User profiles for Coline H. M. van Moorsel

Coline van Moorsel

St Antonius ILD center of Excellence
Verified email at antoniusziekenhuis.nl
Cited by 6452

[HTML][HTML] Whole lung lavage therapy for pulmonary alveolar proteinosis: a global survey of current practices and procedures

…, J Grutters, K Nakata, CHM Van Moorsel… - Orphanet journal of rare …, 2016 - Springer
Background Whole lung lavage (WLL) is the current standard of care treatment for patients
affected by pulmonary alveolar proteinosis (PAP). However, WLL is not standardized and …

European Respiratory Society statement on familial pulmonary fibrosis

…, J van der Smagt, CHM van Moorsel - European …, 2023 - Eur Respiratory Soc
Genetic predisposition to pulmonary fibrosis has been confirmed by the discovery of several
gene mutations that cause pulmonary fibrosis. Although genetic sequencing of familial …

Long‐term expanding human airway organoids for disease modeling

…, EE Voest, CHM van Moorsel, CK van der Ent… - The EMBO …, 2019 - embopress.org
Organoids are self‐organizing 3D structures grown from stem cells that recapitulate essential
aspects of organ structure and function. Here, we describe a method to establish long‐term…

Genetic disorders of the surfactant system: focus on adult disease

CHM van Moorsel, JJ van der Vis… - European Respiratory …, 2021 - Eur Respiratory Soc
Genes involved in the production of pulmonary surfactant are crucial for the development
and maintenance of healthy lungs. Germline mutations in surfactant-related genes cause a …

[HTML][HTML] MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

…, CHM van Moorsel, J van der Vis… - … England Journal of …, 2018 - Mass Medical Soc
Background Given the phenotypic similarities between rheumatoid arthritis (RA)–associated
interstitial lung disease (ILD) (hereafter, RA-ILD) and idiopathic pulmonary fibrosis, we …

Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort

CHM van Moorsel, MFM van Oosterhout… - American journal of …, 2010 - atsjournals.org
Rationale: Familial clustering of adult idiopathic interstitial pneumonias (IIP) suggests that
genetic factors might play an important role in disease development. Mutations in the gene …

Methotrexate vs azathioprine in second-line therapy of sarcoidosis

…, M Veltkamp, M Thomeer, CHM van Moorsel… - Chest, 2013 - Elsevier
HM Deneer PhD b , Marcel Veltkamp MD, PhD a , Michiel Thomeer MD, PhD e , Coline HM
van Moorsel … Dr van Moorsel: contributed to data analysis and interpretation and manuscript …

Predicting outcomes in idiopathic pulmonary fibrosis using automated computed tomographic analysis

…, CHM Van Moorsel, HW Van Es… - American journal of …, 2018 - atsjournals.org
Rationale: Quantitative computed tomographic (CT) measures of baseline disease severity
might identify patients with idiopathic pulmonary fibrosis (IPF) with an increased mortality risk. …

[HTML][HTML] Serum and BALF YKL-40 levels are predictors of survival in idiopathic pulmonary fibrosis

NM Korthagen, CHM van Moorsel, NP Barlo… - Respiratory …, 2011 - Elsevier
BACKGROUND: The chitinase-like protein YKL-40 is a serum biomarker in diseases with
fibrosis, inflammation and tissue remodelling. Idiopathic pulmonary fibrosis (IPF) is a …

[HTML][HTML] Predicting outcomes in rheumatoid arthritis related interstitial lung disease

J Jacob, N Hirani, CHM Van Moorsel… - European …, 2019 - Eur Respiratory Soc
The aim of this study was to compare radiology-based prediction models in rheumatoid
arthritis-related interstitial lung disease (RAILD) to identify patients with a progressive fibrosis …