← All diseases
Muscles and connective tissue
Becker muscular dystrophy
Do you want to be notified when there is new research about Becker muscular dystrophy? This is possible with an account. Create a free account or log in.
Automatically tracked from PubMed and ClinicalTrials.gov, newest on top. Nothing ever disappears here: what you keep in your favorites remains findable. · RSS feed of this disease · only the strongest evidence
Read in plain language what each study is about? With Premium, above each publication there is one sentence that explains what was investigated — and you receive a notification as soon as there is new research about Becker muscular dystrophy. View what Premium costs.
Publications and studies (1748)
- An underestimated factor for therapeutic decision-making in rare diseases: parents' (un)knowledge-the example of Duchenne muscular dystrophy caregivers and non-invasive ventilation. (2025/06/05) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Neurology of Androgens and Androgenic Supplements. (2025/06/03) ♡
- The prospective acceptability of preventative IV bisphosphonate therapy prior to fracture: Perspectives of young people with Duchenne muscular dystrophy, parents and health professionals. (2025/06/02) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Decoding Neuromuscular Disorders: The Complex Role of Genetic and Epigenetic Regulators. (2025/05/23) ♡
- The use of protein supplements in children with cerebral palsy: A scoping literature review. (2025/05/08) ♡
- Survival in Duchenne muscular dystrophy in Australia: a 50 year retrospective cohort study. (2025/05/08) ♡
- Meta-analysisiAll studies on one question combined and calculated together. This is the strongest form of research that exists: a single loose study can be coincidence, dozens together much less so. The label says something about the design, not about the outcome — which can also be that something does NOT work. Meta-analysis of the efficacy and safety of vamorolone in Duchenne muscular dystrophy. (2025/05/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. In Vivo-Like Scaffold-Free 3D In Vitro Models of Muscular Dystrophies: The Case for Anchored Cell Sheet Engineering in Personalized Medicine. (2025/05/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The Potential of Targeting APE1/Ref-1 as a Therapeutic Intervention for Duchenne Muscular Dystrophy. (2025/05/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Potential of synergist ablation to study mechanisms of skeletal muscle hypertrophy in rodent disease models. (2025/05/01) ♡
- The use of bisphosphonate and testosterone in young people with Duchenne muscular dystrophy: an international clinician survey. (2025/04/25) ♡
- A novel ex vivo protocol that mimics length and excitation changes of human muscles during walking induces force losses in EDL but not in soleus of mdx mice. (2025/04/07) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Dr. Peter Emil Becker and the Third Reich: Correspondence. (2025/04/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Is Duchenne gene therapy a suitable treatment despite its immunogenic class effect? (2025/04/01) ♡
- Successful oral surgery under general anesthesia for a patient with Duchenne muscular dystrophy presenting with mandibular fracture: A case report. (2025/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Complex glycerol kinase deficiency: A case report. (2025/04/01) ♡
- Incidence of Radiologically Confirmed Fractures in Adults With Duchenne Muscular Dystrophy. (2025/04/01) ♡
- Physical activity and cardiac function in patients with Duchenne muscular dystrophy. (2025/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Genetic and Clinical Characterization of Complex Glycerol Kinase Deficiency in Two Male Siblings: A Case Report. (2025/03/31) ♡
- Time Release Ion Matrix Regenerates Dystrophic Skeletal Muscle. (2025/03/20) ♡
- Evaluation of a six-minute walk test in the DE50-MD canine model of Duchenne muscular dystrophy and its effect on blood-borne biomarkers. (2025/03/17) ♡
- Cardiac implications of chicken wooden breast myopathy. (2025/03/05) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Reduced voltage-activated Ca2+ release flux in muscle fibers from a rat model of Duchenne dystrophy. (2025/03/03) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. A New Perspective on Drugs for Duchenne Muscular Dystrophy: Proposals for Better Respiratory Outcomes and Improved Regulatory Pathways. (2025/03/01) ♡
- Early-stage study (phase 1 or 2)iEarly research in a small group, primarily aimed at safety and dosage. Whether it actually works still needs to be determined afterward. Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy. (2025/03/01) ♡
- Gaps in the Assessment and Care of Neurodevelopmental and Psychiatric Conditions Associated With Dystrophinopathy. (2025/03/01) ♡
- Physical Activity Correlates With Skeletal Muscle MRI Findings in Individuals With Duchenne Muscular Dystrophy. (2025/03/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Taking ACTION to detect myocarditis related to recombinant gene transfer therapy for Duchenne Muscular Dystrophy; Consensus recommendations for cardiac surveillance. (2025/03/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Newborn screening and rapid genomic diagnosis of neuromuscular diseases. (2025/03/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. [Pediatric pneumological aspects in the care of children with neuromuscular diseases with focus on Duchenne muscular dystrophy]. (2025/03/01) ♡
- The N-Terminal Fragment of Urine Titin Is Not a Product of Degradation by Calpain 3. (2025/03/01) ♡
- Magnetic resonance imaging of masticatory muscles in patients with duchenne muscular dystrophy. (2025/03/01) ♡
- Stress-induced fetal programming contributes to the manifestation of Duchenne muscular dystrophy in mdx mice. (2025/03/01) ♡
- Implementation of Newborn Screening for Duchenne Muscular Dystrophy. (2025/03/01) ♡
- Cardio-metabolic and cytoskeletal proteomic signatures differentiate stress hypersensitivity in dystrophin-deficient mdx mice. (2025/02/20) ♡
- Acute Liver Injury Following Delandistrogene Moxeparvovec Gene Therapy Requiring Intravenous Immunoglobulin. (2025/02/01) ♡
- Upper body gait deviations in children with Duchenne muscular dystrophy. (2025/02/01) ♡
- Dual pH-responsive CRISPR/Cas9 ribonucleoprotein xenopeptide complexes for genome editing. (2025/02/01) ♡
- Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3-Year Study. (2025/02/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Validity and Reliability of the 6-min Pegboard and Ring Test in Patients With Duchenne Muscular Dystrophy. (2025/02/01) ♡
- Patient- and Caregiver-Reported Impact of Symptoms in Alzheimer Disease, Mild Cognitive Impairment, and Dementia. (2025/02/01) ♡
- Effect of chemical modification on the exon-skipping activity of heteroduplex oligonucleotides. (2025/02/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Facioscapulohumeral muscular dystrophy type 1 combined with becker muscular dystrophy: a family case report. (2025/01/07) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Histone deacetylase inhibition with givinostat: a multi-targeted mode of action with the potential to halt the pathological cascade of Duchenne muscular dystrophy. (2025/01/06) ♡
- The hidden face of Duchenne (Neuro)Muscular Dystrophy. Preliminary evidence of social cognition impairment as a feature of the neuropsychological phenotype of DMD. (2025/01/06) ♡
- Bone measurements interact with phenotypic measures in canine Duchenne muscular dystrophy. (2025/01/06) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. [Benefits of ω-3 fatty acids in Duchenne muscular dystrophy]. (2025/01/02) ♡
- Multi-parameter quantitative magnetic resonance imaging for early detecting skeletal muscle involvement and predicting functional decline in children with Becker muscular dystrophy. (2025/01/01) ♡
- Native DGC structure rationalizes muscular dystrophy-causing mutations. (2025/01/01) ♡
- Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohort. (2025/01/01) ♡
codex.care does not provide medical advice. Always discuss symptoms, medication, and treatment choices with your own healthcare provider.