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32,719 results on '"MUSCULAR dystrophy"'

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1. Reductions in functional muscle mass and ability to ambulate in Duchenne muscular dystrophy from ages 4 to 24 years

2. Eteplirsen Treatment for Duchenne Muscular Dystrophy: A Qualitative Patient Experience Study.

3. Benfotiamine improves dystrophic pathology and exercise capacity in mdx mice by reducing inflammation and fibrosis

4. Single-cell spatial transcriptomics reveals a dystrophic trajectory following a developmental bifurcation of myoblast cell fates in facioscapulohumeral muscular dystrophy.

5. The Development of Robust Antibodies to Sarcospan, a Dystrophin- and Integrin-Associated Protein, for Basic and Translational Research.

6. Effects of Powerchair Football: Contextual Factors That Impact Participation.

7. Engineered FSHD mutations results in D4Z4 heterochromatin disruption and feedforward DUX4 network activation

8. MCU-independent Ca2+ uptake mediates mitochondrial Ca2+ overload and necrotic cell death in a mouse model of Duchenne muscular dystrophy.

9. Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study.

10. Efficacy and Safety of Vamorolone Over 48 Weeks in Boys With Duchenne Muscular Dystrophy: A Randomized Controlled Trial.

11. Gait Characterization in Duchenne Muscular Dystrophy (DMD) Using a Single-Sensor Accelerometer: Classical Machine Learning and Deep Learning Approaches.

12. Feline dystrophin-deficient muscular dystrophy misdiagnosed as Toxoplasma myositis.

13. Meaningful changes in motor function in Duchenne muscular dystrophy (DMD): A multi-center study.

14. Functional trajectories before and after loss of ambulation in Duchenne muscular dystrophy and implications for clinical trials.

15. The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.

16. Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat.

17. Findings from the Longitudinal CINRG Becker Natural History Study.

18. Aligning with the 3Rs: alternative models for research into muscle development and inherited myopathies.

19. Cerebellar dysfunction in the mdx mouse model of Duchenne muscular dystrophy: An electrophysiological and behavioural study.

20. Muscular dystrophy as a cause of unilateral scapular winging.

21. Late‐onset primary muscle diseases mimicking sarcopenia.

22. Exploring novel natural compound-based therapies for Duchenne muscular dystrophy management: insights from network pharmacology, QSAR modeling, molecular dynamics, and free energy calculations.

23. Distinct muscle regenerative capacity of human induced pluripotent stem cell-derived mesenchymal stromal cells in Ullrich congenital muscular dystrophy model mice.

24. Challenging Diagnosis of a Patient with Two Novel Variants in the SYNE1 Gene.

25. Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype.

26. Reductions in functional muscle mass and ability to ambulate in Duchenne muscular dystrophy from ages 4 to 24 years.

27. The Hox-based positional memory in muscle stem cells.

28. Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

29. A Case Report of Becker Muscular Dystrophy and Stroke Who Successfully Regained Mobility With Robot-Assisted Gait Training.

30. Quantitative muscle magnetic resonance imaging in limb‐girdle muscular dystrophy type R1 (LGMDR1): A prospective longitudinal cohort study.

31. One‐Pot Synthesis of Orange Emissive Carbon Dots Specific for Staining of Mitochondria in both Cancer and Non‐Cancer Cells.

32. Improved diagnostic performance of high‐sensitivity cardiac troponins in muscle dystrophies using comprehensive definition criteria for cardiac involvement: A longitudinal study on 35 patients.

33. Intragenic dystrophin (DMD) duplication variant in Entlebucher Mountain Dogs with Duchenne muscular dystrophy.

34. Ameliorated cellular hallmarks of myotonic dystrophy in hybrid myotubes from patient and unaffected donor cells.

35. Muscular dystrophy patients show low exercise‐induced blood flow in muscles with normal strength.

36. Clinical and genetic evaluation of hereditary myopathies in an adult Saudi cohort.

37. Explorarea deficitelor intelectuale în distrofia musculară Duchenne și Becker.

38. A Humanized Yeast Model for Studying TRAPP Complex Mutations; Proof-of-Concept Using Variants from an Individual with a TRAPPC1 -Associated Neurodevelopmental Syndrome.

39. Genetic profile of Brazilian patients with LAMA2‐related dystrophies.

40. Three novel missense variants in two families with JAG2-associated limb-girdle muscular dystrophy.

41. AMPK as a mediator of tissue preservation: time for a shift in dogma?

42. Precision Genetic Therapies: Balancing Risk and Benefit in Patients with Heart Failure.

43. Evaluation of Dysphagia and Associated Factors in Patients with Neuromuscular Disorders: Do the Oral Factors Deserve Some Focus too?

44. The development of pGALSplus: evaluating feasibility and acceptability of an assessment to facilitate the identification and triage of children with musculoskeletal presentations.

45. Clinical Application of Optical Genome Mapping for Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy.

46. Convolutional Neural Network-Based Automated Segmentation of Skeletal Muscle and Subcutaneous Adipose Tissue on Thigh MRI in Muscular Dystrophy Patients.

47. Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy.

48. Comprehensive analysis of 2097 patients with dystrophinopathy based on a database from 2011 to 2021.

49. Bioengineered Model of Human LGMD2B Skeletal Muscle Reveals Roles of Intracellular Calcium Overload in Contractile and Metabolic Dysfunction in Dysferlinopathy.

50. Caveolin and NOS in the Development of Muscular Dystrophy.

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