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The New England journal of medicine, ISSN 1533-4406, 2017, Volume 377, Issue 21, pp. 2013 - 2023
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2015, Volume 373, Issue 3, pp. 220 - 231
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2018, Volume 379, Issue 17, pp. 1612 - 1620
... in patients harboring one or two Phe508del alleles. 
G551D MUTATION | MEDICINE, GENERAL & INTERNAL | TEZACAFTOR-IVACAFTOR | CFTR | Pyrazoles - therapeutic use | Forced Expiratory Volume - drug effects | Humans | Pyrrolidines - administration & dosage | Chloride Channel Agonists - therapeutic use | Male | Aminophenols - therapeutic use | Chloride Channel Agonists - adverse effects | Aminophenols - adverse effects | Pyrrolidines - pharmacology | Pyrrolidines - therapeutic use | Sweat - chemistry | Young Adult | Quinolones - adverse effects | Chlorides - metabolism | Quinolones - therapeutic use | Adult | Benzodioxoles - adverse effects | Female | Benzodioxoles - therapeutic use | Pyrazoles - pharmacology | Pyridines - therapeutic use | Pyridines - administration & dosage | Double-Blind Method | Genotype | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Chlorides - analysis | Pyrazoles - administration & dosage | Indoles - adverse effects | Cystic Fibrosis - genetics | Adolescent | Alleles | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Indoles - therapeutic use | Pyridines - pharmacology | Mutation | Cystic Fibrosis - drug therapy | Drug Combinations | Cystic fibrosis | Ivacaftor | Dosage and administration | Drug therapy | Statistical analysis | Writers | Epithelial cells | Chloride transport | Recovery of function | Patients | Design | Proteins | Genotype & phenotype | Chloride | Collaboration | Conductance | Cystic fibrosis transmembrane conductance regulator | Protein transport | Sweat | Pharmaceuticals
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2018, Volume 379, Issue 17, pp. 1599 - 1611
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2011, Volume 365, Issue 18, pp. 1663 - 1672
Journal Article
Chest, ISSN 0012-3692, 05/2017, Volume 151, Issue 5, pp. 982 - 992
Objectives We sought to describe the characteristics of adult patients with bronchiectasis enrolled in the US Bronchiectasis Research Registry (BRR... 
registry | airways | nontuberculous mycobacteria | Pseudomonas | bronchiectasis | LUNG-FUNCTION | PULMONARY-FUNCTION | NON-CF BRONCHIECTASIS | RESPIRATORY SYSTEM | CYSTIC FIBROSIS BRONCHIECTASIS | PSEUDOMONAS-AERUGINOSA | INFECTION | CRITICAL CARE MEDICINE | Spirometry | United States - epidemiology | Humans | Middle Aged | Hispanic Americans - statistics & numerical data | Male | Tomography, X-Ray Computed | Gastroesophageal Reflux - epidemiology | Sinusitis - epidemiology | Forced Expiratory Volume | Mycobacterium Infections, Nontuberculous - microbiology | Adult | Biomedical Research | Female | Registries | Insurance, Health | Staphylococcus aureus | Asthma - epidemiology | Nontuberculous Mycobacteria | Ethnic Groups - statistics & numerical data | Immunologic Deficiency Syndromes - epidemiology | Comorbidity | European Continental Ancestry Group - statistics & numerical data | Kartagener Syndrome - epidemiology | Bronchiectasis - microbiology | Mycobacterium Infections, Nontuberculous - epidemiology | Vital Capacity | African Americans - statistics & numerical data | Animals | Staphylococcal Infections - epidemiology | Pseudomonas Infections - epidemiology | Bronchiectasis - epidemiology | Smoking - epidemiology | Otitis - epidemiology | Aged | Rhinitis - epidemiology | Bronchiectasis - physiopathology | Antibiotics | Adults | Dosage and administration | Bronchiectasis | Diagnosis | Research | Health aspects | PEP, positive expiratory pressure | BRR, Bronchiectasis Research Registry | NCFB, non-cystic-fibrosis bronchiectasis | LUL, left upper lobe | CF, cystic fibrosis | AFB, acid-fast bacillus | NTM, nontuberculous mycobacteria | RUL, right upper lobe | GERD, gastroesophageal reflux | DCC, data coordinating center | RML, right middle lobe
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 2013, Volume 131, Issue 4, pp. 1117 - 1129.e5
.... Objective We set out to determine the frequency of TH 17 cells in patients with cystic fibrosis (CF... 
Allergy and Immunology | memory T-cell response | TH22 | Aspergillus species | lung transplant | cystic fibrosis | IL-17 | Pseudomonas species | chronic infectious disease | TH17 | IL-22 | IL-17 RECEPTOR | TGF-BETA | COLONY-STIMULATING FACTOR | MUCOSAL HOST-DEFENSE | IMMUNOLOGY | NEUTROPHIL RECRUITMENT | MATRIX METALLOPROTEINASES | OBSTRUCTIVE PULMONARY-DISEASE | ALLERGY | REGULATORY T-CELLS | KLEBSIELLA-PNEUMONIAE | TH17 CELLS | Lymph Nodes - pathology | Humans | Middle Aged | Antigens, Bacterial - immunology | Aspergillus - chemistry | Cystic Fibrosis - pathology | Interleukin-17 - immunology | Male | Case-Control Studies | Cystic Fibrosis - immunology | Interleukins - genetics | Th17 Cells - drug effects | Antigens, Fungal - pharmacology | Interleukins - immunology | Adult | Female | Lymph Nodes - drug effects | Th17 Cells - pathology | Gene Expression | Lung - pathology | Interleukin-17 - genetics | Antigens, Bacterial - pharmacology | Immunophenotyping | Antigens, Fungal - immunology | Lymph Nodes - immunology | Pseudomonas aeruginosa - chemistry | Lymphocyte Activation - drug effects | Cystic Fibrosis - genetics | Lung - drug effects | Th17 Cells - immunology | Immunologic Memory | Aged | Cell Proliferation - drug effects | Lung - immunology | Studies | Human subjects | Antigens | Transplants & implants | Disease | Lungs | Review boards | Cystic fibrosis | Chronic obstructive pulmonary disease | Fungal infections | Immune system
Journal Article
American journal of respiratory and critical care medicine, ISSN 1535-4970, 2013, Volume 187, Issue 11, pp. 1219 - 1225
Journal Article
Chest, ISSN 0012-3692, 2016, Volume 149, Issue 2, pp. 390 - 400
.... Methods We performed a retrospective analysis using data reported to the Cystic Fibrosis Foundation Patient Registry (CFFPR... 
Pulmonary/Respiratory | registry | Pseudomonas aeruginosa | cystic fibrosis | Staphylococcus aureus | Cystic fibrosis | Registry | UNITED-STATES | NONTUBERCULOUS MYCOBACTERIA | ACQUISITION | ABSCESSUS | RESISTANT STAPHYLOCOCCUS-AUREUS | STENOTROPHOMONAS-MALTOPHILIA | PSEUDOMONAS-AERUGINOSA INFECTION | RESPIRATORY SYSTEM | MRSA | MOLECULAR EPIDEMIOLOGY | PATHOGENS | CRITICAL CARE MEDICINE | United States - epidemiology | Age Distribution | Prevalence | Bacterial Infections - etiology | Humans | Child, Preschool | Infant | Male | Respiratory System - microbiology | Incidence | Young Adult | Adult | Female | Registries | Retrospective Studies | Child | Infant, Newborn | Cystic Fibrosis - microbiology | Cystic Fibrosis - complications | Cystic Fibrosis - epidemiology | Bacteria - isolation & purification | Adolescent | Bacterial Infections - epidemiology | Sex Distribution | Bacterial Infections - mortality | Care and treatment | Research | Microbiology | Epidemiology | IRB, institutional review board | CF, cystic fibrosis | CFTR, cystic fibrosis transmembrane conductance regulator | NTM, nontuberculous mycobacteria | CFFPR, Cystic Fibrosis Foundation Patient Registry | MSSA, methicillin-susceptible Staphylococcus aureus | CFF, Cystic Fibrosis Foundation | CA, community-associated | Pulmonary Vascular Disease | MRSA, methicillin-resistant Staphylococcus aureus
Journal Article