Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype: Cell
Causes/Inheritance - Duchenne Muscular Dystrophy (DMD) - Diseases | Muscular Dystrophy Association
JCI Insight - Duchenne muscular dystrophy hiPSC–derived myoblast drug screen identifies compounds that ameliorate disease in mdx mice
Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis | Orphanet Journal of Rare Diseases | Full Text
PDF) Risk assessment and genetic counseling in families with Duchenne muscular dystrophy
Frontiers | Current Pharmacological Strategies for Duchenne Muscular Dystrophy
Current pharmacological strategies for Duchenne muscular dystrophy. | Download Scientific Diagram
Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy | Neurología (English Edition)
RISCALW: A Windows Program for Risk Calculation in Families with Duchenne Muscular Dystrophy
Genetics: An introduction to Risk Analysis in X-linked Recessive Disorders
Genetics: An introduction to Risk Analysis in X-linked Recessive Disorders
Degenerative and regenerative pathways underlying Duchenne muscular dystrophy revealed by single-nucleus RNA sequencing | PNAS
Bayesian Analysis and Risk Assessment in Genetic Counseling and Testing - ScienceDirect
EMQN best practice guidelines for genetic testing in dystrophinopathies | European Journal of Human Genetics
Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy - The Journal of Pediatrics
Chronic pain, psychological distress, and quality of life in males with Duchenne muscular dystrophy - Huang - Developmental Medicine & Child Neurology - Wiley Online Library
An Alzheimer's Disease Genetic Risk Score Predicts Longitudinal Thinning of Hippocampal Complex Subregions in Healthy Older Adults | eNeuro
PDF) Risk assessment and genetic counseling in families with Duchenne muscular dystrophy
Report on the workshop: Meaningful outcome measures for Duchenne muscular dystrophy, London, UK, 30–31 January 2017 - Neuromuscular Disorders
IJNS | Free Full-Text | A Roadmap to Newborn Screening for Duchenne Muscular Dystrophy | HTML
Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophy - Zambon - 2022 - Developmental Medicine & Child Neurology - Wiley Online Library
Genetic Risk Assessment" by Bruce Korf for OPENPediatrics - YouTube
Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy - Helderman‐van den Enden - 2009 - Clinical Genetics - Wiley Online Library
Serum miRNAs as biomarkers for the rare types of muscular dystrophy - Neuromuscular Disorders
Screening of Duchenne Muscular Dystrophy (DMD) Mutations and Investigating Its Mutational Mechanism in Chinese Patients | PLOS ONE
COVID-19 Recommendations for the Duchenne Community - Parent Project Muscular Dystrophy
