Determinants of lung disease progression measured by lung clearance index in children with cystic fibrosis

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Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth

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Korten I, Kieninger E, Yammine S, Cangiano G, Nyilas S, Anagnostopoulou P, Singer F, Kuehni CE, Regamey N, Frey U, Casaulta C, Spycher BD, Latzin P; SCILD; BILD study group

doi: 10.1016/j.jcf.2018.07.002.

Lung clearance index to monitor treatment response in pulmonary exacerbations in preschool children with cystic fibrosis

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Rayment JH, Stanojevic S, Davis SD, Retsch-Bogart G, Ratjen F

doi: 10.1136/

Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children

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doi: 10.1371/

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Am J Respir Crit Care Med.

Perrem L, Stanojevic S, Shaw M, Jensen R, McDonald N, Isaac SM, Davis M, Clem C, Guido J, Jara S, France L, Solomon M, Grasemann H, Waters V, Sweezey N, Sanders DB, Davis SD, Ratjen F

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