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The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial.
Tiddens HAWM, Chen Y, Andrinopoulou ER, Davis SD, Rosenfeld M, Ratjen F, Kronmal RA, Hinckley Stukovsky KD, Dasiewicz A, Stick SM; SHIP-CT Study Group. Tiddens HAWM, et al. Among authors: stick sm. Lancet Respir Med. 2022 Jul;10(7):669-678. doi: 10.1016/S2213-2600(21)00546-4. Epub 2022 Mar 11. Lancet Respir Med. 2022. PMID: 35286860 Clinical Trial.
Lung function in infants with cystic fibrosis diagnosed by newborn screening.
Linnane BM, Hall GL, Nolan G, Brennan S, Stick SM, Sly PD, Robertson CF, Robinson PJ, Franklin PJ, Turner SW, Ranganathan SC; AREST-CF. Linnane BM, et al. Among authors: stick sm. Am J Respir Crit Care Med. 2008 Dec 15;178(12):1238-44. doi: 10.1164/rccm.200804-551OC. Epub 2008 Sep 11. Am J Respir Crit Care Med. 2008. PMID: 18787217
Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening.
Sly PD, Brennan S, Gangell C, de Klerk N, Murray C, Mott L, Stick SM, Robinson PJ, Robertson CF, Ranganathan SC; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF). Sly PD, et al. Among authors: stick sm. Am J Respir Crit Care Med. 2009 Jul 15;180(2):146-52. doi: 10.1164/rccm.200901-0069OC. Epub 2009 Apr 16. Am J Respir Crit Care Med. 2009. PMID: 19372250
264 results