Cystic fibrosis and CFTR-related disorder with electrolyte imbalance at diagnosis: clinical features and outcome in an Italian cohort-Reference-Cited by-同舟云学术

Cystic fibrosis and CFTR-related disorder with electrolyte imbalance at diagnosis: clinical features and outcome in an Italian cohort

Published:2023-09-19 Issue:12 Volume:182 Page:5275-5283
ISSN:1432-1076
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Terlizzi Vito,Padoan Rita,Leonetti Giuseppina,Vitullo Pamela,Tosco Antonella,Taccetti Giovanni,Fevola Cristina,Ficili Francesca,Pepe Angela,Poli Piercarlo,Claut Laura,Daccò Valeria,Salvatore Donatello

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00431-023-05193-9.pdf

Reference33 articles.

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2. Shamsuddin AKM, Quinton PM (2019) Concurrent absorption and secretion of airway surface liquids and bicarbonate secretion in human bronchioles. Am J Physiol Lung Cell Mol Physiol 316:L953–L960

3. Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rock M, Rosenfeld M et al (2017) Diagnosis of cystic fibrosis: consensus guidelines from the cystic fibrosis foundation. J Pediatr 181S:S4-S15.e1

4. Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E, Sermet I, Schwarz M, Tzetis M, Wilschanski M et al (2011) Recommendations for the classification of diseases as CFTR-related disorders. J Cyst Fibros 10(Suppl 2):S86-102

5. Castellani C, De Boeck K, De Wachter E, Sermet-Gaudelus I, Simmonds NJ, Southern KW, ECFS (2022) Diagnostic Network Working Group. ECFS standards of care on CFTR-related disorders: updated diagnostic criteria. J Cyst Fibros 21:908–921