43 results on '"McDonald, Craig M."'
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2. Practical Considerations for Delandistrogene Moxeparvovec Gene Therapy in Patients With Duchenne Muscular Dystrophy
3. Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial
4. Influence of β2 adrenergic receptor genotype on longitudinal measures of forced vital capacity in patients with Duchenne muscular dystrophy
5. Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy
6. Rasch Analysis of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales Administered to Patients With Duchenne Muscular Dystrophy
7. Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study
8. Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
9. Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy
10. Efficacy of idebenone on respiratory function in patients with Duchenne muscular dystrophy not using glucocorticoids (DELOS): a double-blind randomised placebo-controlled phase 3 trial
11. Evaluation of Phrenic Nerve and Diaphragm Function with Peripheral Nerve Stimulation and M-Mode Ultrasonography in Potential Pediatric Phrenic Nerve or Diaphragm Pacing Candidates
12. Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
13. Management of Pulmonary Complications in Neuromuscular Disease
14. Treatment of Spine Deformity in Neuromuscular Diseases
15. Mobility-Assistive Technology in Progressive Neuromuscular Disease
16. Clinical Approach to the Diagnostic Evaluation of Hereditary and Acquired Neuromuscular Diseases
17. Prevention and Management of Limb Contractures in Neuromuscular Diseases
18. The Role of the Neuromuscular Medicine and Physiatry Specialists in the Multidisciplinary Management of Neuromuscular Disease
19. Exercise in Neuromuscular Diseases
20. Regional and Whole-Body Dual-Energy X-Ray Absorptiometry to Guide Treatment and Monitor Disease Progression in Neuromuscular Disease
21. 42 - Trastornos miopáticos
22. 42 - Myopathic Disorders
23. Diagnosis and Clinical Management of Spinal Muscular Atrophy
24. The relationship between regional body composition and quantitative strength in facioscapulohumeral muscular dystrophy (FSHD)
25. Change in Life Satisfaction of Adults With Pediatric-Onset Spinal Cord Injury
26. Pain in Persons With Postpolio Syndrome: Frequency, Intensity, and Impact
27. Chronic Pain in Persons With Myotonic Dystrophy and Facioscapulohumeral Dystrophy
28. Chronic Pain in Persons With Neuromuscular Disease
29. Use of step activity monitoring for continuous physical activity assessment in boys with Duchenne muscular dystrophy
30. Utility of a step activity monitor for the measurement of daily ambulatory activity in children
31. Evidence-based care in Duchenne muscular dystrophy
32. Colaboradores
33. Peripheral Neuropathies of Childhood
34. Contributors
35. William M. Fowler, Jr, MD, 1926-2017
36. Convexity of Scoliosis Related to Handedness in Identical Twin Boys With Duchenne's Muscular Dystrophy: A Case Report
37. Neuromuscular Disease Management and Rehabilitation, Part II: Specialty Care and Therapeutics
38. Neuromuscular Disease Management and Rehabilitation, Part I: Diagnostic and Therapy Issues
39. Pain in Myotonic Muscular Dystrophy, Type 1
40. Dedication
41. Urodynamic Findings in the Tethered Spinal Cord Syndrome: Does Surgical Release Improve Bladder Function?
42. Chapter 48 - Myopathic Disorders
43. Contributors
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