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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 25, 2018
The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF
Paul D W Eckford, Jacqueline McCormack, Lise Munsie, et al.
The European Respiratory Journal
|
February 12, 2013
Consensus statement for inert gas washout measurement using multiple- and single- breath tests
Paul D Robinson, Philipp Latzin, Sylvia Verbanck, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 24, 2022
Elexacaftor/tezacaftor/ivacaftor and gastrointestinal outcomes in cystic fibrosis: Report of promise-GI
Sarah Jane Schwarzenberg, Phuong T Vu, Michelle Skalland, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
March 7, 2018
ECFS best practice guidelines: the 2018 revision
Carlo Castellani, Alistair J A Duff, Scott C Bell, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 11, 2022
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for <i>F508del</i> and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study
Marcus A Mall, Rossa Brugha, Silvia Gartner, et al.
The Lancet. Respiratory Medicine
|
November 7, 2022
Discontinuation versus continuation of hypertonic saline or dornase alfa in modulator treated people with cystic fibrosis (SIMPLIFY): results from two parallel, multicentre, open-label, randomised, controlled, non-inferiority trials
Nicole Mayer-Hamblett, Felix Ratjen, Renee Russell, et al.
Pediatrics
|
November 23, 2021
Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age
Tanja Gonska, Katherine Keenan, Jacky Au, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 16, 2021
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial
David P Nichols, Alex C Paynter, Sonya L Heltshe, et al.
The Lancet. Respiratory Medicine
|
September 12, 2023
Advancing the pipeline of cystic fibrosis clinical trials: a new roadmap with a global trial network perspective
Nicole Mayer-Hamblett, John Paul Clancy, Raksha Jain, et al.
HGG Advances
|
November 17, 2022
High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
Scott Mastromatteo, Angela Chen, Jiafen Gong, et al.
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of 33
Search research articles
Search
Showing results (311-320 of 326) with videos related to
Sort By:
Page
of 33
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 25, 2018
The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF
Paul D W Eckford, Jacqueline McCormack, Lise Munsie, et al.
The European Respiratory Journal
|
February 12, 2013
Consensus statement for inert gas washout measurement using multiple- and single- breath tests
Paul D Robinson, Philipp Latzin, Sylvia Verbanck, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 24, 2022
Elexacaftor/tezacaftor/ivacaftor and gastrointestinal outcomes in cystic fibrosis: Report of promise-GI
Sarah Jane Schwarzenberg, Phuong T Vu, Michelle Skalland, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
March 7, 2018
ECFS best practice guidelines: the 2018 revision
Carlo Castellani, Alistair J A Duff, Scott C Bell, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 11, 2022
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for <i>F508del</i> and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study
Marcus A Mall, Rossa Brugha, Silvia Gartner, et al.
The Lancet. Respiratory Medicine
|
November 7, 2022
Discontinuation versus continuation of hypertonic saline or dornase alfa in modulator treated people with cystic fibrosis (SIMPLIFY): results from two parallel, multicentre, open-label, randomised, controlled, non-inferiority trials
Nicole Mayer-Hamblett, Felix Ratjen, Renee Russell, et al.
Pediatrics
|
November 23, 2021
Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age
Tanja Gonska, Katherine Keenan, Jacky Au, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 16, 2021
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial
David P Nichols, Alex C Paynter, Sonya L Heltshe, et al.
The Lancet. Respiratory Medicine
|
September 12, 2023
Advancing the pipeline of cystic fibrosis clinical trials: a new roadmap with a global trial network perspective
Nicole Mayer-Hamblett, John Paul Clancy, Raksha Jain, et al.
HGG Advances
|
November 17, 2022
High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
Scott Mastromatteo, Angela Chen, Jiafen Gong, et al.
Page
of 33