Primary ciliary dyskinesia and cystic fibrosis: Different diseases require different treatment

Chest

Volumn 145, Issue 4, 2014, Pages 674-676

  Lucas, Jane S ^a   Carroll, Mary ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BODY MASS; BRONCHIECTASIS; CILIARY DYSKINESIA; CYSTIC FIBROSIS; DIFFERENTIAL DIAGNOSIS; EDITORIAL; FORCED EXPIRATORY VOLUME; HUMAN; INNATE IMMUNITY; MICROBIOME; MUCOCILIARY CLEARANCE; NUTRITIONAL STATUS; OBSERVATIONAL STUDY; PANCREAS INSUFFICIENCY; PATIENT CARE; POLYMERASE CHAIN REACTION; PRACTICE GUIDELINE; PREVALENCE; PRIORITY JOURNAL; PYROSEQUENCING; QUANTITATIVE ANALYSIS;

CYSTIC FIBROSIS; EXOCRINE PANCREATIC INSUFFICIENCY; FEMALE; HUMANS; KARTAGENER SYNDROME; MALE;

EID: 84898743181     PISSN: 00123692     EISSN: 19313543     Source Type: Journal    
DOI: 10.1378/chest.13-2590     Document Type: Editorial

References (10)

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