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Pediatrics
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October 14, 2017
False-Positive Newborn Screening for Cystic Fibrosis and Health Care Use
Robin Z Hayeems, Fiona A Miller, Marian Vermeulen, et al.
ERJ Open Research
|
March 18, 2026
Utility of hyperpolarised xenon-129 magnetic resonance imaging in primary ciliary dyskinesia
Wallace B Wee, Brandon Zanette, Samal Munidasa, et al.
The Lancet. Respiratory Medicine
|
June 14, 2017
Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial
Felix Ratjen, Christopher Hug, Gautham Marigowda, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
June 14, 2014
Lung arginase expression and activity is increased in cystic fibrosis mouse models
Thomas Jaecklin, Julia Duerr, Hailu Huang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 13, 2015
Alternative outcomes for the multiple breath washout in children with CF
Sanja Stanojevic, Renee Jensen, Dasiga Sundaralingam, et al.
The Lancet. Respiratory Medicine
|
May 9, 2021
Long-term safety of lumacaftor-ivacaftor in children aged 2-5 years with cystic fibrosis homozygous for the F508del-CFTR mutation: a multicentre, phase 3, open-label, extension study
Jordana E Hoppe, Mark Chilvers, Felix Ratjen, et al.
Pediatric Neurology
|
February 17, 2022
Neurovascular Manifestations in Pediatric Patients With Hereditary Haemorrhagic Telangiectasia
Roxana Azma, Adam A Dmytriw, Asthik Biswas, et al.
Chest
|
May 19, 2012
Effect of azithromycin on systemic markers of inflammation in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa
Felix Ratjen, Lisa Saiman, Nicole Mayer-Hamblett, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 14, 2013
Pulmonary exacerbations in CF patients with early lung disease
Michael Anstead, Lisa Saiman, Nicole Mayer-Hamblett, et al.
The Journal of Pediatrics
|
December 27, 2011
Utility of contrast echocardiography for pulmonary arteriovenous malformation screening in pediatric hereditary hemorrhagic telangiectasia
Suhail Al-Saleh, Andreea Dragulescu, David Manson, et al.
Page
of 33
Search research articles
Search
Showing results (211-220 of 326) with videos related to
Sort By:
Page
of 33
Pediatrics
|
October 14, 2017
False-Positive Newborn Screening for Cystic Fibrosis and Health Care Use
Robin Z Hayeems, Fiona A Miller, Marian Vermeulen, et al.
ERJ Open Research
|
March 18, 2026
Utility of hyperpolarised xenon-129 magnetic resonance imaging in primary ciliary dyskinesia
Wallace B Wee, Brandon Zanette, Samal Munidasa, et al.
The Lancet. Respiratory Medicine
|
June 14, 2017
Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial
Felix Ratjen, Christopher Hug, Gautham Marigowda, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
June 14, 2014
Lung arginase expression and activity is increased in cystic fibrosis mouse models
Thomas Jaecklin, Julia Duerr, Hailu Huang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 13, 2015
Alternative outcomes for the multiple breath washout in children with CF
Sanja Stanojevic, Renee Jensen, Dasiga Sundaralingam, et al.
The Lancet. Respiratory Medicine
|
May 9, 2021
Long-term safety of lumacaftor-ivacaftor in children aged 2-5 years with cystic fibrosis homozygous for the F508del-CFTR mutation: a multicentre, phase 3, open-label, extension study
Jordana E Hoppe, Mark Chilvers, Felix Ratjen, et al.
Pediatric Neurology
|
February 17, 2022
Neurovascular Manifestations in Pediatric Patients With Hereditary Haemorrhagic Telangiectasia
Roxana Azma, Adam A Dmytriw, Asthik Biswas, et al.
Chest
|
May 19, 2012
Effect of azithromycin on systemic markers of inflammation in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa
Felix Ratjen, Lisa Saiman, Nicole Mayer-Hamblett, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 14, 2013
Pulmonary exacerbations in CF patients with early lung disease
Michael Anstead, Lisa Saiman, Nicole Mayer-Hamblett, et al.
The Journal of Pediatrics
|
December 27, 2011
Utility of contrast echocardiography for pulmonary arteriovenous malformation screening in pediatric hereditary hemorrhagic telangiectasia
Suhail Al-Saleh, Andreea Dragulescu, David Manson, et al.
Page
of 33