Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening

Author:

Sermet-Gaudelus I.,Brouard J.,Audrézet M.-P.,Couderc Kohen L.,Weiss L.ORCID,Wizla N.,Vrielynck S.,LLerena K.,Le Bourgeois M.,Deneuville E.,Remus N.,Nguyen-Khoa T.,Raynal C.,Roussey M.,Girodon E.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference50 articles.

1. Le dépistage néonatal systématique de la mucoviscidose en France : état des lieux et perspectives après 5 ans de fonctionnement. http://www.has-sante.fr/portail/./2009-04/rapport.mucoviscidose_en_fr; accessed 25 November 2016.

2. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: cystic fibrosis foundation consensus report;Farrell;J Pediatr,2008

3. Diagnosis of cystic fibrosis after newborn screening: the Australasian experience – 20 years and five million babies later: a consensus statement from the Australasian Paediatric Respiratory Group;Massie;Pediatr Pulmonol,2005

4. Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis;Sermet-Gaudelus;Thorax,2010

5. Cystic fibrosis: terminology and diagnostic algorithms;De Boeck;Thorax,2006

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