Ghent University Academic Bibliography

Journal Article

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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Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND) : an open-label extension study

Patrick A Flume, Reta Fischer Biner, Damian G Downey, Cynthia Brown, Manu Jain, Rainald Fischer, Kris De Boeck, Gregory S Sawicki, Philip Chang, Hildegarde Paz-Diaz, et al.

(2021) LANCET RESPIRATORY MEDICINE. 9(7). p.733-746

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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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A method for comprehensive proteomic analysis of human faecal samples to investigate gut dysbiosis in patients with cystic fibrosis

Griet Debyser (UGent) , Maarten Aerts, Pieter Van Hecke, Bart Mesuere (UGent) , Gwen Duytschaever (UGent) , Peter Dawyndt (UGent) , Kris De Boeck, Peter Vandamme (UGent) and Bart Devreese (UGent)

(2019) ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY. 1073. p.137-160

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Journal Article
A1
open access

CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trials

Scott C. Bell, Peter J. Barry, Kris De Boeck, Pavel Drevinek, J. Stuart Elborn, Barry J. Plant, Predag Minić, Eva Van Braeckel (UGent) , Stijn Verhulst, Karine Muller, et al.

(2019) JOURNAL OF CYSTIC FIBROSIS. 18(5). p.700-707

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Faecal proteomics : a tool to investigate dysbiosis and inflammation in patients with cystic fibrosis

Griet Debyser (UGent) , Bart Mesuere (UGent) , Lieven Clement (UGent) , Jens Van de Weygaert (UGent) , Pieter Van Hecke, Gwen Duytschaever (UGent) , Maarten Aerts (UGent) , Peter Dawyndt (UGent) , Kris De Boeck, Peter Vandamme (UGent) , et al.

(2016) JOURNAL OF CYSTIC FIBROSIS. 15(2). p.242-250

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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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Amoxicillin-clavulanic acid resistance in fecal Enterobacteriaceae from patients with cystic fibrosis and healthy siblings

Gwen Duytschaever (UGent) , Geert Huys (UGent) , Linda Boulanger, Kris De Boeck and Peter Vandamme (UGent)

(2013) JOURNAL OF CYSTIC FIBROSIS. 12(6). p.780-783

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Journal Article
A1
open access

Dysbiosis of bifidobacteria and Clostridium cluster XIVa in the cystic fibrosis fecal microbiota

Gwen Duytschaever (UGent) , Geert Huys (UGent) , Maarten Bekaert (UGent) , Linda Boulanger, Kris De Boeck and Peter Vandamme (UGent)

(2013) JOURNAL OF CYSTIC FIBROSIS. 12(3). p.206-215

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Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome

Heidi Schaballie (UGent) , Marleen Renard, Christiane Vermylen, Isabelle Scheers, Nicole Revencu, Luc Regal, David Cassiman, Lieve Sevenants, Ilse Hoffman, Anniek Corveleyn, et al.

(2013) EUROPEAN JOURNAL OF PEDIATRICS. 172(5). p.613-622

Academic Bibliography

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

Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND) : an open-label extension study

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

A method for comprehensive proteomic analysis of human faecal samples to investigate gut dysbiosis in patients with cystic fibrosis

CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trials

Faecal proteomics : a tool to investigate dysbiosis and inflammation in patients with cystic fibrosis

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

Amoxicillin-clavulanic acid resistance in fecal Enterobacteriaceae from patients with cystic fibrosis and healthy siblings

Dysbiosis of bifidobacteria and Clostridium cluster XIVa in the cystic fibrosis fecal microbiota

Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome

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