scholarly article | Q13442814 |
P2093 | author name string | P M George | |
M E Hodson | |||
P Cullinan | |||
D Bilton | |||
N J Simmonds | |||
W Banya | |||
N Pareek | |||
P2860 | cites work | Dornase alfa for cystic fibrosis | Q24236803 |
Nebulised hypertonic saline for cystic fibrosis | Q24241042 | ||
Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease | Q29618681 | ||
Timing of referral for lung transplantation for cystic fibrosis: overemphasis on FEV1 may adversely affect overall survival | Q33543150 | ||
Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study | Q33801253 | ||
Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group | Q34290556 | ||
Gender gap in cystic fibrosis mortality | Q34425312 | ||
Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project | Q35535262 | ||
Cystic fibrosis: current survival and population estimates to the year 2000. | Q36253480 | ||
Medium term treatment of stable stage cystic fibrosis with recombinant human DNase I. | Q36548175 | ||
Survival effect of lung transplantation among patients with cystic fibrosis | Q36848757 | ||
Determinants of mortality from cystic fibrosis in Canada, 1970-1989. | Q43698922 | ||
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial | Q44602962 | ||
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis | Q46900190 | ||
A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities | Q46922742 | ||
Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis | Q47739161 | ||
Risk of death in cystic fibrosis patients with severely compromised lung function. | Q50887135 | ||
An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years. | Q51120992 | ||
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. | Q51711090 | ||
Noninvasive ventilation in cystic fibrosis patients with acute or chronic respiratory failure. | Q51726178 | ||
International guidelines for the selection of lung transplant candidates: 2006 update--a consensus report from the Pulmonary Scientific Council of the International Society for Heart and Lung Transplantation. | Q53253288 | ||
Efficacy of aerosolized tobramycin in patients with cystic fibrosis. | Q54237890 | ||
Effect of Treatment with Dornase Alpha on Airway Inflammation in Patients with Cystic Fibrosis | Q61791581 | ||
Prediction of Mortality in Patients with Cystic Fibrosis | Q67469870 | ||
Diabetes mellitus associated with cystic fibrosis | Q68276767 | ||
Comparison of effectiveness of pancreatic enzyme preparations in cystic fibrosis | Q70533113 | ||
Standardised lung function testing | Q70587808 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | cystic fibrosis | Q178194 |
P304 | page(s) | d1008 | |
P577 | publication date | 2011-02-28 | |
P1433 | published in | The BMJ | Q546003 |
P1476 | title | Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. | |
P478 | volume | 342 |
Q58572838 | Allergic Bronchopulmonary Aspergillosis-A Luminal Hypereosinophilic Disease With Extracellular Trap Cell Death |
Q47103711 | Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis |
Q35178544 | Association between socioeconomic status, sex, and age at death from cystic fibrosis in England and Wales (1959 to 2008): cross sectional study |
Q64111377 | Cardiopulmonary Exercise Testing: Another Tool in the Prognostication Tool Kit for Cystic Fibrosis |
Q38124849 | Cell therapy for cystic fibrosis |
Q53171875 | Chest computed tomography scores are predictive of survival in patients with cystic fibrosis awaiting lung transplantation. |
Q39740014 | Consequences of Expiratory Flow Limitation at Rest in Subjects with Cystic Fibrosis. |
Q51424428 | Cystic Fibrosis: The Dawn of a New Therapeutic Era. |
Q89219005 | Cystic fibrosis |
Q36254493 | Cystic fibrosis physicians' perspectives on the timing of referral for lung transplant evaluation: a survey of physicians in the United States. |
Q38809559 | Does current reporting of lung function by the UK cystic fibrosis registry allow a fair comparison of adult centres? |
Q60922612 | Dynamic Prediction of Survival in Cystic Fibrosis: A Landmarking Analysis Using UK Patient Registry Data |
Q42728646 | Effect of dornase alfa on inflammation and lung function: potential role in the early treatment of cystic fibrosis |
Q38813293 | Eosinophilic Otitis Media: the Aftermath of Eosinophil Extracellular Trap Cell Death. |
Q51181329 | Estimating peak oxygen uptake in adolescents with cystic fibrosis. |
Q37631978 | Global impact of bronchiectasis and cystic fibrosis |
Q40361294 | Heterogeneity in Survival in Adult Patients With Cystic Fibrosis With FEV1 < 30% of Predicted in the United States |
Q57651819 | ICU outcomes in cystic fibrosis following invasive ventilation |
Q39434813 | Immunomodulatory Cell Therapy to Target Cystic Fibrosis Inflammation |
Q37979246 | Inhaled mannitol for the treatment of cystic fibrosis |
Q40973759 | Lung function comparison between two decades in cystic fibrosis children: A single centre study |
Q92705518 | Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines |
Q39008114 | Lung transplantation for cystic fibrosis: an update |
Q38178773 | Management of comorbidities in older patients with cystic fibrosis. |
Q38113749 | Managing the underlying cause of cystic fibrosis: a future role for potentiators and correctors |
Q38139191 | Nontuberculous mycobacteria: the changing epidemiology and treatment challenges in cystic fibrosis. |
Q26825799 | Pathophysiology of cystic fibrosis and drugs used in associated digestive tract diseases |
Q47381971 | Physiological markers of exercise capacity and lung disease severity in cystic fibrosis |
Q54652020 | Prognostication in cystic fibrosis: another futile pastime? |
Q38248996 | Putting lung function and physiology into perspective: cystic fibrosis in adults |
Q59510282 | Referral to lung transplantation- too little, too late |
Q38910874 | Survival Comparison of Patients With Cystic Fibrosis in Canada and the United States: A Population-Based Cohort Study |
Q90387464 | The future of cystic fibrosis care: a global perspective |
Q28388812 | Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study |
Q36300937 | Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis |
Q89353222 | [Epidemiological trends of cystic fibrosis in France: 10-year perspective] |
Search more.