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The New England journal of medicine, ISSN 1533-4406, 2017, Volume 377, Issue 21, pp. 2024 - 2035
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2017, Volume 377, Issue 21, pp. 2013 - 2023
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
Background Monitoring potential changes in the epidemiology of cystic fibrosis (CF) pathogens furthers our understanding of the potential impact of... 
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
Digestive diseases and sciences, ISSN 1573-2568, 2015, Volume 61, Issue 1, pp. 198 - 207
The cystic fibrosis (CF) transmembrane conductance regulator (CFTR) gating mutation G551D prevents sufficient ion transport due to reduced channel-open... 
Growth | FECAL ELASTASE-1 | Kalydeco | CFTR POTENTIATOR | Weight gain | CHILDREN | TRANSMEMBRANE CONDUCTANCE REGULATOR | Bicarbonate | FAT MALABSORPTION | ENERGY-EXPENDITURE | THERAPY | Potentiator | DISEASE | QUALITY-OF-LIFE | Cystic fibrosis transmembrane conductance regulator | BICARBONATE SECRETION | Biochemistry, general | Medicine & Public Health | Hepatology | Gastroenterology | Oncology | Transplant Surgery | GASTROENTEROLOGY & HEPATOLOGY | Cystic Fibrosis - physiopathology | Humans | Male | Young Adult | Time Factors | Adult | Female | Surveys and Questionnaires | Weight Gain - drug effects | Child | Genetic Predisposition to Disease | Double-Blind Method | Drug Administration Schedule | Administration, Oral | Cystic Fibrosis - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - agonists | Treatment Outcome | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Membrane Transport Modulators - administration & dosage | Phenotype | Quinolones - administration & dosage | Cystic Fibrosis - genetics | Nutritional Status - drug effects | Adolescent | Cystic Fibrosis - diagnosis | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Mutation | Aminophenols - administration & dosage | Cystic Fibrosis - drug therapy | Cystic fibrosis | Care and treatment | Genetic aspects | Carbonates | Body image | Analysis
Journal Article
Thorax, ISSN 0040-6376, 01/2012, Volume 67, Issue 1, pp. 12 - 18
Journal Article