Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutation-Reference-Cited by-同舟云学术

Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutation

Published:2004-06 Issue:2 Volume:3 Page:135-136
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Salvatore Donatello,Tomaiuolo Rossella,Abate Rosaria,Vanacore Borghina,Manieri Sergio,Mirauda Maria Pia,Scavone Amelia,Schiavo Maria Vittoria,Castaldo Giuseppe,Salvatore Francesco

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Hypoelectrolytemia and metabolic alkalosis in infants with cystic fibrosis;Beckerman;Pediatrics,1979

2. Cystic fibrosis with acute hypoelectrolytemia and metabolic alkalosis in infancy;Nussbaum;Am. J. Dis. Child,1979

3. Cystic fibrosis mimicking Bartter's syndrome;Davison;Acta Paediatr. Scand.,1983

4. Cystic fibrosis revealed by dehydration with hypochloronatremic alkalosis in 3 infants and a neonate;Berard;Arch. Pediatr.,1994

5. Chloride deficiency as a presentation or complication of cystic fibrosis;Sojo;Eur. J. Pediatr.,1994

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