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336 results on '"Karaa, Amel"'

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1. Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study.

2. Genotype-specific effects of elamipretide in patients with primary mitochondrial myopathy: a post hoc analysis of the MMPOWER-3 trial

3. Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.

4. Prolonged Hypoxic Breathing in Healthy Volunteers: a Safety Study (MGH-nitrogen)

8. Clinical outcomes among young patients with Fabry disease who initiated agalsidase beta treatment before 30 years of age: An analysis from the Fabry Registry

11. Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey.

12. Analysis of the baseline characteristics of Fabry disease patients screened for the pegunigalsidase alfa phase III BALANCE study

14. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

15. Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project

22. Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study

23. Phenotypes of undiagnosed adults with actionable OTC and GLA variants

24. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

25. Mitochondrial diseases in North America: An analysis of the NAMDC Registry

27. Nutritional interventions in primary mitochondrial disorders: Developing an evidence base

31. Clinical outcomes among young patients with Fabry disease who initiated agalsidase beta treatment before 30 years of age:An analysis from the Fabry Registry

32. Efficacy and Safety of Elamipretide in Individuals with Primary Mitochondrial Myopathy:The MMPOWER-3 Randomized Clinical Trial

33. Clinical trials in mitochondrial diseases

37. Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial.

38. Linear IGA bullous dermatosis in Tunisian children : 31 cases

40. Response to Newman et al.

42. Community Consensus Guidelines to Support FAIR Data Standards in Clinical Research Studies in Primary Mitochondrial Disease

43. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

46. Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensus

47. Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells

48. Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project

50. Thromboxane [A.sub.2] from Kupffer cells contributes to the hyperresponsiveness of hepatic portal circulation to endothelin-1 in endotoxemic rats

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