Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
Volume 191, Issue 3, Pages 316-324
Publisher
American Thoracic Society
Online
2014-12-11
DOI
10.1164/rccm.201409-1672oc
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mutations inRSPH1Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype
- (2014) Michael R. Knowles et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Laterality Defects Other Than Situs Inversus Totalis in Primary Ciliary Dyskinesia
- (2014) Adam J Shapiro et al. CHEST
- Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure
- (2014) Mieke Boon et al. Orphanet Journal of Rare Diseases
- Multicenter analysis of body mass index, lung function, and sputum microbiology in primary ciliary dyskinesia
- (2014) Marco Maglione et al. PEDIATRIC PULMONOLOGY
- Body Composition and Pulmonary Function in Cystic Fibrosis
- (2014) Saba Sheikh et al. Frontiers in Pediatrics
- Longitudinal trends in nutritional status and the relation between lung function and BMI in cystic fibrosis: a population-based cohort study
- (2013) Anne L Stephenson et al. AMERICAN JOURNAL OF CLINICAL NUTRITION
- Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease
- (2013) Michael R. Knowles et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Picking up speed: advances in the genetics of primary ciliary dyskinesia
- (2013) Amjad Horani et al. PEDIATRIC RESEARCH
- Mutations inCCDC39andCCDC40are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms
- (2012) Dinu Antony et al. HUMAN MUTATION
- Longitudinal lung function and structural changes in children with primary ciliary dyskinesia
- (2012) Marie Lémery Magnin et al. PEDIATRIC PULMONOLOGY
- Inner dynein arm defects causing primary ciliary dyskinesia: repeat testing required
- (2011) C. O'Callaghan et al. EUROPEAN RESPIRATORY JOURNAL
- Mutations ofDNAH11in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
- (2011) Michael R Knowles et al. THORAX
- Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis
- (2011) S. C. Ranganathan et al. THORAX
- Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial Endpoints
- (2010) Stephanie D. Davis et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Lung Function in Patients with Primary Ciliary Dyskinesia
- (2010) June K. Marthin et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation
- (2010) Anita Becker-Heck et al. NATURE GENETICS
- CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
- (2010) Anne-Christine Merveille et al. NATURE GENETICS
- Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
- (2009) Margaret W Leigh et al. GENETICS IN MEDICINE
- The dynein regulatory complex is the nexin link and a major regulatory node in cilia and flagella
- (2009) Thomas Heuser et al. JOURNAL OF CELL BIOLOGY
- Structural and Functional Lung Disease in Primary Ciliary Dyskinesia
- (2008) Francesca Santamaria et al. CHEST
- Early lung disease in young children with primary ciliary dyskinesia
- (2008) David E. Brown et al. PEDIATRIC PULMONOLOGY
- Reference Ranges for Spirometry Across All Ages
- (2007) Sanja Stanojevic et al. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
- Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused byDNAH11mutations
- (2007) Georg C. Schwabe et al. HUMAN MUTATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search