Controlled longitudinal study of bone mass accrual in children and adolescents with cystic fibrosis

Por Buntain, H M, Schluter, P J, Bell, S C, Greer, R M, Wong, J C H, Batch, J, Lewindon, P, Wainwright, C E
Publicado em 2006

Cough-generated aerosols of Pseudomonas aeruginosa and other Gram-negative bacteria from patients with cystic fibrosis

Por Wainwright, C E, France, M W, O’Rourke, P, Anuj, S, Kidd, T J, Nissen, M D, Sloots, T P, Coulter, C, Ristovski, Z, Hargreaves, M, Rose, B R, Harbour, C, Bell, S C, Fennelly, K P
Publicado em 2009

Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR

Por Wainwright, C.E., Elborn, J.S., Ramsey, B.W., Marigowda, G., Huang, X., Cipolli, M., Colombo, C., Davies, J.C., De Boeck, K., Flume, P.A., Konstan, M.W., McColley, S.A., McCoy, K., McKone, E.F., Munck, A., Ratjen, F., Rowe, S.M., Waltz, D., Boyle, M.P.
Publicado no N Engl J Med (2015)