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BMC Infectious Diseases
|
December 5, 2014
Urine lipoarabinomannan point-of-care testing in patients affected by pulmonary nontuberculous mycobacteria--experiences from the Danish Cystic Fibrosis cohort study
Tavs Qvist, Isik S Johansen, Tania Pressler, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
November 21, 2018
The importance of early diagnosis of Mycobacterium abscessus complex in patients with cystic fibrosis
Cecilie Ravnholt, Mette Kolpen, Marianne Skov, et al.
Thorax
|
May 5, 2012
Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study
David Taylor-Robinson, Margaret Whitehead, Finn Diderichsen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 23, 2018
Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations
Tavs Qvist, Daniela K Schlüter, Vian Rajabzadeh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 22, 2016
Phenotypic shift in Pseudomonas aeruginosa populations from cystic fibrosis lungs after 2-week antipseudomonal treatment
Laia Fernández-Barat, Oana Ciofu, Kasper N Kragh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 15, 2006
Autoantibody response to BPI predict disease severity and outcome in cystic fibrosis
Malin Carlsson, Leif Eriksson, Tania Pressler, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 19, 2012
Colonisation and infection of the paranasal sinuses in cystic fibrosis patients is accompanied by a reduced PMN response
Helle Krogh Johansen, Kasper Aanaes, Tania Pressler, et al.
Journal of Clinical Medicine
|
April 3, 2021
Bacterial Re-Colonization Occurs Early after Lung Transplantation in Cystic Fibrosis Patients
Anna Engell Holm, Hans Henrik Lawaetz Schultz, Helle Krogh Johansen, et al.
The European Respiratory Journal
|
September 5, 2014
Low socioeconomic status is associated with worse lung function in the Danish cystic fibrosis population
David C Taylor-Robinson, Karsten Thielen, Tania Pressler, et al.
Pediatric Pulmonology
|
November 5, 2019
Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years
Marianne Skov, Marie Baekvad-Hansen, David M Hougaard, et al.
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Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
BMC Infectious Diseases
|
December 5, 2014
Urine lipoarabinomannan point-of-care testing in patients affected by pulmonary nontuberculous mycobacteria--experiences from the Danish Cystic Fibrosis cohort study
Tavs Qvist, Isik S Johansen, Tania Pressler, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
November 21, 2018
The importance of early diagnosis of Mycobacterium abscessus complex in patients with cystic fibrosis
Cecilie Ravnholt, Mette Kolpen, Marianne Skov, et al.
Thorax
|
May 5, 2012
Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study
David Taylor-Robinson, Margaret Whitehead, Finn Diderichsen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 23, 2018
Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations
Tavs Qvist, Daniela K Schlüter, Vian Rajabzadeh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 22, 2016
Phenotypic shift in Pseudomonas aeruginosa populations from cystic fibrosis lungs after 2-week antipseudomonal treatment
Laia Fernández-Barat, Oana Ciofu, Kasper N Kragh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 15, 2006
Autoantibody response to BPI predict disease severity and outcome in cystic fibrosis
Malin Carlsson, Leif Eriksson, Tania Pressler, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 19, 2012
Colonisation and infection of the paranasal sinuses in cystic fibrosis patients is accompanied by a reduced PMN response
Helle Krogh Johansen, Kasper Aanaes, Tania Pressler, et al.
Journal of Clinical Medicine
|
April 3, 2021
Bacterial Re-Colonization Occurs Early after Lung Transplantation in Cystic Fibrosis Patients
Anna Engell Holm, Hans Henrik Lawaetz Schultz, Helle Krogh Johansen, et al.
The European Respiratory Journal
|
September 5, 2014
Low socioeconomic status is associated with worse lung function in the Danish cystic fibrosis population
David C Taylor-Robinson, Karsten Thielen, Tania Pressler, et al.
Pediatric Pulmonology
|
November 5, 2019
Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years
Marianne Skov, Marie Baekvad-Hansen, David M Hougaard, et al.
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of 3