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3. Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6–48 months with Duchenne muscular dystrophy amenable to exon 51 skipping

4. The administration of methotrexate in patients with Still's disease, “real-life” findings from AIDA Network Still Disease Registry

5. Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6–48 months with Duchenne muscular dystrophy amenable to exon 51 skipping

6. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

7. The Administration of Methotrexate in Patients with Still's Disease, 'Real-Life' Findings from Aida Network Still Disease Registry

8. P.110 JEWELFISH: 24-month safety and pharmacodynamic data in non-treatment-naïve patients with spinal muscular atrophy (SMA)

9. Circulating endothelial progenitors are increased in COVID‐19 patients and correlate with SARS‐CoV‐2 RNA in severe cases

10. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

11. Extraperitoneal Radical Prostatectomy with the Senhance Robotic Platform: First 40 Cases

13. CLINICAL RESEARCH

14. Life expectancy in Italian patients with hereditary angioedema due to C1-inhibitor deficiency

15. Rimeporide as a first- in-class NHE-1 inhibitor : Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy

17. CLINICAL RESEARCH

18. DMD – BIOMARKERS & OUTCOME MEASURES

19. Circulating endothelial progenitors are increased in COVID‐19 patients and correlate with SARS‐CoV‐2 RNA in severe cases

20. Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy

21. Life expectancy in Italian patients with hereditary angioedema due to C1-inhibitor deficiency

22. DMD – BIOMARKERS & OUTCOME MEASURES

23. MRI – MUSCLE IMAGING

24. P.107Clinical changes over time in patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

25. P.240ASC-1 related myopathy: phenotypic spectrum and pathophysiology of an emerging congenital myopathy

26. P.107Clinical changes over time in patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

27. P.200Feasibility and baseline values of continuous movement measurement in patients with centronuclear myopathy by using ActiMyo®

28. P.240ASC-1 related myopathy: phenotypic spectrum and pathophysiology of an emerging congenital myopathy

31. OUTCOME MEASURES

32. MRI – MUSCLE IMAGING

36. Telelap Alf-X–Assisted Laparoscopy for Ovarian Cyst Enucleation: Report of the First 10 Cases

37. Congenital muscular dystrophy phenotype with neuromuscular spindles excess in a 5-year-old girl caused by HRAS mutation

38. Continuous Venovenous Hemofiltration After Coronary Procedures for the Prevention of Contrast-Induced Acute Kidney Injury in Patients With Severe Chronic Renal Failure

39. SMA THERAPIES I

40. O.28Safety and tolerability of suvodirsen (WVE-210201) in patients with Duchenne muscular dystrophy: results from a phase 1 clinical trial

41. OUTCOME MEASURES

42. Two Cases Of Peculiar Hypereosinophilic Syndrome Treated With Mepolizumab

43. Short term prophylaxis in patients with hereditary angioedema undergoing dental procedures

44. Clinical Features of Patients With Primary Angioedema With Normal Levels of C1-Inhibitor

49. SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES

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