Diagnosis of primary ciliary dyskinesia: Searching for a gold standard

European Respiratory Journal

Volumn 44, Issue 6, 2014, Pages 1418-1422

  Lucas, Jane S ^a,b   Leigh, Margaret W ^c  

^a UNIVERSITY HOSPITAL SOUTHAMPTON NHS FOUNDATION TRUST   (United Kingdom)

^b UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CILIARY DYSKINESIA; CILIARY MOTILITY; CLINICAL PROTOCOL; DNAI1 GENE; EUROPEAN; EVIDENCE BASED PRACTICE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; GOLD STANDARD; HIGH SPEED VIDEO MICROSCOPY ANALYSIS; HUMAN; MEDICAL SOCIETY; NATIONAL HEALTH SERVICE; NITRIC OXIDE ANALYZER; PRACTICE GUIDELINE; REVIEW; TRANSMISSION ELECTRON MICROSCOPY; UNITED KINGDOM; VIDEO MICROSCOPY; EUKARYOTIC FLAGELLUM; KARTAGENER SYNDROME; PATHOPHYSIOLOGY; PHYSIOLOGY;

CILIA; HUMANS; KARTAGENER SYNDROME;

EID: 84916203838     PISSN: 09031936     EISSN: 13993003     Source Type: Journal    
DOI: 10.1183/09031936.00175614     Document Type: Review

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