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4. Cystic fibrosis

7. A novel thiol-saccharide mucolytic for the treatment of muco-obstructive lung diseases

11. Elexacaftor/tezacaftor/ivacaftor improves chronic rhinosinusitis detected by magnetic resonance imaging in children with cystic fibrosis on long-term therapy with lumacaftor/ivacaftor

13. Characterization of transient and progressive pulmonary fibrosis by spatially correlated phase contrast microCT, classical histopathology and atomic force microscopy

15. Advancing the pipeline of cystic fibrosis clinical trials: a new roadmap with a global trial network perspective

17. Safety and efficacy of vanzacaftor–tezacaftor–deutivacaftor in adults with cystic fibrosis: randomised, double-blind, controlled, phase 2 trials

18. Mukoviszidose

21. Contrast agent-free functional magnetic resonance imaging with matrix pencil decomposition to quantify abnormalities in lung perfusion and ventilation in patients with cystic fibrosis

25. Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

27. Comparison of the Lung Clearance Index in Preschool Children With Primary Ciliary Dyskinesia and Cystic Fibrosis

30. Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week, multicentre, randomised, double-blind, active-controlled, phase 3b trial

32. Untimely TGFβ responses in COVID-19 limit antiviral functions of NK cells

34. Reflection confocal microscopy for quantitative assessment of airway surface liquid dysregulation and pharmacological rescue in cystic fibrosis under near-physiological conditions

35. Thiolated polyglycerol sulfate as potential mucolytic for muco-obstructive lung diseases

36. Elexacaftor/tezacaftor/ivacaftor improves nasal nitric oxide in patients with cystic fibrosis

38. Multiple-breath washout to detect lung disease in patients with inborn errors of immunity

39. Pharmacological Improvement of CFTR Function Rescues Airway Epithelial Homeostasis and Host Defense in Children with Cystic Fibrosis

41. Ileal mucus viscoelastic properties differ in Crohns disease

43. Self-collected oral, nasal and saliva samples yield sensitivity comparable to professionally collected oro-nasopharyngeal swabs in SARS-CoV-2 diagnosis among symptomatic outpatients

44. COVID-19 in Pediatric Populations

45. Pharmacological Improvement of Cystic Fibrosis Transmembrane Conductance Regulator Function Rescues Airway Epithelial Homeostasis and Host Defense in Children with Cystic Fibrosis.

46. CCR3-dependent eosinophil recruitment is regulated by sialyltransferase ST3Gal-IV.

47. The future of cystic fibrosis care: a global perspective

49. Ion Mobility-Tandem Mass Spectrometry of Mucin-type O-Glycans

50. Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in People With Cystic Fibrosis and at Least OneF508delAllele: 144-Week Interim Results From a 192-Week Open-label Extension Study

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