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The roles and experiences of adolescents with cystic fibrosis and their parents during transition : a qualitative interview study
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- Journal Article
- A1
- open access
The role and the composition of a liaison team to facilitate the transition of adolescents and young adults : an umbrella review
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- Journal Article
- A1
- open access
Glycemic indices at night measured by CGM are predictive for a lower pulmonary function in adults but not in children with cystic fibrosis
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- Journal Article
- A1
- open access
Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic
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- Journal Article
- A1
- open access
Urinary sodium/creatinine ratio is a predictor for fractional sodium excretion and related to age in patients with cystic fibrosis
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Long-term use of tube feeding in children with cystic fibrosis : results from two Belgian CF centers
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Sodiumstatus in patients with cystic fibrosis : how to monitor based on urine sample?
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SeroCovid19 : prospective seroprevalence monitoring reveals substantially reduced SARS-CoV-2 infection rate among tertiary pediatric patients
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Sodium status and replacement in children and adults living with cystic fibrosis : a narrative review
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The nutritional status in CF : being certain about the uncertainties
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Long-term experience with tube feeding in children with cystic fibrosis in two Belgian CF Centers : preliminary results
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Body composition measured by BIA of tube-fed cystic fibrosis patients compared to age-sex matched controls
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The effect of enteral tube feeding in cystic fibrosis : a registry based study
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Risk factors and impact of allergic bronchopulmonary aspergillosis in Pseudomonas aeruginosa-negative CF patients
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Establishing the diagnosis of chronic colonization with Pseudomonas aeruginosa of cystic fibrosis patients : comparison of the European consensus criteria with genotyping of P. aeruginosa isolates
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When one rare disease hides another : Kartagener syndrome masking FMF
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Development and validation of an LC tandem MS assay for the quantification of β-lactam antibiotics in the sputum of cystic fibrosis patients
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- Journal Article
- A1
- open access
A CARD9 founder mutation disrupts NF-κB signaling by inhibiting BCL10 and MALT1 recruitment and signalosome formation
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Single centre long-term experience with tube feeding in children with cystic fibrosis
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Evaluation of HbA1c and OGTT-results after a first abnormal OGTT
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Impact of tube feeding (TF) on pulmonary function in children and adults with cystic fibrosis
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Characteristics at baseline of tube-fed cystic fibrosis (CF) patients with matched controls : a registry study
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The impact of tube feeding in children and adults with cystic fibrosis
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- Journal Article
- A1
- open access
Effects of propidium monoazide (PMA) treatment on mycobiome and bacteriome analysis of cystic fibrosis airways during exacerbation
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Exercise performance and quality of life in children with cystic fibrosis and mildly impaired lung function : relation with antibiotic treatments and hospitalization
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Gastro-intestinal manifestations in cystic fibrosis patients
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When two rare diseases coincide : Kartagener Syndrome and Familial Mediterranean Fever
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- Conference Paper
- C3
- open access
Communication in healthcare: a narrative review of the literature and practical recommendations
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- Journal Article
- A1
- open access
Epidemic Achromobacter xylosoxidans strain among Belgian cystic fibrosis patients and review of literature
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Chronic and invasive fungal infections in a family with CARD9 deficiency (vol 36, pg 204, 2016)
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Chronic and invasive fungal infections in a family with CARD9 deficiency
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ABPAs in Pseudomonas aeruginosa colonized CF patients
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Colistin and neurotoxicity : recommendations for optimal use in cystic fibrosis patients
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Achromobacter xylosoxidans/ruhlandii colonized CF patients have more hospitalisations and IV antibiotic days
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Validity of the oxygen uptake efficiency slope (OUES) as a parameter of maximal and submaximal exercise testing in children with mild CF
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Impact van communicatie tussen zorgverstrekkers op de kwaliteit van patiëntenzorg
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Pseudomonas aeruginosa genotyping: predicting transition to chronic colonization in cystic fibrosis patients
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- Journal Article
- A1
- open access
Communication in healthcare : a narrative review of the literature and practical recommendations
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A single clone of Achromobacter xylosoxidans colonizes Belgian cystic fibrosis patients from different centres
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Quantitative bone ultrasound at the distal radius in adults with cystic fibrosis
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Psychiatrische aandoeningen bij mucoviscidose: een overzicht
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Aspergillus nodi in cystic fibrosis (CF) patients: a rare entity: report of two pediatric cases
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Achromobacter xylosoxidans induced bronchiolitis obliterans in cystic fibrosis
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De impact van communicatie tussen zorgverstrekkers op de kwaliteit van patiëntenzorg
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ABPA syndrome (ABPAs) in CF : FEV1 decline, infectious exacerbations and BMI before and after the year of diagnosis (index year), a case control study
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Genotyping of Achromobacter xylosoxidans in a cystic fibrosis (CF) centre
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- Journal Article
- A1
- open access
Primary ciliary dyskinesia : critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure
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- Journal Article
- A1
- open access
Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis
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Eradication therapy for Pseudomonas aeruginosa colonization episodes in cystic fibrosis patients not chronically colonized by P. aeruginosa
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- Journal Article
- A1
- open access
Is the improvement of CF patients, hospitalized for pulmonary exacerbation, correlated to a decrease in bacterial load?
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Genetic variations in toll-like receptor pathway and lung function decline in Cystic Fibrosis patients
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Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms
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Genetic variations in toll-like receptor pathway and lung function decline in cystic fibrosis patients
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Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients
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Neonatal pulmonary interstitial glycogenosis in a patient with Hunter syndrome
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PCR and the detection of Pseudomonas aeruginosa in respiratory samples of CF patients: a literature review
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Genotype based evaluation of Pseudomonas aeruginosa eradication treatment success in cystic fibrosis patients
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Milk protein and Oil-Red-O staining of alveolar macrophages in chronic respiratory disease of infancy
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- Journal Article
- A1
- open access
Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients
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Een pediatrische patiënt met het syndroom van Lemierre
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Genotype based evaluation of eradication treatment success for new Pseudomonas aeruginosa infections in cystic fibrosis patients
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- Journal Article
- A1
- open access
Comparison of the sensitivity of culture, PCR and quantitative real-time PCR for the detection of Pseudomonas aeruginosa in sputum of cystic fibrosis patients
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Severe corticosteroid-dependent asthma in association with eczema and type 1 diabetes mellitus as an early manifestation of the IPEX syndrome: a case report
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Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients
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Achromobacter xylosoxidans in cystic fibrosis: Prevalence and clinical relevance
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Single nucleotide polymorphisms in genes of the innate immunity in cystic fibrosis patients: Correlation with lung function and pseudomonas aeruginosa colonisation
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- PhD Thesis
- open access
Epidemiology of Pseudomomas aeruginosa and Achromobacter xylosoxidans in Belgian cystic fibrosis patients, relying on molecular typing techniques
(2006) -
Perinatale aanpak bij congenitale luchtwegmalformaties
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Evidence for autosomal dominant inheritance in prenatally diagnosed CHAOS
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Survey of Pseudomonas aeruginosa genotypes in colonised cystic fibrosis patients
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Exercise-induced respiratory symptoms are poor predictors of bronchoconstriction
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Shared genotypes of Achromobacter xylosoxidans strains isolated from patients at a cystic fibrosis rehabilitation center
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Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centre
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Evidence for autosomal dominant inheritance in prenatally diagnosed CHAOS
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Asphyxiating tracheal bronchogenic cyst
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Een geconjugeerd pneumococcen vaccin voor kinderen.
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Diagnose en beleid van pseudo-kroep en epiglottitis
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Inhaled steroids compared with disodium cromoglycate in preschool children with episodic viral wheeze.
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Astma op kleuterleeftijd: astma?
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Cytogenetic analysis of a mesenchymal hamartoma of the liver