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1. Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial

2. Effects of mexiletine on hyperexcitability in sporadic amyotrophic lateral sclerosis: Preliminary findings from a small phase II randomized controlled trial

3. Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies

4. Lean tissue mass measurements by dual-energy X-ray absorptiometry and associations with strength and functional outcome measures in facioscapulohumeral muscular dystrophy

6. Defining SOD1 ALS natural history to guide therapeutic clinical trial design

12. Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progression.

16. Validation of the association between MRI and gene signatures in facioscapulohumeral dystrophy muscle: implications for clinical trial design

20. Quantitative muscle analysis in facioscapulohumeral muscular dystrophy using whole‐body fat‐referenced MRI : Protocol development, multicenter feasibility, and repeatability

21. Quantitative muscle analysis in facioscapulohumeral muscular dystrophy using whole-body fat-referenced MRI: Protocol development, multicenter feasibility, and repeatability

23. Contributors

27. Additional file 4 of Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy

30. Contributors

31. Myositis associated anti-NT5C1A autoantibody in clinical practice

34. Colaboradores

38. List of Contributors

39. MRI-informed muscle biopsies correlate MRI with pathology and DUX4 target gene expression in FSHD

45. Death with dignity in Washington patients with amyotrophic lateral sclerosis

48. Defining SOD1 ALS natural history to guide therapeutic clinical trial design

50. List of Contributors

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