Résultats de la recherche - 8 results

What can the CF registry tell us about rare CFTR-mutations? A Belgian study.

(0.1-2,0) (p < 0.0001)], lower sweat chloride [96 mmol/L (64-107) vs. 104 mmol/L (97-115) (p < 0.0001)], higher FEV1 %pred [77%pred (58-96) vs. 68%pred (48-86) (p = 0.017)], were less frequently ...

Ethnicity impacts the cystic fibrosis diagnosis: A note of caution.

Cuppens, Harry; Amaral, Margarida; De Boeck, Kris Source: J Cyst Fibros, Volume 16, Issue 4, p.488-491 (2017) Abstract: BACKGROUND: The diagnosis of Cystic Fibrosis (CF) is by consensus based on the same ...

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 ...

Treatment burden in patients with at least one class IV or V CFTR mutation

Publication Type: Peer reviewed scientific article Authors: Dewulf, Jonas; Vermeulen, François; Simeon Wanyama; Muriel Thomas; Proesmans, Marijke; Dupont, Lieven; De Boeck, Kris Source: Pediatr ...

Annual Report Belgian Cystic Fibrosis Registry 2013.

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Simeon Wanyama; Muriel Thomas; Malfroot,A. Source: WIV-ISP, Number 84, Brussels/Belgium, p.84 (2015) ISBN: ...

Jaarlijks Rapport Belgisch Mucoviscidose Register 2013.

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Simeon Wanyama; Muriel Thomas; Malfroot,A. Source: WIV-ISP, Number 84, Brussels/Belgium, p.84 (2015) ISBN: ...

Rapport Annuel Registre Belge de la Mucoviscidose 2013.

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Simeon Wanyama; Muriel Thomas; Malfroot,A. Source: WIV-ISP, Number 84, Brussels/Belgium, p.84 (2015) ISBN: ...

Is there evidence for correct diagnosis in cystic fibrosis registries?

predefined diagnostic criteria. RESULTS: Using as case definition sweat chloride >60mmol/L or 2 CFTR mutations identified, CF diagnosis was not documented in 2.8, 5.7, 6.5 and 21.6% of subjects in the F, B, ...

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