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Page 1
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.
Konstan MW, Morgan WJ, Butler SM, Pasta DJ, Craib ML, Silva SJ, Stokes DC, Wohl ME, Wagener JS, Regelmann WE, Johnson CA; Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Konstan MW, et al. Among authors: craib ml. J Pediatr. 2007 Aug;151(2):134-9, 139.e1. doi: 10.1016/j.jpeds.2007.03.006. Epub 2007 Jun 22. J Pediatr. 2007. PMID: 17643762
Risk factors for mortality before age 18 years in cystic fibrosis.
McColley SA, Schechter MS, Morgan WJ, Pasta DJ, Craib ML, Konstan MW. McColley SA, et al. Among authors: craib ml. Pediatr Pulmonol. 2017 Jul;52(7):909-915. doi: 10.1002/ppul.23715. Epub 2017 Apr 24. Pediatr Pulmonol. 2017. PMID: 28436621
Cystic fibrosis clinical characteristics associated with dornase alfa treatment regimen change.
VanDevanter DR, Craib ML, Pasta DJ, Millar SJ, Morgan WJ, Konstan MW; Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. VanDevanter DR, et al. Among authors: craib ml. Pediatr Pulmonol. 2018 Jan;53(1):43-49. doi: 10.1002/ppul.23897. Epub 2017 Oct 24. Pediatr Pulmonol. 2018. PMID: 29064184