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2011, Methods in molecular biology, ISBN 1617791164, Volume 741-742., 2 v.
Book
06/2007
Cystic fibrosis (CF) is one of the most frequent inherited mortal diseases in Caucasian population. Dysfunction in exocrine glands is described in CF patients,... 
Sweat test | DF508 mutation | Diferencia de potencial nasal | Electrólitos en sudor | Nasal potential difference | Fibrosis quística | Cystic fibrosis | Mutación DF508 | CFTR
Web Resource
Pediatric Clinics of North America, ISSN 0031-3955, 2016, Volume 63, Issue 4, pp. 599 - 615
Journal Article
Paediatric Respiratory Reviews, ISSN 1526-0542, 08/2019, Volume 31, pp. 12 - 14
NICE produced a guideline for the diagnosis and management of CF (NG78) in October 2017. This paper describes the process of producing the guideline and... 
Cystic fibrosis | NICE guideline | Care and treatment | Diagnosis
Journal Article
Journal Article
Lancet, The, ISSN 0140-6736, 2009, Volume 373, Issue 9678, pp. 1891 - 1904
Journal Article
Diabetes Care, ISSN 0149-5992, 12/2010, Volume 33, Issue 12, pp. 2697 - 2708
Journal Article
Medical sciences (Basel, Switzerland), ISSN 2076-3271, 02/2019, Volume 7, Issue 2, p. 32
Chronic rhinosinusitis (CRS) is nearly ubiquitous in patients with cystic fibrosis (CF). CF CRS is a challenging entity to define, diagnose, and treat, as... 
diagnosis | rhinosinusitis | cystic fibrosis | medical management
Journal Article
Journal of Cystic Fibrosis, ISSN 1569-1993, 2017, Volume 16, pp. S17 - S17
Journal Article
Journal Article