Inhaled alpha 1 -proteinase inhibitor therapy in patients with cystic fibrosis
Amit Gaggar(University of Alabama at Birmingham), Scott H. Donaldson(University of North Carolina at Chapel Hill), Henry L. Dorkin(Boston Children's Hospital), Rhonda Griffin(Grifols (United States)), James F. Chmiel(Riley Hospital for Children), Patrick A. Flume(Medical University of South Carolina), Junliang Chen(Sun Yat-sen University), David P. Nichols(Cystic Fibrosis Foundation)
Cited by 57
Related Papers
Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del<i>CFTR</i>
|New England Journal of Medicine|2015|1.6k
Randomized Trial of Omalizumab (Anti-IgE) for Asthma in Inner-City Children
|New England Journal of Medicine|2011|870
Effect of VX-770 in Persons with Cystic Fibrosis and the G551D- <i>CFTR</i> Mutation
|New England Journal of Medicine|2010|802
Efficacy of Aerosolized Tobramycin in Patients with Cystic Fibrosis
|New England Journal of Medicine|1993|458