Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study-Reference-Cited by-同舟云学术

Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study

Published:2018-07 Issue:7 Volume:6 Page:545-553
ISSN:2213-2600
Container-title:The Lancet Respiratory Medicine
language:en
Short-container-title:The Lancet Respiratory Medicine

Author:

Rosenfeld Margaret,Wainwright Claire E,Higgins Mark,Wang Linda T,McKee Charlotte,Campbell Daniel,Tian Simon,Schneider Jennifer,Cunningham Steve,Davies Jane C,Rosenfeld Margaret,Wainwright Claire E.,Higgins Mark,Wang Linda T.,McKee Charlotte,Campbell Daniel,Tian Simon,Schneider Jennifer,Cunningham Steve,Davies Jane C.,Harris William,Mogayzel Peter,McCoy Karen,Milla Carlos,Rubenstein Ronald,Walker Seth,Black Philip,Montgomery Gregory,McColley Susanna,Hiatt Peter,Sawicki Gregory,Rock Michael,Aurora Paul,Ratjen Felix,Maitra Anirban,Ives Andrew,Gaillard Erol,McNalley Paul,Selvadurai Hiranjan,Robinson Philip

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine

Reference21 articles.

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5. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT;Mott;Thorax,2012

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