Nasal mucociliary transport and ciliary ultrastructure in cystic fibrosis. A comparative study with healthy volunteers

International Journal of Pediatric Otorhinolaryngology

Volumn 40, Issue 1, 1997, Pages 27-34

  Armengot, M ^a,d   Escribano, A ^b   Carda, C ^c   Sanchez C ^b   Romero, C ^b   Basterra, J ^a  

^a HOSPITAL GENERAL UNIVERSITARIO DE VALENCIA   (Spain)

^b HOSPITAL CLÍNICO UNIVERSITARIO   (Spain)

^c UNIVERSITY OF VALENCIA   (Spain)

^d NONE   (Spain)

Author keywords

Cystic fibrosis; Mucociliary function; Mucoviscidosis

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL ULTRASTRUCTURE; CHILD; CHROMOSOME 7; CHRONIC DISEASE; CILIARY MOTILITY; CLINICAL ARTICLE; COMPARATIVE STUDY; CYSTIC FIBROSIS; FEMALE; HUMAN; LUNG INJURY; MALE; MUCOCILIARY TRANSPORT; NOSE MUCOSA; PRIORITY JOURNAL; RESPIRATORY EPITHELIUM; RESPIRATORY TRACT INFECTION;

ADOLESCENT; ADULT; BIOLOGICAL TRANSPORT; CHILD; CHILD, PRESCHOOL; CILIA; CYSTIC FIBROSIS; DISEASE SUSCEPTIBILITY; FEMALE; HUMANS; MALE; MUCOCILIARY CLEARANCE; MUCUS; NASAL MUCOSA; PSEUDOMONAS INFECTIONS; REFERENCE VALUES; RESPIRATORY TRACT INFECTIONS;

EID: 0030914028     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(97)01490-0     Document Type: Article

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