Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype

American Journal of Respiratory and Critical Care Medicine

Volumn 191, Issue 3, 2015, Pages 316-324

  Davis, Stephanie D ^a   Ferkol, Thomas W ^b   Rosenfeld, Margaret ^c   Lee, Hye Seung ^d   Dell, Sharon D ^e   Sagel, Scott D ^f   Milla, Carlos ^g   Zariwala, Maimoona A ^h   Pittman, Jessica E ^b   Shapiro, Adam J ⁱ   Carson, Johnny L ^h   Krischer, Jeffrey P ^d   Hazucha, Milan J ^h   Cooper, Matthew L ^a   Knowles, Michael R ^h   Leigh, Margaret W ^h  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^d UNIVERSITY OF SOUTH FLORIDA   (United States)

^e HOSPITAL FOR SICK CHILDREN   (Canada)

^f University of Colorado Denver and Children s Hospital Colorado   (United States)

^g STANFORD UNIVERSITY   (United States)

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

ⁱ MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

Cilia; Kartagener syndrome; Respiratory function tests; Ultrastructure; X ray computed tomography scanners

Indexed keywords

DYNEIN ADENOSINE TRIPHOSPHATASE; NITRIC OXIDE; BIOLOGICAL MARKER; CCDC39 PROTEIN, HUMAN; CCDC40 PROTEIN, HUMAN; CYTOSKELETON PROTEIN; PROTEIN;

AIRWAY OBSTRUCTION; ARTICLE; BODY MASS; BRONCHIECTASIS; CHILD; CHILDHOOD DISEASE; CHRONIC COUGH; CILIARY DYSKINESIA; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CROSS-SECTIONAL STUDY; DISEASE SEVERITY; FEMALE; FORCED EXPIRATORY VOLUME; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HAEMOPHILUS INFLUENZAE; HUMAN; LENGTH OF STAY; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; NEONATAL RESPIRATORY DISTRESS SYNDROME; NOSE OBSTRUCTION; OTITIS; PHENOTYPE; PRIORITY JOURNAL; PROSPECTIVE STUDY; PSEUDOMONAS AERUGINOSA; SPIROMETRY; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS PNEUMONIA; THROAT CULTURE; ULTRASTRUCTURE; ADOLESCENT; ALLELE; BIOPSY; BLOOD; CANADA; CLINICAL TRIAL; COMPARATIVE STUDY; GENETICS; KARTAGENER SYNDROME; MULTICENTER STUDY; MUTATION; PRESCHOOL CHILD; SEVERITY OF ILLNESS INDEX; UNITED STATES;

ADOLESCENT; ALLELES; BIOMARKERS; BIOPSY; BODY MASS INDEX; CANADA; CHILD; CHILD, PRESCHOOL; CYTOSKELETAL PROTEINS; FEMALE; GENOTYPE; HUMANS; KARTAGENER SYNDROME; MALE; MUTATION; PHENOTYPE; PROSPECTIVE STUDIES; PROTEINS; SEVERITY OF ILLNESS INDEX; SPIROMETRY; UNITED STATES;

EID: 84922309553     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/rccm.201409-1672OC     Document Type: Article

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