Found: 60
Select item for more details and to access through your institution.
Decoding negative genetic panels in primary ciliary dyskinesia.
- Published in:
- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 784, doi. 10.1002/ppul.26790
- By:
- Publication type:
- Article
Hypoglycemia in children and young adults with cystic fibrosis during oral glucose tolerance testing vs. continuous glucose monitoring.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 9, p. 2495, doi. 10.1002/ppul.26533
- By:
- Publication type:
- Article
Clinical characteristics of people with cystic fibrosis and frequent fungal infection.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 1, p. 152, doi. 10.1002/ppul.25741
- By:
- Publication type:
- Article
Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 1, p. 130, doi. 10.1002/ppul.24528
- By:
- Publication type:
- Article
Population Genomics and Inference of Mycobacterium avium Complex Clusters in Cystic Fibrosis Care Centers, United States.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Predicting return of lung function after a pulmonary exacerbation using the cystic fibrosis respiratory symptom diary-chronic respiratory infection symptom scale.
- Published in:
- BMC Pulmonary Medicine, 2024, p. 1, doi. 10.1186/s12890-024-03148-w
- By:
- Publication type:
- Article
Predicting return of lung function after a pulmonary exacerbation using the cystic fibrosis respiratory symptom diary-chronic respiratory infection symptom scale.
- Published in:
- BMC Pulmonary Medicine, 2024, p. 1, doi. 10.1186/s12890-024-03148-w
- By:
- Publication type:
- Article
Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 4, p. 539, doi. 10.1513/AnnalsATS.202206-524OC
- By:
- Publication type:
- Article
Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 3, p. 397, doi. 10.1513/AnnalsATS.202206-487OC
- By:
- Publication type:
- Article
Airway Inflammation in Children with Primary Ciliary Dyskinesia.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 1, p. 67, doi. 10.1513/AnnalsATS.202204-314OC
- By:
- Publication type:
- Article
Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia.
- Published in:
- Annals of the American Thoracic Society, 2022, v. 19, n. 11, p. 1865, doi. 10.1513/AnnalsATS.202202-116OC
- By:
- Publication type:
- Article
Population Genomics of from U.S. Cystic Fibrosis Care Centers.
- Published in:
- Annals of the American Thoracic Society, 2021, v. 18, n. 12, p. 1960, doi. 10.1513/AnnalsATS.202009-1214OC
- By:
- Publication type:
- Article
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection.
- Published in:
- BMC Microbiology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12866-023-03073-8
- By:
- Publication type:
- Article
Clinical outcomes in U.S. infants with cystic fibrosis from 2001 to 2012.
- Published in:
- Pediatric Pulmonology, 2018, v. 53, n. 11, p. 1492, doi. 10.1002/ppul.24165
- By:
- Publication type:
- Article
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.
- Published in:
- Pediatric Pulmonology, 2016, v. 51, n. 2, p. 115, doi. 10.1002/ppul.23304
- By:
- Publication type:
- Article
Sputum induction improves detection of pathogens in children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 7, p. 638, doi. 10.1002/ppul.23150
- By:
- Publication type:
- Article
Novel outcome measures for clinical trials in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 3, p. 302, doi. 10.1002/ppul.23146
- By:
- Publication type:
- Article
Urinary desmosine: A biomarker of structural lung injury during CF pulmonary exacerbation.
- Published in:
- Pediatric Pulmonology, 2012, v. 47, n. 9, p. 856, doi. 10.1002/ppul.22525
- By:
- Publication type:
- Article
Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience.
- Published in:
- Pediatric Pulmonology, 2011, v. 46, n. 5, p. 483, doi. 10.1002/ppul.21402
- By:
- Publication type:
- Article
Pulmonary exacerbations in cystic fibrosis with negative bacterial cultures.
- Published in:
- Pediatric Pulmonology, 2010, v. 45, n. 6, p. 569, doi. 10.1002/ppul.21221
- By:
- Publication type:
- Article
Relationship between antimicrobial proteins and airway inflammation and infection in cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2009, v. 44, n. 4, p. 402, doi. 10.1002/ppul.21028
- By:
- Publication type:
- Article
Effects of sildenafil on pulmonary hypertension and exercise tolerance in severe cystic fibrosis‐related lung diseaseConflict of interest statement: G.S.M., S.D.S., A.L.T., and S.H.A. have no conflicts of interest to disclose.
- Published in:
- Pediatric Pulmonology, 2006, v. 41, n. 4, p. 383, doi. 10.1002/ppul.20393
- By:
- Publication type:
- Article
Response to Letter by Ren.
- Published in:
- Pediatric Pulmonology, 2005, v. 40, n. 3, p. 276, doi. 10.1002/ppul.20269
- By:
- Publication type:
- Article
Induced sputum matrix metalloproteinase-9 correlates with lung function and airway inflammation in children with cystic fibrosis.
- Published in:
- Pediatric Pulmonology, 2005, v. 39, n. 3, p. 224, doi. 10.1002/ppul.20165
- By:
- Publication type:
- Article
Inflammation and Airway Microbiota during Cystic Fibrosis Pulmonary Exacerbations.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062917
- By:
- Publication type:
- Article
<i>Mycobacterium abscessus</i> Induces a Limited Pattern of Neutrophil Activation That Promotes Pathogen Survival.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057402
- By:
- Publication type:
- Article
Reliability of Quantitative Real-Time PCR for Bacterial Detection in Cystic Fibrosis Airway Specimens.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0015101
- By:
- Publication type:
- Article
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Clinical Effectiveness of Elexacaftor/Tezacftor/Ivacaftor in People with Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 205, n. 5, p. 1, doi. 10.1164/rccm.202108-1986oc
- By:
- Publication type:
- Article
Females with Cystic Fibrosis Demonstrate a Differential Response Profile to Ivacaftor Compared with Males.
- Published in:
- 2020
- By:
- Publication type:
- Letter
CC16: A Biomarker of Pollutant Exposure and Future Lung Disease?
- Published in:
- 2019
- By:
- Publication type:
- journal article
Shifting Landscape of Airway Infection in Early Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2019, v. 200, n. 5, p. 528, doi. 10.1164/rccm.201903-0529ED
- By:
- Publication type:
- Article
Shifting Landscape of Airway Infection in Early Cystic Fibrosis.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Effects of an Antioxidant-enriched Multivitamin in Cystic Fibrosis. A Randomized, Controlled, Multicenter Clinical Trial.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Changes in Lung Clearance Index in Preschool-aged Patients with Cystic Fibrosis Treated with Ivacaftor (GOAL): A Clinical Trial.
- Published in:
- 2018
- By:
- Publication type:
- Letter
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Primary Ciliary Dyskinesia in Children: A Review for Pediatricians, Allergists, and Pediatric Pulmonologists.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Primary Ciliary Dyskinesia in Children: A Review for Pediatricians, Allergists, and Pediatric Pulmonologists.
- Published in:
- Pediatric Allergy, Immunology & Pulmonology, 2011, v. 24, n. 4, p. 191, doi. 10.1089/ped.2011.0099
- By:
- Publication type:
- Article
Students Teaching AIDS to Students (STATS).
- Published in:
- Public Health Reports, 1995, v. 110, n. 2, p. 209
- By:
- Publication type:
- Article
Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2015, v. 191, n. 3, p. 316, doi. 10.1164/rccm.201409-1672OC
- By:
- Publication type:
- Article
Clinical Mechanism of the CFTR Potentiator Ivacaftor in G551D-Mediated Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 2, p. E1, doi. 10.1164/rccm.201404-0703oc
- By:
- Publication type:
- Article
Clinical Mechanism of the Cystic Fibrosis Transmembrane Conductance Regulator Potentiator Ivacaftor in G551D-mediated Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 2, p. 175, doi. 10.1164/rccm.201404-0703OC
- By:
- Publication type:
- Article
Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 189, n. 6, p. 707, doi. 10.1164/rccm.201311-2047OC
- By:
- Publication type:
- Article
Sputum Biomarkers of Inflammation and Lung Function Decline in Children with Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2012, v. 186, n. 9, p. 857, doi. 10.1164/rccm.201203-0507OC
- By:
- Publication type:
- Article
Circulating RNA transcripts identify therapeutic response in cystic fibrosis lung disease.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Association between Pulmonary Function and Sputum Biomarkers in Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2007, v. 175, n. 8, p. 822, doi. 10.1164/rccm.200609-1354oc
- By:
- Publication type:
- Article