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3. Otologic features in patients with Primary Ciliary Dyskinesia- an EPIC-PCD study

5. Sinonasal features in patients with Primary Ciliary Dyskinesia - an EPIC-PCD study

7. Safety and Outcomes of Amikacin Liposome Inhalation Suspension for Mycobacterium abscessus Pulmonary Disease: A NTM-NET study

8. An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia

11. 563: Real-life initiation of elexacaftor/ivacaftor/tezacaftor in cystic fibrosis patients with severe lung disease

12. Lumacaftor/ivacaftor changes the lung microbiome and metabolome in cystic fibrosis patients

13. International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives.

14. Quality of life and psychosocial outcomes in children with severe acute asthma and their parents

19. Topological Data Analysis Coupled with Machine Learning Reveals New Genotype-Phenotype Relationships in Primary Ciliary Dyskinesia

20. Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials.

26. P047 Detection of Pseudomonas aeruginosa in exhaled breath of cystic fibrosis patients

27. Astma en het beperken van astma-exacerbaties

29. Prevalence of rhinoviruses in young children of an unselected birth cohort from the Netherlands

31. WS03.3 A phase II, randomised, double-blind, placebo-controlled, crossover study of dry powder mannitol in children with cystic fibrosis (CF)

34. 78 Combined data from two phase III studies of Bronchitol (inhaled dry powder mannitol) in adult cystic fibrosis (CF) patients

35. Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children

36. Astma en beperken van astma-exacerbaties.

38. Bcl-2 family members in childhood acute lymphoblastic leukemia: relationships with features at presentation, in vitro and in vivo drug response and long-term clinical outcome.

39. Lung function from school age to adulthood in primary ciliary dyskinesia

41. The Non-Invasive Detection of Pulmonary Exacerbations in Disorders of Mucociliary Clearance with Breath Analysis: A Systematic Review.

42. Clinical efficacy and satisfaction of a digital wheeze detector in a multicentre randomised controlled trial: the WheezeScan study.

43. Depression, anxiety, and resilience during COVID-19 in Dutch patients with cystic fibrosis or primary ciliary dyskinesia and their caregivers.

44. Axonemal structures reveal mechanoregulatory and disease mechanisms.

45. Nasal nitric oxide measurement in children for the diagnosis of primary ciliary dyskinesia: European Respiratory Society technical standard.

46. Safety and Outcomes of Amikacin Liposome Inhalation Suspension for Mycobacterium abscessus Pulmonary Disease: A NTM-NET study.

47. An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia.

49. Anxiety and depression in Dutch patients with primary ciliary dyskinesia and their caregivers: associations with health-related quality of life.

50. International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives.

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