An improved terminology and classification of Bartter-like syndromes (Q34807394)

4 August 2017

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title

An improved terminology and classification of Bartter-like syndromes (English)

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4 August 2017

author

Hannsjörg W. Seyberth

series ordinal

1

object named as

Hannsjörg W Seyberth

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4 August 2017

publication date

12 August 2008

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Nature Clinical Practice Nephrology

4 August 2017

published in

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4 August 2017

volume

4

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4 August 2017

issue

10

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4 August 2017

page(s)

560-567

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Salt handling in the distal nephron: lessons learned from inherited human disorders.

4 August 2017

cites work

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Molecular pathogenesis of Bartter's and Gitelman's syndromes.

21 January 2018

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Pharmacotyping of hypokalaemic salt-losing tubular disorders

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Bartter's and Gitelman's syndromes: their relationship to the actions of loop and thiazide diuretics

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Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes

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7 January 2021

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Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance

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Hereditary polyuric disorders: new concepts and differential diagnosis.

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Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

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Low urinary calcium excretion in Bartter's syndrome

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Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis

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7 January 2021

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

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A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

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7 January 2021

Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter

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7 January 2021

Variant of Bartter's syndrome with a distal tubular rather than loop of Henle defect

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7 January 2021

Distal nephron function in Bartter's syndrome: abnormal conductance to chloride in the cortical collecting tubule?

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7 January 2021

Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

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7 January 2021

A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis

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7 January 2021

Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome

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7 January 2021

Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders

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Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.

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Perinatal management of a preterm neonate affected by hyperprostaglandin E2 syndrome (HPS).

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The role of cyclooxygenases and prostanoid receptorsin furosemide-like salt losing tubulopathy: the hyperprostaglandin E syndrome

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7 January 2021

Dominant role of prostaglandin E2 EP4 receptor in furosemide-induced salt-losing tubulopathy: a model for hyperprostaglandin E syndrome/antenatal Bartter syndrome

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7 January 2021

An update on cyclooxygenase-2 expression and metabolites in the kidney

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Increased systolic blood pressure with rofecoxib in congenital furosemide-like salt loss.

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7 January 2021

Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome.

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A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism

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7 January 2021

Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle

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7 January 2021

A thiazide test for the diagnosis of renal tubular hypokalemic disorders

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7 January 2021

Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity

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7 January 2021

Gitelman's syndrome: towards genotype-phenotype correlations?

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7 January 2021

Salt wasting and deafness resulting from mutations in two chloride channels

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7 January 2021

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness

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7 January 2021

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K secretion

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7 January 2021

Barttin increases surface expression and changes current properties of ClC-K channels

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7 January 2021

Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na -K -2Cl- co-transporter

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7 January 2021

Can renal tubular hypokalemic disorders be accurately diagnosed on the basis of the diuretic response to thiazide?

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7 January 2021

Bartter syndromes and other salt-losing tubulopathies

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7 January 2021

A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia

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7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0912

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4 August 2017

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