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Becker muscular dystrophy
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Publications and studies (1748)
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Refractory atrial arrhythmias in Duchenne muscular dystrophy: a case series. (2024/08/02) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Total Laryngectomy for Respiratory Complications From Advanced Duchenne Muscular Dystrophy. (2024/08/01) ♡
- Exploring lipin1 as a promising therapeutic target for the treatment of Duchenne muscular dystrophy. (2024/07/16) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Zolpidem-triggered atrial fibrillation in a patient with cardiomyopathy: a case report. (2024/07/04) ♡
- Nutritional Issues among Children with Duchenne Muscular Dystrophy-Incidence of Deficiency and Excess Body Mass. (2024/07/04) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Social cognition in two brothers with Becker muscular dystrophy: an exploratory study revealing divergent behavioral phenotypes. (2024/07/01) ♡
- Loss of endogenous estrogen alters mitochondrial metabolism and muscle clock-related protein Rbm20 in female mdx mice. (2024/06/15) ♡
- Persistent inflammation and nutritional status in Duchenne muscular dystrophy. (2024/06/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. GDE5/Gpcpd1 activity determines phosphatidylcholine composition in skeletal muscle and regulates contractile force in mice. (2024/05/20) ♡
- Diversity of mutations in the dystrophin gene and details of muscular lesions in porcine dystrophinopathies. (2024/05/01) ♡
- 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. Regenerative inflammation: When immune cells help to re-build tissues. (2024/04/01) ♡
- Cognitive abnormalities in Becker muscular dystrophy: a mysterious link between dystrophin deficiency and executive functions. (2024/04/01) ♡
- 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. Long-term safety and efficacy of cipaglucosidase alfa plus miglustat in individuals living with Pompe disease: an open-label phase I/II study (ATB200-02). (2024/04/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. The slow-release adiponectin analog ALY688-SR modifies early-stage disease development in the D2.mdx mouse model of Duchenne muscular dystrophy. (2024/04/01) ♡
- "I don't know whether I will be alive or not" - An interpretative phenomenological analysis of young adult males with Duchenne Muscular Dystrophy making sense of self and life. (2024/04/01) ♡
- Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy. (2024/04/01) ♡
- Pilot study of a virtual weight management program for Duchenne muscular dystrophy. (2024/04/01) ♡
- 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. The unconditioned fear response in vertebrates deficient in dystrophin. (2024/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Pragmatic Neurorehabilitation Approach for Improving Quality of Life in Duchenne Muscular Dystrophy: A Case Report. (2024/03/17) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Deep-seated dermatophytosis caused by Trichophyton rubrum in patient with Becker muscular dystrophy. (2024/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Late-onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles. (2024/03/01) ♡
- Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Family Involvement and at-Home Physical Therapy on Duchenne Muscular Dystrophy: A Randomized Controlled Trial. (2024/03/01) ♡
- Management and Outcomes of Femur Fractures in Patients with Duchenne Muscular Dystrophy. (2024/02/12) ♡
- 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. Applications of Gene Therapy in Cardiomyopathies. (2024/02/01) ♡
- Meeting report: The 2023 FSHD International Research Congress. (2024/02/01) ♡
- Insight into the Role of Gut Microbiota in Duchenne Muscular Dystrophy: An Age-Related Study in Mdx Mice. (2024/02/01) ♡
- Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. The ALPHA phase 1 study: pulmonary ArteriaL hypertension treated with CardiosPHere-Derived allogeneic stem cells. (2024/02/01) ♡
- 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. Targeted genetic therapies for inherited disorders that affect both cardiac and skeletal muscle. (2024/02/01) ♡
- Mechanisms of reduced myocardial energetics of the dystrophic heart. (2024/02/01) ♡
- Empagliflozin treatment rescues abnormally reduced Na(+) currents in ventricular cardiomyocytes from dystrophin-deficient mdx mice. (2024/02/01) ♡
- Self- and Caregiver-Reported Participation, Quality of Life, and Related Mood and Behavior Challenges in People Living With Dystrophinopathies. (2024/02/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model. (2024/02/01) ♡
- A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data. (2024/02/01) ♡
- Dual task impact on functional mobility and interaction of functional level and balance in patients with Duchenne muscular dystrophy. (2024/02/01) ♡
- Neurodiversity, treatment compliance and survival in adults with Duchenne muscular dystrophy: a single-centre retrospective cohort review. (2024/02/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy. (2024/02/01) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of the Evidence. (2024/01/23) ♡
- 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. Neuromuscular disorders in the omics era. (2024/01/15) ♡
- 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. DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis. (2024/01/15) ♡
- Clinical practice guidelines for the diagnosis and management of Duchenne muscular dystrophy: a scoping review. (2024/01/05) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy. (2024/01/01) ♡
- Developing a Natural History Model for Duchenne Muscular Dystrophy. (2024/01/01) ♡
- Antioxidant effects of LEDT in dystrophic muscle cells: involvement of PGC-1α and UCP-3 pathways. (2024/01/01) ♡
- Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting. (2024/01/01) ♡
- Prevalence of Adeno-Associated Virus-9-Neutralizing Antibody in Chinese Patients with Duchenne Muscular Dystrophy. (2024/01/01) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Fat embolism syndrome in Duchenne muscular dystrophy: Report on a novel case and systematic literature review. (2024/01/01) ♡
- The Interaction of Duchenne Muscular Dystrophy and Insulin Resistance. (2024/01/01) ♡
- Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study. (2024/01/01) ♡
- Evaluation of pro-regenerative and anti-inflammatory effects of isolecanoric acid in the muscle: Potential treatment of Duchenne Muscular Dystrophy. (2024/01/01) ♡
- Understanding anxiety experienced by young males with Duchenne muscular dystrophy: a qualitative focus group study. (2024/01/01) ♡
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