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Thorax
|
March 23, 2011
Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF
C M Owens, P Aurora, S Stanojevic, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
October 1, 2021
Pregnancy rates and outcomes in women with cystic fibrosis in the UK: comparisons with the general population before and after the introduction of disease-modifying treatment, 2003-17
O B Esan, D K Schlüter, R Phillips, et al.
The European Respiratory Journal
|
June 1, 1997
An evaluation of two aerosol delivery systems for rhDNase
P L Shah, S F Scott, D M Geddes, et al.
Lancet (London, England)
|
December 19, 2001
Airway function in infants newly diagnosed with cystic fibrosis
S C Ranganathan, C Dezateux, A Bush, et al.
Chemical Communications (Cambridge, England)
|
May 16, 2017
Generating single metalloprotein crystals in well-defined redox states: electrochemical control combined with infrared imaging of a NiFe hydrogenase crystal
P A Ash, S B Carr, H A Reeve, et al.
Lung
|
January 26, 2018
Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index
S Irving, M Dixon, M R Fassad, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 18, 2025
Global prevalence of CFTR variants with respect to their responsiveness to elexacaftor-tezacaftor-ivacaftor
P-R Burgel, A Orenti, E Cromwell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 14, 2019
Fair selection of participants in clinical trials: The challenge to push the envelope further
J C Davies, S Scott, R Dobra, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 22, 2024
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals
E De Wachter, K De Boeck, I Sermet-Gaudelus, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Thorax
|
March 23, 2011
Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF
C M Owens, P Aurora, S Stanojevic, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
October 1, 2021
Pregnancy rates and outcomes in women with cystic fibrosis in the UK: comparisons with the general population before and after the introduction of disease-modifying treatment, 2003-17
O B Esan, D K Schlüter, R Phillips, et al.
The European Respiratory Journal
|
June 1, 1997
An evaluation of two aerosol delivery systems for rhDNase
P L Shah, S F Scott, D M Geddes, et al.
Lancet (London, England)
|
December 19, 2001
Airway function in infants newly diagnosed with cystic fibrosis
S C Ranganathan, C Dezateux, A Bush, et al.
Chemical Communications (Cambridge, England)
|
May 16, 2017
Generating single metalloprotein crystals in well-defined redox states: electrochemical control combined with infrared imaging of a NiFe hydrogenase crystal
P A Ash, S B Carr, H A Reeve, et al.
Lung
|
January 26, 2018
Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index
S Irving, M Dixon, M R Fassad, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 18, 2025
Global prevalence of CFTR variants with respect to their responsiveness to elexacaftor-tezacaftor-ivacaftor
P-R Burgel, A Orenti, E Cromwell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 14, 2019
Fair selection of participants in clinical trials: The challenge to push the envelope further
J C Davies, S Scott, R Dobra, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 22, 2024
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals
E De Wachter, K De Boeck, I Sermet-Gaudelus, et al.
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of 3