrophy
- Efficacy and Tolerability of Ivabradine for Cardiomyopathy in Patients with Duchenne Muscular Dystrophy
- Efficiency of CNV-seq in detecting fetal DMD gene deletion or duplication in prenatal diagnosis
- Electrocardiographic and Autonomic Nervous System Changes after Changes in the Posture of Children and Adolescents with Duchenne Muscular Dystrophy
- Enhanced Diaphragm Muscle Function upon Satellite Cell Transplantation in Dystrophic Mice
- Escaping from CRISPR-Cas-mediated knockout: the facts, mechanisms, and applications
- FDA approves an HDAC inhibitor for Duchenne muscular dystrophy
- Feasibility of virtual reality and comparison of its effectiveness to biofeedback in children with Duchenne and Becker muscular dystrophies
- Five multivariate Duchenne muscular dystrophy progression models bridging six-minute walk distance and MRI relaxometry of leg muscles
- Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids
- Functional cardiac consequences of beta-adrenergic stress-induced injury in the mdx mouse model of Duchenne muscular dystrophy
- Genetic therapies and respiratory outcomes in patients with neuromuscular disease
- HDAC inhibitors as pharmacological treatment for Duchenne muscular dystrophy: a discovery journey from bench to patients: (Trends in Molecular Medicine, 30:3 p:278-294, 2024)
- Heart in Disguise: Unmasking a Novel Gene Deletion in Dilated Cardiomyopathy
- Implication of Corneal Refractive Surgery in Duchenne Muscular Dystrophy
- Improved mitochondrial function in the heart of sarcolipin-deficient dystrophin and utrophin double knockout mice
- Inhibition of miR-25 ameliorates cardiac and skeletal muscle dysfunction in aged <em>mdx/utrn</em> haploinsufficient (+/-) mice
- Ion channels as biomarkers of altered myogenesis in myofiber precursors of Duchenne muscular dystrophy
- LEDT and Idebenone treatment modulate autophagy and improve regenerative capacity in the dystrophic muscle through an AMPK-pathway
- Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient-reported outcome measures
- Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene
- Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy
- Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy
- MCU-independent Ca(2+) uptake mediates mitochondrial Ca(2+) overload and necrotic cell death in a mouse model of Duchenne muscular dystrophy
- Mitochondria and Reactive Oxygen Species: The Therapeutic Balance of Powers for Duchenne Muscular Dystrophy
- Mitochondrial Transplantation Therapy Ameliorates Muscular Dystrophy in mdx Mouse Model
- Motor dysfunction of the gut in Duchenne muscular dystrophy: A review
- Muscle stem cell dysfunction in rhabdomyosarcoma and muscular dystrophy
- Neurocognitive functioning among children and young people with Duchenne Muscular Dystrophy: A systematic review and meta-analysis
- New therapeutic avenues for Duchenne muscular dystrophy
- Newborn screening for Duchenne muscular dystrophy: the perspectives of stakeholders
- Non-negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue
- Noninvasive twin genotyping for recessive monogenic disorders by relative haplotype dosage
- Novel mutation leading to splice donor loss in a conserved site of DMD gene causes Duchenne muscular dystrophy with cryptorchidism
- Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice
- Patient-reported impact of symptoms in adrenoleukodystrophy (PRISM-ALD)
- Population longitudinal analysis of Gait Profile Score and North Star Ambulatory Assessment in children with Duchenne muscular dystrophy
- Potential Therapeutic Targets for Hypotension in Duchenne Muscular Dystrophy
- Pragmatic Neurorehabilitation Approach for Improving Quality of Life in Duchenne Muscular Dystrophy: A Case Report
- Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis
- Preimplantation genetic testing for monogenic disorders (PGT-M) offers an alternative strategy to prevent children from being born with hereditary neurological diseases or metabolic diseases dominated by nervous system phenotypes: a retrospective study
- Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India
- Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants
- Respiratory comorbidities and treatments in Duchenne muscular dystrophy: impact on life expectancy and causes of death
- Right ventricular preload and afterload challenge induces contractile dysfunction and arrhythmia in isolated hearts of dystrophin-deficient male mice
- Safety and efficacy of givinostat in boys with Duchenne muscular dystrophy (EPIDYS): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
- Screening for Duchenne muscular dystrophy in newborns in the Ningxia region
- Severity of muscle impairment and its progression assessed using musculoskeletal magnetic resonance imaging and diffusion tension imaging in 78 boys with Duchenne muscular dystrophy: a retrospective study
- Spending on Targeted Therapies for Duchenne Muscular Dystrophy
- State of art of mobility medicine: some more abstracts and evidence that the success of Pdm3 is based on extra-session relationships
- Stride Velocity 95th Centile Detects Decline in Ambulatory Function Over Shorter Intervals than the 6-Minute Walk Test or North Star Ambulatory Assessment in Duchenne Muscular Dystrophy
- Sudden cardiac death in Duchenne muscular dystrophy
- Survival among patients receiving eteplirsen for up to 8 years for the treatment of Duchenne muscular dystrophy and contextualization with natural history controls
- The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot Study
- The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a novel model of Duchenne muscular dystrophy
- The complex landscape of DMD mutations: moving towards personalized medicine
- The exon junction complex is required for DMD gene splicing fidelity and myogenic differentiation
- The extracellular matrix differentially directs myoblast motility and differentiation in distinct forms of muscular dystrophy: Dystrophic matrices alter myoblast motility
- The Importance of a PM&R Consultation for Becker Muscular Dystrophy Patients Admitted with Cardiomyopathy
- The satellite cell in skeletal muscle: A story of heterogeneity
- The unconditioned fear response in vertebrates deficient in dystrophin
- Timed rolling and rising tests in Duchenne muscular dystrophy ambulant boys: a feasibility study
- Transcriptome-based deep learning analysis identifies drug candidates targeting protein synthesis and autophagy for the treatment of muscle wasting disorder
- Treatment with ataluren in four symptomatic Duchenne carriers. A pilot study
- Trends from two decades of orphan designations in paediatric rare neuromuscular diseases
- Trilobatin contributes to the improvement of myopathy in a mouse model of Duchenne muscular dystrophy
- Uncovering the Power of GPR18 Signalling: How RvD2 and Other Ligands Could Have the Potential to Modulate and Resolve Inflammation in Various Health Disorders
- Validity of the Functional Classification of the Upper Extremities for Duchenne Muscular Dystrophy
- Wireless Pulmonary Artery Pressure Monitor Implantation in a Patient with Duchenne Muscular Dystrophy