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3. Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy

4. Transition

7. Klinische Befunde

11. Myasthenia gravis

13. Dermatomyositis

21. Correction to: Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study (Neurology and Therapy, (2023), 12, 2, (543-557), 10.1007/s40120-023-00444-1)

22. Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy

23. Real-World Data on the Efficacy of Gene Replacement Therapy for Spinal Muscular Atrophy (SMA).

25. Einleitung

28. O.13 Givinostat in DMD: results of the Epidys Study

29. P.83 Molecular pathology of human PPP1R21 deficiency

32. Ataluren delays loss of ambulation and respiratory decline in nonsense mutation Duchenne muscular dystrophy patients

34. Labor

36. Genetik

37. Deflazacort vs prednisone treatment for Duchenne muscular dystrophy: A meta‐analysis of disease progression rates in recent multicenter clinical trials

46. Klinische Befunde

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