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2. Treatment Decisions in Children With Asthma in a Real-Life Clinical Setting: The Swiss Paediatric Airway Cohort

5. Treatment Decisions in Children With Asthma in a Real-Life Clinical Setting: The Swiss Paediatric Airway Cohort

6. Chlamydia pneumoniae and Mycoplasma pneumoniae in children with cystic fibrosis: impact on bacterial respiratory microbiota diversity

7. Tuberculosis Disease in Children and Adolescents on Therapy With Antitumor Necrosis Factor-ɑ Agents: A Collaborative, Multicenter Paediatric Tuberculosis Network European Trials Group (ptbnet) Study

13. Hypersensitivity pneumonitis due to Pseudozyma sp. in a liver-transplanted child

14. Pneumopathie d'hypersensibilité liée à Pseudozyma chez une greffée hépatique de cinq ans

15. Pneumopathie d'hypersensibilité liée à Pseudozyma chez une greffée hépatique de cinq ans

16. Exhaled nitric oxide decreases after positive food-allergen challenge

23. Exhaled nitric oxide decreases after positive food-allergen challenge

25. Lung structural and functional impairments in young children with cystic fibrosis diagnosed following newborn screening - A nationwide observational study.

26. Data accuracy, consistency and completeness of the national Swiss cystic fibrosis patient registry: Lessons from an ECFSPR data quality project.

27. Case Report: When cystic fibrosis, elexacaftor/tezacaftor/ivacaftor therapy, and alpha1 antitrypsin deficiency get together.

28. New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome.

29. Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome.

30. Feasibility of unsedated lung MRI in young children with cystic fibrosis.

31. Determinants of lung function changes in athletic swimmers. A review.

32. Respiratory symptoms do not reflect functional impairment in early CF lung disease.

33. CFTR-function and ventilation inhomogeneity in individuals with cystic fibrosis.

34. Chlamydia pneumoniae and Mycoplasma pneumoniae in children with cystic fibrosis: impact on bacterial respiratory microbiota diversity.

36. Prevalence of tuberculosis in migrant children in Switzerland and relevance of current screening guidelines.

37. Monoacylglycerol Form of Omega-3s Improves Its Bioavailability in Humans Compared to Other Forms.

39. [Exercise induced dyspnea in adolescents].

40. Pneumocystis jirovecii Pneumonia in an Infant: The Tip of the Iceberg.

41. Alternate gas washout indices: Assessment of ventilation inhomogeneity in mild to moderate pediatric cystic fibrosis lung disease.

42. [« Doctor, my child swallowed water, can he die from dry drowning ? » An update on drowning in 2018].

43. Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls.

44. Elevated lung clearance index in infants with cystic fibrosis shortly after birth.

45. Death after cessation of treatment by cystic fibrosis patients: An international survey of clinicians.

46. Idiopathic desquamative interstitial pneumonia in a child: a case report.

47. [Former preterm infant with bronchopulmonary dysplasia: how will this be cared for in 2014?].

48. Chest CT in bronchopulmonary dysplasia: clinical and radiological correlations.

49. [Pediatrics. New treatment options for viral bronchiolitis].

50. Chest physiotherapy using passive expiratory techniques does not reduce bronchiolitis severity: a randomised controlled trial.

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