E. De Wachter

发表

Quantitative bone ultrasound at the distal radius in adults with cystic fibrosis.

O. Louis, S. Van Biervliet, J. De Schepper, 2015, Ultrasound in medicine & biology.

CFTR biomarkers: time for promotion to surrogate end-point

M. Amaral, N. Derichs, M. Proesmans, 2012, European Respiratory Journal.

Nutritional Status of Children Hospitalized for Parapneumonic Effusion

Y. Vandenplas, J. De Schepper, A. Malfroot, 2014, PloS one.

Respiratory Bacterial Culture Sampling in Expectorating and Non-expectorating Patients With Cystic Fibrosis

P. Vaes, D. Piérard, A. Malfroot, 2018, Front. Pediatr..

Eradication of chronic methicillin-resistant Staphylococcus aureus infection in cystic fibrosis patients. An observational prospective cohort study of 11 patients.

D. Piérard, W. Vincken, A. Malfroot, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen

J. Verhaegen, O. Soetens, D. Piérard, 2011, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Malacia, inflammation and bronchoalveolar lavage culture in children with persistent respiratory symptoms

F. De Baets, F. Haerynck, A. Malfroot, 2011, European Respiratory Journal.

Rapidly developing Cushing syndrome in a 4-year-old patient during combined treatment with itraconazole and inhaled budesonide

J. De Schepper, A. Malfroot, I. de Schutter, 2003, European Journal of Pediatrics.

Exhaled nitric oxide in stable adult cystic fibrosis patients, during exacerbation and following CFTR-modifying treatment

S. Verbanck, E. Vanderhelst, E. De Wachter, 2019, European Respiratory Journal.

ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria.

C. Castellani, I. Sermet-Gaudelus, K. De Boeck, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

What can the CF registry tell us about rare CFTR-mutations? A Belgian study

S. Seneca, A. Malfroot, S. Wanyama, 2017, Orphanet Journal of Rare Diseases.

Inhaled budesonide induced Cushing's syndrome in cystic fibrosis patients, due to drug inhibition of cytochrome P450.

J. De Schepper, A. Malfroot, I. de Schutter, 2003, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Everything in excess is opposed to nature, even vitamin D: a case report

W. Staels, J. De Schepper, B. Hauser, 2022, Endocrinology, diabetes & metabolism case reports.

Milk protein and Oil‐Red‐O staining of alveolar macrophages in chronic respiratory disease of infancy

F. De Baets, F. Haerynck, A. Malfroot, 2010, Pediatric pulmonology.

In Vitro Susceptibility of Burkholderia cepacia Complex Isolated from Cystic Fibrosis Patients to Ceftazidime-Avibactam and Ceftolozane-Tazobactam

P. Vandamme, C. Peeters, I. Wybo, 2018, Antimicrobial Agents and Chemotherapy.

A model-based economic evaluation of four newborn screening strategies for cystic fibrosis in Flanders, Belgium

S. Simoens, K. Putman, L. Annemans, 2020, Acta clinica Belgica.

Characteristics of Gastroesophageal Reflux and Potential Risk of Gastric Content Aspiration in Children With Cystic Fibrosis

K. Blondeau, D. Sifrim, R. Orel, 2010, Journal of pediatric gastroenterology and nutrition.

Two CFTR mutations within codon 970 differently impact on the chloride channel functionality

G. Castaldo, A. D. Di Lullo, C. Braggion, 2019, Human mutation.

Pulmonary function patterns and their association with genotype and phenotype in adult cystic fibrosis patients

S. Verbanck, W. Vincken, E. Vanderhelst, 2018, Acta clinica Belgica.

The relationship between gastroesophageal reflux and cough in children with chronic unexplained cough using combined impedance–pH–manometry recordings

L. Dupont, K. Blondeau, D. Sifrim, 2011, Pediatric pulmonology.

Strategies for newborn screening for cystic fibrosis: A systematic review of health economic evaluations.

S. Simoens, K. Putman, L. Annemans, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Long-term use of tube feeding in children with cystic fibrosis: results from two Belgian CF centers

F. De Baets, S. Van Biervliet, S. Van daele, 2020, European Journal of Clinical Nutrition.

Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversity

P. Vandamme, V. van Noort, M. Thimmesch, 2021, PLoS pathogens.

Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients

P. Lebecque, M. Vaneechoutte, F. De Baets, 2010, BMC Microbiology.

Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis.

Y. Vandenplas, J. De Schepper, A. Malfroot, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Acute Pain Perception During Different Sampling Methods for Respiratory Culture in Cystic Fibrosis Patients.

P. Vaes, A. Malfroot, H. Eyns, 2017, Journal of pain and symptom management.

Pulmonary disease in cystic fibrosis: assessment with chest CT at chest radiography dose levels.

D. Coomans, B. Ilsen, J. de Mey, 2014, Radiology.

Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.

N. Derichs, P. Melotti, K. De Boeck, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Comparative bone status assessment by dual energy X-ray absorptiometry, peripheral quantitative computed tomography and quantitative ultrasound in adolescents and young adults with cystic fibrosis.

F. De Baets, S. Goemaere, O. Louis, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Factors associated with clinical progression to severe COVID-19 in people with cystic fibrosis: A global observational study

C. Goss, H. Rodgers, P. Burgel, 2022, Journal of Cystic Fibrosis.

ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals.

S. van Koningsbruggen-Rietschel, E. De Wachter, K. Southern, 2024, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Letter to the editor: Risk of false newborn screening after intra-uterine exposure to ETI.

C. Castellani, A. Munck, N. Simmonds, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programme.

J. Barben, E. De Wachter, NJ Simmonds, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A semi-blinded study comparing 2 methods of measuring nasal potential difference: Subcutaneous needle versus dermal abrasion.

R. Buyl, A. Malfroot, I. de Schutter, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.