about
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile ciliaMCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile ciliaPrimary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure.Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti-Salmonella typhi Vi IgG Describe a Normal Polysaccharide ResponseThe international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results.Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects.Pulmonary alveolar microlithiasis: a case report and review of the literature.Primary ciliary dyskinesia and humoral immunodeficiency--is there a missing link?Morphometric Analysis of Explant Lungs in Cystic Fibrosis.Lung structure-function correlation in patients with primary ciliary dyskinesia.Neutrophils from Patients with Primary Ciliary Dyskinesia Display Reduced Chemotaxis to CXCR2 Ligands.Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis.Primary ciliary dyskinesia and humoral immunodeficiency - what is the missing link?Mutations in CCNO and MCIDAS lead to a mucociliary clearance disorder due to reduced generation of multiple motile cilia.Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary Dyskinesia.When One Rare Disease Hides Another: Kartagener Syndrome Masking FMF.Nutritional status, nutrient intake and use of enzyme supplements in paediatric patients with Cystic Fibrosis; a European multicentre study with reference to current guidelines.The Influence of Nebulized Drugs on Nasal Ciliary Activity.Improved repeatability of nasal potential difference with a larger surface catheter.Differential Antiviral Activities of RSV Inhibitors in Human Airway EpitheliumDiagnostic accuracy of nitric oxide measurements to detect primary ciliary dyskinesiaIs the sensitivity of primary ciliary dyskinesia detection by ciliary function analysis 100%?: Table 1–Hemoptysis after orthopedic surgery in an adolescent boyIsolation of Enterobacteriaceae in airway samples is associated with worse outcome in preschool children with cystic fibrosisAssessing gastro-intestinal related quality of life in cystic fibrosis: Validation of PedsQL GI in children and their parentsChest CT scoring for evaluation of lung sequelae in congenital diaphragmatic hernia survivorsThe long-term outcome of an isolated vascular ring - A single-center experience
P50
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P50
description
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հետազոտող
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Mieke Boon
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Mieke Boon
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Mieke Boon
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Mieke Boon
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P1741
P1556
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P1741
P21
P31
P496
0000-0001-8138-5405