Neonates with Bartter syndrome have enormous fluid and sodium requirements
Author:
Affiliation:
1. Department of Pediatrics; Division of Pediatric Nephrology; Lausanne University Hospital; Lausanne Switzerland
2. Department of Pediatrics; Division of Pediatric Nephrology; Robert Debré University Hospital; Paris France
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Reference14 articles.
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2. Salt wasting and deafness resulting from mutations in two chloride channels;Schlingmann;N Engl J Med,2004
3. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome;Konrad;J Am Soc Nephrol,2000
4. Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes;Konrad;Pediatrics,1999
5. Prostaglandin E receptors and the kidney;Breyer;Am J Physiol Renal Physiol,2000
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