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Duchenne muscular dystrophy

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchHighest level of evidence only (36)Meta-analysis (9)Randomized trial (11)Systematic review (9)Phase 3 study (7)Clinical examination (506)Review article (205)Early study (phase 1 or 2) (27)Case report (101)Laboratory or animal study (64)Commentary or editorial (52)Retracted Publication (4) Studies Currently Seeking Participants Only (38)

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Publications (1250)

• Identification of reference microRNAs in skeletal muscle of a canine model of Duchenne muscular dystrophy. (2024/11/20) ♡
• DMD mutations in pediatric patients with phenotypes of Duchenne/Becker muscular dystrophy. (2024/11/15) ♡
• Duchenne muscular dystrophy patients diagnosed at the asymptomatic stage: What are the benefits of early diagnosis? (2024/11/14) ♡
• Lipin1 as a therapeutic target for respiratory insufficiency of duchenne muscular dystrophy. (2024/11/12) ♡
• Epigenetic control of myogenic identity of human muscle stem cells in Duchenne muscular dystrophy. (2024/11/08) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene. (2024/11/06) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. In Vitro Gene Therapy Using Human iPS-Derived Mesoangioblast-Like Cells (HIDEMs) Combined with Microdystrophin (μDys) Expression as the New Strategy for Duchenne Muscular Dystrophy (DMD) Experimental Treatment. (2024/11/05) ♡
• Long-term course of gastrostomy nutritional management in patients with Duchenne muscular dystrophy: A retrospective cohort study. (2024/11/01) ♡
• Gross motor delays in infants and young boys with Duchenne muscular dystrophy. (2024/11/01) ♡
• An Exoskeleton Design and Numerical Characterization for Children with Duchenne Muscular Dystrophy. (2024/10/26) ♡
• Utilization of Multi-Parametric Quantitative Magnetic Resonance Imaging in the Early Diagnosis of Duchenne Muscular Dystrophy. (2024/10/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Editorial for "Utilization of Multi-Parametric Quantitative Magnetic Resonance Imaging in the Early Diagnosis of Duchenne Muscular Dystrophy". (2024/10/01) ♡
• 274th ENMC international workshop: recommendations for optimizing bone strength in neuromuscular disorders. Hoofddorp, The Netherlands, 19-21 January 2024. (2024/10/01) ♡
• Mitohormesis during advanced stages of Duchenne muscular dystrophy reveals a redox-sensitive creatine pathway that can be enhanced by the mitochondrial-targeting peptide SBT-20. (2024/10/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Reductions in functional muscle mass and ability to ambulate in Duchenne muscular dystrophy from ages 4 to 24 years. (2024/10/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Effect of Oral Zinc Supplementation on Phase Angle and Bioelectrical Impedance Vector Analysis in Duchenne Muscular Dystrophy: A Non-Randomized Clinical Trial. (2024/09/29) ♡
• Effect of Zinc Supplementation on Body Composition of Duchenne Muscular Dystrophy Patients: A Quasi-Experimental Study. (2024/09/18) ♡
• Sexual health and fertility in Duchenne muscular dystrophy—An exploratory study. (2024/09/01) ♡
• 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. Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience. (2024/09/01) ♡
• Comprehensive analysis of 2097 patients with dystrophinopathy based on a database from 2011 to 2021. (2024/08/24) ♡
• Unveiling the Respiratory Muscle Strength in Duchenne Muscular Dystrophy: The Impact of Nutrition and Thoracic Deformities, Beyond Spirometry. (2024/08/15) ♡
• 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. Caveolin and NOS in the Development of Muscular Dystrophy. (2024/08/12) ♡
• 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) ♡
• 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. Isolated cardiomyopathy in a pathogenic X-linked in frame hemizygous DMD exon 49 deletion: A rare presentation with normal creatine kinase levels and absence of musculoskeletal symptoms. (2024/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. 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) ♡

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