The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial

Pulmonary FibrosisBronchi

Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography

Pediatr Pulmonol.

Kuo W, Soffers T, Andrinopoulou ER, Rosenow T, Ranganathan S, Turkovic L, Stick SM, Tiddens HAWM; AREST CF

doi: 10.1002/ppul.23787.

Pulmonary Fibrosis

The Changing Prevalence of Lower Airway Infections in Young Children with Cystic Fibrosis

Thorax.

Breuer O, Schultz A, Turkovic L, de Klerk N, Keil AD, Brennan S, Harrison J, Robertson C, Robinson PJ, Sly PD, Ranganathan S, Stick SM, Caudri D; AREST CF

doi: 10.1136/

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Further Publications

Effects of a Partially Supervised Conditioning Program in Cystic Fibrosis: An International Multicenter Randomized Controlled Trial (ACTIVATE-CF)

★ 2 Recommended by Dr Martin Frey, Faculty Member

Am J Respir Crit Care Med

Hebestreit H, Kriemler S, Schindler C, Stein L, Karila C, Urquhart DS, Orenstein DM, Lands LC, Schaeff J, Eber E, Radtke T, ACTIVATE-CF Study Working Group.

doi: 10.1164/rccm.202106-1419OC

Fungal and Bacterial Diversity of Airway Microbiota in Adults with Cystic Fibrosis: Concordance Between Conventional Methods and Ultra-Deep Sequencing, and Their Practical use in the Clinical Laboratory

Mycopathologia.

Botterel F, Angebault C, Cabaret O, Stressmann FA, Costa JM, Wallet F, Wallaert B, Bruce K, Delhaes L

doi: 10.1007/s11046-017-0185-x.

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

PLoS Pathog.

Muhlebach MS, Zorn BT, Esther CR, Hatch JE, Murray CP, Turkovic L, Ranganathan SC, Boucher RC, Stick SM, Wolfgang MC

doi: 10.1371/

COMMENTED

Inhaled mannitol for cystic fibrosis

Cochrane Database Syst Rev.

Nevitt SJ, Thornton J, Murray CS, Dwyer T

doi: 10.1002/14651858.

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Pulmonary Fibrosis

Assessment of early lung disease in young children with CF: A comparison between pressure-controlled and free-breathing chest computed tomography

★ 1 Recommended by Dr Martin Frey, Faculty Member

★ 2 Recommended by Dr Marcus Hesse, Faculty Member

Pediatr Pulmonol.

Oudraad MCJ, Kuo W, Rosenow T, Andrinopoulou ER, Stick SM, Tiddens HAWM

doi: 10.1002/ppul.24702.

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Pulmonary Fibrosis

Inhaled hypertonic saline in preschool children with cystic fibrosis (SHIP): a multicentre, randomised, double-blind, placebo-controlled trial

Lancet Respir Med.

Ratjen F, Davis SD, Stanojevic S, Kronmal RA, Hinckley Stukovsky KD, Jorgensen N, Rosenfeld M, SHIP Study Group.

doi: 10.1016/S2213-

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Pulmonary Fibrosis

Sputum versus nasopharyngeal samples for the molecular diagnosis of respiratory viral infection in cystic fibrosis: A pilot study

★ 2 Recommended by Dr Martin Frey, Faculty Member

J Cyst Fibros.

Cardot-Martin E, Guillou-Guillemette HL, Berre RL, Ramel S, Bihan JL, Grenet D, Farfour E, Troussier F, Urban T, Billard L, Pilorgé L, Minoui-Tran A, Payan C, Munck MR, Héry-Arnaud G, Vallet S

doi: 10.1016/j.jcf.2020.09.003.

Related content

Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography

The Changing Prevalence of Lower Airway Infections in Young Children with Cystic Fibrosis

Effects of a Partially Supervised Conditioning Program in Cystic Fibrosis: An International Multicenter Randomized Controlled Trial (ACTIVATE-CF)

Fungal and Bacterial Diversity of Airway Microbiota in Adults with Cystic Fibrosis: Concordance Between Conventional Methods and Ultra-Deep Sequencing, and Their Practical use in the Clinical Laboratory

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

Inhaled mannitol for cystic fibrosis

Assessment of early lung disease in young children with CF: A comparison between pressure-controlled and free-breathing chest computed tomography

Inhaled hypertonic saline in preschool children with cystic fibrosis (SHIP): a multicentre, randomised, double-blind, placebo-controlled trial

Sputum versus nasopharyngeal samples for the molecular diagnosis of respiratory viral infection in cystic fibrosis: A pilot study