Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007.
about
Pathophysiology of cystic fibrosis and drugs used in associated digestive tract diseasesUnderstanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal studyAssociation between socioeconomic status, sex, and age at death from cystic fibrosis in England and Wales (1959 to 2008): cross sectional studyCystic fibrosis physicians' perspectives on the timing of referral for lung transplant evaluation: a survey of physicians in the United States.Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis.Global impact of bronchiectasis and cystic fibrosis.Inhaled mannitol for the treatment of cystic fibrosis.Managing the underlying cause of cystic fibrosis: a future role for potentiators and correctors.Cell therapy for cystic fibrosis.Putting lung function and physiology into perspective: cystic fibrosis in adults.Does current reporting of lung function by the UK cystic fibrosis registry allow a fair comparison of adult centres?Eosinophilic Otitis Media: the Aftermath of Eosinophil Extracellular Trap Cell Death.Survival Comparison of Patients With Cystic Fibrosis in Canada and the United States: A Population-Based Cohort Study.Lung transplantation for cystic fibrosis: an update.Immunomodulatory Cell Therapy to Target Cystic Fibrosis Inflammation.Consequences of Expiratory Flow Limitation at Rest in Subjects with Cystic Fibrosis.Heterogeneity in Survival in Adult Patients With Cystic Fibrosis With FEV1 < 30% of Predicted in the United States.Lung function comparison between two decades in cystic fibrosis children: A single centre study.Effect of dornase alfa on inflammation and lung function: potential role in the early treatment of cystic fibrosis.Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis.Physiological markers of exercise capacity and lung disease severity in cystic fibrosis.Estimating peak oxygen uptake in adolescents with cystic fibrosis.Cystic Fibrosis: The Dawn of a New Therapeutic Era.Chest computed tomography scores are predictive of survival in patients with cystic fibrosis awaiting lung transplantation.Prognostication in cystic fibrosis: another futile pastime?ICU outcomes in cystic fibrosis following invasive ventilationAllergic Bronchopulmonary Aspergillosis-A Luminal Hypereosinophilic Disease With Extracellular Trap Cell Death
P2860
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P2860
Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
name
Improved survival at low lung ...... ohort study from 1990 to 2007.
@ast
Improved survival at low lung ...... ohort study from 1990 to 2007.
@en
Improved survival at low lung ...... ohort study from 1990 to 2007.
@nl
type
label
Improved survival at low lung ...... ohort study from 1990 to 2007.
@ast
Improved survival at low lung ...... ohort study from 1990 to 2007.
@en
Improved survival at low lung ...... ohort study from 1990 to 2007.
@nl
prefLabel
Improved survival at low lung ...... ohort study from 1990 to 2007.
@ast
Improved survival at low lung ...... ohort study from 1990 to 2007.
@en
Improved survival at low lung ...... ohort study from 1990 to 2007.
@nl
P2093
P2860
P356
P1433
P1476
Improved survival at low lung ...... ohort study from 1990 to 2007.
@en
P2093
M E Hodson
N J Simmonds
P Cullinan
P M George
P2860
P356
10.1136/BMJ.D1008
P407
P577
2011-02-28T00:00:00Z