X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (198) 198
humans (185) 185
cystic fibrosis (171) 171
respiratory system (124) 124
female (87) 87
male (87) 87
non-cf bronchiectasis (86) 86
bronchiectasis (76) 76
adult (63) 63
pediatrics (61) 61
child (59) 59
children (56) 56
adolescent (53) 53
pseudomonas-aeruginosa (45) 45
pseudomonas aeruginosa (40) 40
cystic fibrosis - microbiology (36) 36
cystic fibrosis - complications (35) 35
pulmonary/respiratory (34) 34
diagnosis (33) 33
health aspects (33) 33
middle aged (32) 32
antibiotics (31) 31
child, preschool (31) 31
cystic fibrosis bronchiectasis (30) 30
microbiology (29) 29
sputum (29) 29
cystic fibrosis - physiopathology (28) 28
disease (28) 28
young adult (28) 28
care and treatment (27) 27
anti-bacterial agents - therapeutic use (26) 26
lung (26) 26
cystic-fibrosis (25) 25
inflammation (25) 25
cystic fibrosis - diagnosis (24) 24
infection (24) 24
patients (23) 23
analysis (22) 22
bronchiectasis - drug therapy (22) 22
cystic fibrosis - therapy (22) 22
lung-disease (22) 22
cystic fibrosis - genetics (21) 21
immunology (21) 21
infectious diseases (21) 21
obstructive pulmonary-disease (21) 21
sputum - microbiology (21) 21
suppurative lung-disease (21) 21
aged (20) 20
animals (20) 20
cf (20) 20
mutation (20) 20
quality of life (20) 20
anti-bacterial agents - administration & dosage (19) 19
chronic disease (19) 19
infant (19) 19
infections (19) 19
lung diseases (19) 19
medical research (19) 19
research (19) 19
administration, inhalation (18) 18
cf patients (18) 18
clinical trials (18) 18
development and progression (18) 18
exacerbations (18) 18
fibrosis (18) 18
pulmonary and respiratory medicine (18) 18
abridged index medicus (17) 17
bacterial infections (17) 17
cystic fibrosis - metabolism (17) 17
cystic fibrosis transmembrane conductance regulator - genetics (17) 17
epidemiology (17) 17
quality-of-life (17) 17
therapy (17) 17
asthma (16) 16
biochemistry & molecular biology (16) 16
bronchiectasis - etiology (16) 16
bronchiectasis - physiopathology (16) 16
critical care medicine (16) 16
internal medicine (16) 16
lung-function (16) 16
pharmacology & pharmacy (16) 16
pseudomonas-aeruginosa infection (16) 16
risk factors (16) 16
adults (15) 15
allergic bronchopulmonary aspergillosis (15) 15
bacteria (15) 15
cf, cystic fibrosis (15) 15
cystic fibrosis - drug therapy (15) 15
cystic fibrosis - epidemiology (15) 15
cystic-fibrosis bronchiectasis (15) 15
mortality (15) 15
pediatrics, perinatology, and child health (15) 15
randomized controlled-trial (15) 15
disease progression (14) 14
genotype (14) 14
long-term (14) 14
management (14) 14
medicine (14) 14
prevalence (14) 14
primary ciliary dyskinesia (14) 14
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Respiratory Research, ISSN 1465-9921, 07/2010, Volume 11, Issue 1, pp. 94 - 94
Background: Microparticles (MPs) are membrane vesicles released during cell activation and apoptosis. MPs have different biological effects depending on the... 
RESPIRATORY-DISEASES | PRIMARY CILIARY DYSKINESIA | ACTIVATION | RESPIRATORY SYSTEM | AIRWAY INFLAMMATION | LUNG-DISEASE | NEUTROPHILS | MICROVESICLES | CIRCULATING MICROPARTICLES | CF AIRWAY | EXPRESSION | Leukocytes - pathology | Sputum - cytology | Humans | Cystic Fibrosis - pathology | GPI-Linked Proteins | Male | Antigens, CD - analysis | Cystic Fibrosis - immunology | Leukocytes - immunology | Young Adult | CD11a Antigen - analysis | Flow Cytometry | CD11b Antigen - analysis | Adult | Cell-Derived Microparticles - pathology | Female | Granulocytes - pathology | Cell-Derived Microparticles - ultrastructure | Macrophages - immunology | Microscopy, Electron, Transmission | Acute Disease | Macrophages - pathology | Immunophenotyping | Particle Size | Phenotype | Cell-Derived Microparticles - immunology | Kartagener Syndrome - pathology | Cell Adhesion Molecules - analysis | Granulocytes - immunology | Cystic fibrosis | Research | Diagnosis | Biological markers | Risk factors | Political activity | Lung diseases | Analysis | Fibrosis | Hostages | Chemical properties | Political aspects | Apoptosis | Index Medicus | Antigens, CD11a | Cell Adhesion Molecules | Leukocytes | Macrophages | Cell-Derived Microparticles | Antigens, CD11b | Life Sciences | Granulocytes | Pulmonology and respiratory tract | Cystic Fibrosis | Kartagener Syndrome | Human health and pathology | Sputum | Antigens, CD
Journal Article
Pediatric, Allergy, Immunology, and Pulmonology, ISSN 2151-321X, 03/2017, Volume 30, Issue 1, pp. 14 - 17
Chronic infections of primary ciliary dyskinesia (PCD) airways are strongly associated with morbidity and mortality; however, relatively limited data exist... 
Primary ciliary dyskinesia | Pathogen | Bronchoalveolar lavage | Sputum | DIAGNOSIS | MANAGEMENT | sputum | FIBROSIS BRONCHIECTASIS | IMMUNOLOGY | BRONCHOSCOPY | CHILDHOOD | NON-CF BRONCHIECTASIS | CHILDREN | FEATURES | ALLERGY | RESPIRATORY SYSTEM | DISEASE | pathogen | PEDIATRICS | bronchoalveolar lavage | primary ciliary dyskinesia
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0124348 - e0124348
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airways and progressive decline in lung function. To gain... 
BACTERIAL DIVERSITY | MULTIDISCIPLINARY SCIENCES | T-RFLP ANALYSIS | PULMONARY EXACERBATION | INFECTION | SPUTUM SAMPLES | RIBOSOMAL-RNA | FEV1 DECLINE | FRAGMENT-LENGTH-POLYMORPHISM | 16S | INSIGHTS | Sputum - microbiology | Lung - microbiology | Pseudomonas aeruginosa - isolation & purification | Cystic Fibrosis - physiopathology | Humans | Male | Molecular Typing | Candida albicans - genetics | Forced Expiratory Volume | Young Adult | Shewanella - isolation & purification | Microbiota | Streptococcus pneumoniae - isolation & purification | Candida albicans - isolation & purification | Streptococcus pneumoniae - genetics | Adult | Female | Burkholderia - genetics | Cystic Fibrosis - microbiology | Shewanella - genetics | Lung - physiopathology | Burkholderia - isolation & purification | Disease Progression | Polymorphism, Restriction Fragment Length | Pseudomonas aeruginosa - genetics | Adolescent | Multiculturalism | Pneumonia | Microbiota (Symbiotic organisms) | Bacterial pneumonia | Analysis | Cystic fibrosis | Health aspects | Pediatrics | Respiratory function | Identification methods | Communities | Lung | Ribosomal DNA | Statistical methods | Biodiversity | Sustainable development | Respiratory tract | Microorganisms | Pseudomonas aeruginosa | Ecological monitoring | Bioindicators | Burkholderia | Significance | Species | Culture | Pathogens | Bacterial infections | Statistical analysis | Lung diseases | Data processing | Patients | Economic development | Children & youth | Biological diversity | Restriction fragment length polymorphism | Antibiotics | Evolutionary biology | Fibrosis | Sputum | Biomarkers | Polymorphism | Index Medicus
Journal Article
Thorax, ISSN 0040-6376, 12/2014, Volume 69, Issue 12, pp. 1073 - 1079
Journal Article