An improved terminology and classification of Bartter-like syndromes

Kurtz I (1998) Molecular pathogenesis of Bartter's and Gitelman's syndromes. Kidney Int 54: 1396–1410

Seyberth HW et al. (1998) Hypokalemic tubular disorders: the hyperprostaglandin E syndrome and the Gitelman-Bartter syndrome. In Oxford Textbook of Clinical Nephrology, 1085–1093 (Eds Davidson AM. et al.) Oxford: Oxford University Press

Reinalter SJ et al. (2004) Pharmacotyping of hypokalaemic salt-losing tubular disorders. Acta Physiol Scand 181: 513–521

Unwin RC and Capasso G (2006) Bartter's and Gitelman's syndromes: their relationship to the actions of loop and thiazide diuretics. Curr Opin Pharmacol 6: 208–213

Simon DB and Lifton RP (1998) Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes. Curr Opin Cell Biol 10: 450–454

Hebert SC (2003) Bartter syndrome. Curr Opin Nephrol Hypertens 12: 527–532

Konrad M et al. (2000) Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol 11: 1449–1459

Jeck N et al. (2005) Salt handling in the distal nephron: lessons learned from inherited human disorders. Am J Physiol Regul Integr Comp Physiol 288: R782–R795

Krämer BK et al. (2008) Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance. Nat Clin Pract Nephrol 4: 38–46

Bichet DG (2006) Hereditary polyuric disorders: new concepts and differential diagnosis. Semin. Nephrol 26: 224–233

Bartter FC et al. (1962) Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med 33: 811–828

Gitelman HJ et al. (1966) A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 79: 221–235

Rudin A et al. (1984) Low urinary calcium excretion in Bartter's syndrome. N Engl J Med 310: 1190

Rudin A et al. (1988) Low urinary calcium excretion in Bartter's syndrome. Scand J Urol Nephrol 22: 35–39

Bianchetti MG et al. (1992) Calciuria in Bartter's and similar syndromes. Clin Nephrol 38: 338

Gill JR Jr et al. (1976) Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis. Am J Med 61: 43–51

Bartter FC et al. (1998) Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. J Am Soc Nephrol 9: 516–528

Jeck N et al. (2000) Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype. Pediatr Res 48: 754–758

Zelikovic I et al. (2003) A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes. Kidney Int 63: 24–32

Lin SH et al. (2004) Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter. Am J Kidney Dis 43: 304–312

Puschett JB et al. (1988) Variant of Bartter's syndrome with a distal tubular rather than loop of Henle defect. Nephron 50: 205–211

Sutton RA et al. (1992) Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome. Miner Electrolyte Metab 18: 43–51

Colussi G et al. (1992) Distal nephron function in Bartter's syndrome: abnormal conductance to chloride in the cortical collecting tubule? Am J Nephrol 12: 229–239

Peters M et al. (2002) Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. Am J Med 112: 183–190

Fanconi A et al. (1971) Chronic hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism (“Bartter's syndrome”), and hypercalciuria: report of two cases with emphasis on natural history and catch-up growth during treatment [German]. Helv Paediatr Acta 26: 144–163

McCredie DA et al. (1971) Potassium-losing nephropathy of childhood. Med J Aust 16: 129–135

McCredie DA et al. (1974) Hypercalciuria in potassium-losing nephropathy: a variant of Bartter's syndrome. Aust Paediatr J 10: 286–295

Ohlsson A et al. (1984) A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis [Swedish]. Acta Paediatr Scand 73: 868–874

Seyberth HW et al. (1985) Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome. J Pediatr 107: 694–701

Seyberth HW et al. (1987) Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders. Pediatr Nephrol 1: 491–497

Konrad M et al. (1999) Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes. Pediatrics 103: 678–683

Kömhoff M et al. (2005) Perinatal management of a preterm neonate affected by hyperprostaglandin E2 syndrome (HPS) [Swedish]. Acta Paediatr 94: 1690–1693

Nüsing RM and Seyberth HW (2004) The role of cyclooxygenases and prostanoid receptors in furosemide-like salt losing tubulopathy: the hyperprostaglandin E syndrome. Acta Physiol Scand 181: 523–528

Nüsing RM et al. (2005) Dominant role of prostaglandin E2 EP4 receptor in furosemide-induced salt-losing tubulopathy: a model for hyperprostaglandin E syndrome/antenatal Bartter syndrome. J Am Soc Nephrol 16: 2354–2362

Harris RC (2008) An update on cyclooxygenase-2 expression and metabolites in the kidney. Curr Opin Nephrol Hypertens 17: 64–69

Kömhoff M et al. (2006) Increased systolic blood pressure with rofecoxib in congenital furosmide-like salt loss. Nephrol Dial Transplant 21: 1833–1837

Colussi G et al. (1994) Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome. Am J Nephrol 14: 127–135

Landau D (2006) Potassium-related inherited tubulopathies. Cell Mol Life Sci 63: 1962–1968

Nozu K et al. (2007) A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism. Pediatr Nephrol 22: 1219–1223

Köckerling A et al. (1996) Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle. J Pediatr 129: 519–528

Colussi G et al. (2007) A thiazide test for the diagnosis of renal tubular hypokalemic disorders. Clin J Am Soc Nephrol 2: 454–460

Kaissling B et al. (1985) Structural adaptation of the distal convoluted tubule to prolonged furosemide treatment. Am J Physiol 248: F374–F381

Cantone A et al. (2008) Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity. Am J Physiol Renal Physiol 294: F1366–F1372

Riveira-Munoz E et al. (2007) Gitelman's syndrome: towards genotype-phenotype correlations? Pediatr Nephrol 22: 326–332

Schlingmann KP et al. (2004) Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med 350: 1314–1319

Nozu K et al. (2008) Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med Genet 45: 182–186

Estévez R et al. (2001) Barttin is a Cl-channel β-subunit crucial for renal Cl-reabsorption and inner ear K+ secretion. Nature 414: 558–561

Waldegger S et al. (2002) Barttin increases surface expression and changes current properties of ClC-K channels. Pflugers Arch 444: 411–418

Pressler CA et al. (2006) Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl− co-transporter. J Am Soc Nephrol 17: 2136–2142

Sassen M et al. (2007) Can renal tubular hypokalemic disorders be accurately diagnosed on the basis of diuretic response to thiazide? Nat Clin Pract Nephrol 3: 528–529

Kleta R and Bockenhauer D (2006) Bartter syndromes and other salt-losing tubulopathies. Nephron Physiol 104: 73–80

Phillips DR et al. (2006) A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia. Nat Clin Pract Nephrol 2: 340–346