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Résultats de la recherche - 6 results
The effect of enteral tube feeding in cystic fibrosis: A registry based study.
gezondheid in kaart brengen Health and disease monitoring Manuscript versions: DOI: https://doi.org/10.1016/j.jcf.2018.01.004 File: Version: Published Full text access: Public Access Full text language: ...
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
in CF-disease liability is hardly documented. METHODS: Belgian CF-Registry 2013 data were analyzed to identify CF with at least 1 RM (CF + RM). Clinical data and sweat chloride of CF + RM were compared ...
Ethnicity impacts the cystic fibrosis diagnosis: A note of caution.
Publication Type: Peer reviewed scientific article Authors: Bosch, Barbara; Bilton, Diana; Sosnay, Patrick; Raraigh, Karen S; Mak, Denise Y F; Ishiguro, Hiroshi; Gulmans, Vincent; Muriel Thomas; Cuppens, Harry; Amaral, Margarida; De Boeck, Kris Source: J ...
Does newborn screening influence the young cystic fibrosis cohort included in national registries?
Publication Type: Peer reviewed scientific article Authors: De Boeck, Kris; Munck, Anne; de Monestrol, Isabelle; Gulmans, Vincent; Lemonnier, Lydie; Middleton, Peter G; Simeon Wanyama; Muriel Thomas Source: Eur Respir J, Volume 49, Issue 1 (2017) Health T ...
Treatment burden in patients with at least one class IV or V CFTR mutation
Index Young adult Abstract: CFTR mutations are grouped according to disease-causing mechanism. Several studies demonstrated that patients having at least one mutation of class IV /V, present with a milder ...
Is there evidence for correct diagnosis in cystic fibrosis registries?
registries. Excluding these patients for analyses leads to significant changes in outcomes. Health Topics: Health and disease monitoring Mucoviscidosis Surveillance de la santé et des maladies Ziekten en ...