Associated Papers
Genetic heterogeneity in patients with Bartter syndrome type 1.
Sun M et al.
Molecular Medicine Reports, 2017
Long-term follow-up of patients with Bartter syndrome type I and II.
Puricelli E et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2010
A thiazide test for the diagnosis of renal tubular hypokalemic disorders.
Colussi G et al.
Clinical Journal of the American Society of Nephrology : Cjasn, 2007
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome.
Reinalter SC et al.
Kidney International, 2002
Phenotypic variability in Bartter syndrome type I.
Bettinelli A et al.
Pediatric Nephrology (berlin, Germany), 2000
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