What researchers published on Duchenne muscular dystrophy
735 papers, newest first.
Showing 40 of 735
ReviewNewborn Screening for Duchenne Muscular Dystrophy: Contemporary Considerations for Implementation of an Early Diagnostic Paradigm.Neurology
Not labelled yetAdvancing Clinical Trials and Precision Medicine in Duchenne Muscular Dystrophy Using Machine Learning-Based Trajectory Modeling and MRI Radiomics.Clinical pharmacology and therapeutics
Not labelled yetNeurochemical signatures of morphometric network reorganization in Duchenne muscular dystrophy: Links to cognition and behavior.Progress in neuro-psychopharmacology & biological psychiatry
Case reportA late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26-34 deletion: a case report.BMC neurology
Not labelled yetThe prevalence of Duchenne/Becker muscular dystrophy in the Russian Federation.Frontiers in genetics
Case reportDelayed Recognition of Duchenne Muscular Dystrophy During an Acute Respiratory Illness in an 11-Year-Old Boy: A Case Report.Cureus
Not labelled yetSpatial transcriptomics maps region and isoform specific brain alterations in mdx and mdx4cv models of Duchenne muscular dystrophy.Neurobiology of disease
Trial resultA 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
Not labelled yetWillingness to adopt gene therapy for Duchenne muscular dystrophy: barriers, facilitators, and multidisciplinary readiness.Frontiers in medicine
Not labelled yetNon-invasive adjunctive diagnostic models incorporating high-frequency ultrasound and shear wave elastography for pediatric Duchenne muscular dystrophy.Frontiers in genetics
Not labelled yetNon-invasive assessment of microvascular changes in a Duchenne muscular dystrophy rat model with near-infrared spectroscopy.Neuromuscular disorders : NMD
ReviewEfficacy and safety of exon skipping therapies for Duchenne Muscular Dystrophy: A Systematic Review.European journal of medical genetics
Not labelled yetA single liver-sparing myotropic AAV ameliorates muscular dystrophy in humanized mice by base editing.The Journal of clinical investigation
Not labelled yetDoes β-hydroxy-β-methylbutyrate-associated improvement in mitochondrial respiration preserve fast-twitch muscle function in Duchenne muscular dystrophy?The Journal of physiology
Not labelled yetExploring the relationship among nutrition, gut microbiota and musculoskeletal health in children with Duchenne muscular dystrophy: a cross-sectional study.European journal of nutrition
Case reportEarly-onset medication-related osteonecrosis of the jaw in adolescents with Duchenne muscular dystrophy receiving long-term antiresorptive combined with glucocorticoid therapy: Two case reports.Bone reports
Not labelled yetNiche-reprogramming CAR T therapy improves skeletal muscle regeneration and function in preclinical murine models of Duchenne muscular dystrophy.Cell stem cell
Not labelled yetCaregivers perspectives on multidisciplinary clinic visits for Duchenne and Becker muscular dystrophy.Journal of neuromuscular diseases
Not labelled yetEarly Cardiac Dysfunction in Pediatric Becker Muscular Dystrophy: A Prospective Cross-sectional Echocardiographic Study.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
Not labelled yetMuscle function, linear growth, and bone health during 30 months of vamorolone, prednisone, and deflazacort treatment for Duchenne muscular dystrophy: a comparative study.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Not labelled yetDeciphering isonicotinylation and mast cell-associated pathogenic patterns in Duchenne muscular dystrophy: evidence from ensemble learning-driven multi-omics and in vitro validation.Frontiers in molecular biosciences
Not labelled yetPhenotype rescue through the restoration of full-length dystrophin using CRISPR/Cas9 genome editing in Duchenne muscular dystrophy patient-derived iPSCs carrying the deletion of two exons.Genome medicine
Not labelled yetThree-Year Follow-Up of Delandistrogene Moxeparvovec in Duchenne Muscular Dystrophy: Long-Term Phase 3 EMBARK Trial Results.Neurology and therapy
ReviewChronic Inflammation, Fibrotic Remodeling, and Regenerative Failure in Duchenne Muscular Dystrophy: Mechanisms and Therapeutic Opportunities.Biomedicines
Not labelled yetParticipation Patterns of Youth With Duchenne-Becker Muscular Dystrophies Across Four Settings.Canadian journal of occupational therapy. Revue canadienne d'ergotherapie
Not labelled yetReduced Sperm Counts in Mice with Dmd Exon 51 Frameshift Mutations.Genes
Not labelled yetClinical Trial Landscape of Duchenne Muscular Dystrophy in Europe: A 10-Year Retrospective Analysis.Medicina (Kaunas, Lithuania)
Not labelled yetIn vivo genome-editing therapy for Duchenne muscular dystrophy: Preclinical studies and first-in-human trial.Cell
Not labelled yetVentilation inhomogeneity in Duchenne muscular dystrophy before the initiation of ventilatory support: Insights from electrical impedance tomography.Pulmonology
Not labelled yetTeaching NeuroImage: Somatic DMD Gene Mosaicism Causing Hemiatrophy in an Adult Man With Duchenne Muscular Dystrophy.Neurology
PreprintThe annexin A1 mimetic peptide Ac2-26 promotes inflammation-resolution and stimulates skeletal muscle regeneration in the mdx mouse model of Duchenne muscular dystrophy.bioRxiv : the preprint server for biology
PreprintStructural engineering of dual-targeting antisense oligonucleotides enhances exon 44 skipping for treating Duchenne muscular dystrophy.bioRxiv : the preprint server for biology
Case reportMissed Perforated Appendicitis in a Nonverbal Patient with Autism and Duchenne Muscular Dystrophy: A Case Report.Reports (MDPI)
Not labelled yetHMB as a therapeutic strategy in Duchenne muscular dystrophy: Linking muscle function, protein homeostasis and mitochondrial bioenergetics.The Journal of physiology
Not labelled yetMolecular Hybrids of Deflazacort and H2S Donors: From Bench to Potential Treatment for Duchenne Muscular Dystrophy.Journal of medicinal chemistry
Not labelled yetMachine Learning Integrating Quantitative MRI and Clinical Features Predicts Loss of Ambulation in Duchenne Muscular Dystrophy.Journal of cachexia, sarcopenia and muscle
Not labelled yetTwenty years of givinostat in Duchenne muscular dystrophy: a patient-organisation perspective.Neuromuscular disorders : NMD
Review[Duchenne muscular dystrophy-associated cardiomyopathy: advances in diagnosis and management].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
ReviewProgress on Duchenne muscular dystrophy: from molecular mechanisms to therapeutic strategies.Yi chuan = Hereditas
ReviewBrain imaging in dystrophinopathies.Journal of neurology