Ghent University Academic Bibliography

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Airway remodeling in cystic fibrosis is heterogeneous

Astrid Vermaut, Vincent Geudens, Lynn Willems, Gitte Aerts, Pieterjan Kerckhof, Charlotte Hooft, Hanne Beeckmans, Janne Kaes, Xin Jin, Charlotte De Fays, et al.

(2025) ANNALS OF THE AMERICAN THORACIC SOCIETY. 22(4).
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Rectal organoid morphology analysis (ROMA) as a novel physiological assay for diagnostic classification in cystic fibrosis

Senne Cuyx, Anabela Santo Ramalho, Steffen Fieuws, Nikky Corthout, Marijke Proesmans, Mieke Boon, Kaline Arnauts, Marianne S Carlon, Sebastian Munck, Lieven Dupont, et al.

(2024) THORAX. 79(9). p.834-841
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- Journal Article
- A1
- open access
Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversity

Cédric Lood, Charlotte Peeters (UGent) , Quentin Lamy-Besnier, Jeroen Wagemans, Daniel De Vos, Marijke Proesmans, Jean-Paul Pirnay, Fedoua Echahidi, Denis Piérard, Matthieu Thimmesch, et al.

(2021) PLOS PATHOGENS. 17(3).
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Chest CT scoring for evaluation of lung sequelae in congenital diaphragmatic hernia survivors

Emma Beel (UGent) , Stein M. Aukland, Mieke Boon, François Vermeulen, Anne Debeer and Marijke Proesmans

(2020) PEDIATRIC PULMONOLOGY. 55(3). p.740-746
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Defining polysaccharide antibody deficiency : measurement of anti-pneumococcal antibodies and anti-Salmonella typhi antibodies in a cohort of patients with recurrent infections

Giorgia Bucciol, Heidi Schaballie (UGent) , Rik Schrijvers, Barbara Bosch, Marijke Proesmans, Kris De Boeck, Mieke Boon, François Vermeulen, Natalie Lorent, Doreen Dillaerts, et al.

(2020) JOURNAL OF CLINICAL IMMUNOLOGY. 40(1). p.105-113
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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

Mieke Boone (UGent) , Anne Smits (UGent) , Harry Cuppens, Martine Jaspers, Marijke Proesmans, Lieven J Dupont, François L Vermeulen, Sabine Van daele (UGent) , Anne Malfroot, Veronique Godding, et al.

(2014) ORPHANET JOURNAL OF RARE DISEASES. 9.
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Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver disease

Peter Wittes, Louis Libbrecht (UGent) , Tania Roskams, Kris De Boeck, Lieven Dupont, Marijke Proesmans, Francois Vermeulen, Birgitta Strandvik, Anders Lindblad, Xavier Stephenne, et al.

(2011) HEPATOLOGY. 53(3). p.1064-1065

Academic Bibliography

Airway remodeling in cystic fibrosis is heterogeneous

Rectal organoid morphology analysis (ROMA) as a novel physiological assay for diagnostic classification in cystic fibrosis

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

Chest CT scoring for evaluation of lung sequelae in congenital diaphragmatic hernia survivors

Defining polysaccharide antibody deficiency : measurement of anti-pneumococcal antibodies and anti-Salmonella typhi antibodies in a cohort of patients with recurrent infections

Primary ciliary dyskinesia : critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure

Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver disease

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