Marianne Nuijsink
The Hague, Netherlands
Last Updated: 09/26/2026
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Found 17 publications
Remote monitoring and teleconsultations can reduce greenhouse gas emissions while maintaining quality of care in cystic fibrosis.
Journal: Frontiers in digital health
Published: July 24, 2024
Introduction of Ivacaftor/Lumacaftor in Children With Cystic Fibrosis Homozygous for F508del in the Netherlands: A Nationwide Real-Life Study.
Journal: Pediatric pulmonology
Published: June 03, 2024
Accuracy, Reproducibility, and Responsiveness to Treatment of Home Spirometry in Cystic Fibrosis: Multicenter, Retrospective, Observational Study.
Journal: Journal of medical Internet research
Published: May 24, 2024
The Long-Term Uptake of Home Spirometry in Regular Cystic Fibrosis Care: Retrospective Multicenter Observational Study.
Journal: Journal of medical Internet research
Published: May 19, 2024
Potential, Pitfalls, and Future Directions for Remote Monitoring of Chronic Respiratory Diseases: Multicenter Mixed Methods Study in Routine Cystic Fibrosis Care.
Journal: Journal of medical Internet research
Published: November 28, 2023
Clinical validation of digital biomarkers for paediatric patients with asthma and cystic fibrosis: potential for clinical trials and clinical care.
Journal: The European respiratory journal
Published: January 23, 2021
Postdischarge Recovery after Acute Pediatric Lung Disease Can Be Quantified with Digital Biomarkers.
Postdischarge Recovery after Acute Pediatric Lung Disease Can Be Quantified with Digital Biomarkers.
Journal: Respiration; international review of thoracic diseases
Published: December 02, 2020
Technical validity and usability of a novel smartphone-connected spirometry device for pediatric patients with asthma and cystic fibrosis.
Journal: Pediatric pulmonology
Published: April 23, 2020
Pharmacokinetics and safety of tobramycin nebulization with the I-neb and PARI-LC Plus in children with cystic fibrosis: A randomized, crossover study.
Journal: British journal of clinical pharmacology
Published: January 21, 2019
Red blood cell distribution width is not a reliable biomarker for low iron stores in children with cystic fibrosis.
Journal: Pediatric hematology and oncology
Published: March 10, 2017
CT-abnormalities, bacteriology and symptoms of sinonasal disease in children with Cystic Fibrosis.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: November 30, 2015
The value of soluble transferrin receptor and hepcidin in the assessment of iron status in children with cystic fibrosis.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: December 03, 2013
Last Updated: 09/26/2026