"cystic fibrosis" trang 3 - tải miễn phí từ tailieuXANH
Airway, but not serum or urinary, levels of YKL-40 reflect inflammation in early cystic fibrosis lung disease

Airway, but not serum or urinary, levels of YKL-40 reflect inflammation in early cystic fibrosis lung disease
6    35    1
Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene

Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene
7    36    1
Determinants of exercise capacity in cystic fibrosis patients with mild-to-moderate lung disease

Determinants of exercise capacity in cystic fibrosis patients with mild-to-moderate lung disease
8    47    1
Dynamics of soluble and cellular inflammatory markers in nasal lavage obtained from Cystic Fibrosis patients during intravenous antibiotic treatment

Dynamics of soluble and cellular inflammatory markers in nasal lavage obtained from Cystic Fibrosis patients during intravenous antibiotic treatment
11    31    1
Role of C-reactive protein as a biomarker for prediction of the severity of pulmonary exacerbations in patients with cystic fibrosis

Role of C-reactive protein as a biomarker for prediction of the severity of pulmonary exacerbations in patients with cystic fibrosis
8    29    1
Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: A case-control study

Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: A case-control study
10    51    1
Self-reported exercise and longitudinal outcomes in cystic fibrosis: A retrospective cohort study

Self-reported exercise and longitudinal outcomes in cystic fibrosis: A retrospective cohort study
8    209    1
Subcutaneous implant with etonogestrel (Implanon®) for catamenial exacerbations in a patient with cystic fibrosis: A case report

Subcutaneous implant with etonogestrel (Implanon®) for catamenial exacerbations in a patient with cystic fibrosis: A case report
4    33    1
Symptoms of depression impact the course of lung function in adolescents and adults with cystic fibrosis

Symptoms of depression impact the course of lung function in adolescents and adults with cystic fibrosis
6    31    1
Demographic, clinical, and laboratory parameters of cystic fibrosis during the last two decades: A comparative analysis

Demographic, clinical, and laboratory parameters of cystic fibrosis during the last two decades: A comparative analysis
12    33    1
Data driven decision making to characterize clinical personas of parents of children with cystic fibrosis: A mixed methods study

Data driven decision making to characterize clinical personas of parents of children with cystic fibrosis: A mixed methods study
14    53    1
Worsening pulmonary outcomes during sex reassignment therapy in a transgender female with cystic fibrosis (CF) and asthma/ allergic bronchopulmonary aspergillosis: A case report

Worsening pulmonary outcomes during sex reassignment therapy in a transgender female with cystic fibrosis (CF) and asthma/ allergic bronchopulmonary aspergillosis: A case report
4    40    1
New strategies of physical activity assessment in cystic fibrosis: A pilot study

New strategies of physical activity assessment in cystic fibrosis: A pilot study
9    49    1
Rapidly progressive metastatic cholangiocarcinoma in a postpartum patient with cystic fibrosis: A case report

Rapidly progressive metastatic cholangiocarcinoma in a postpartum patient with cystic fibrosis: A case report
5    58    1
An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa

An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa
8    51    1
Size-adjusted muscle power and muscle metabolism in patients with cystic fibrosis are equal to healthy controls – a case control study

Size-adjusted muscle power and muscle metabolism in patients with cystic fibrosis are equal to healthy controls – a case control study
11    37    1
Current infection control practices used in Australian and New Zealand cystic fibrosis centers

Current infection control practices used in Australian and New Zealand cystic fibrosis centers
8    41    1
Microbial contamination of home nebulizers in children with cystic fibrosis and clinical implication on the number of pulmonary exacerbations

Microbial contamination of home nebulizers in children with cystic fibrosis and clinical implication on the number of pulmonary exacerbations
8    35    1
Lung transplant referral practice patterns: A survey of cystic fibrosis physicians and general pulmonologists

Lung transplant referral practice patterns: A survey of cystic fibrosis physicians and general pulmonologists
9    47    1
Unilateral temporary diaphragmatic paralysis secondary to bronchial artery embolization in a girl with cystic fibrosis and massive hemoptysis: A case report

Unilateral temporary diaphragmatic paralysis secondary to bronchial artery embolization in a girl with cystic fibrosis and massive hemoptysis: A case report
3    84    1
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