(Q27693302)

Schlingmann KP

series ordinal

2

1 reference

language of work or name

1 reference

October 2011

1 reference

1 October 2011

4 references

24 March 2019

22 April 2019

9 October 2019

29 May 2020

4 references

24 March 2019

22 April 2019

9 October 2019

26

1 reference

issue

10

1 reference

page(s)

1789-802

1 reference

https://scigraph.springernature.com/pub.10.1007/s00467-011-1871-4

exact match

0 references

cites work

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Macula densa sensing and signaling mechanisms of renin release

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Salt wasting and deafness resulting from mutations in two chloride channels

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

A new familial disorder characterized by hypokalemia and hypomagnesemia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Rare presentation of cystinosis mimicking Bartter's syndrome: reports of two patients and review of the literature

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Hereditary renal tubular disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

An improved terminology and classification of Bartter-like syndromes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Gitelman-like syndrome after cisplatin therapy: a case report and literature review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Hereditary polyuric disorders: new concepts and differential diagnosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Pharmacotyping of hypokalaemic salt-losing tubular disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Bartter and Gitelman syndromes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Bartter's syndrome. A review of 28 patients followed for 10 years

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Juxtaglomerular cell complex in the regulation of renal salt excretion.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Renal calcifications: a complication of long-term furosemide therapy in preterm infants.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Temporal adaptation of tubuloglomerular feedback: effects of COX-2.

2 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published e

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

"Bartter-like" phenotype in Kearns-Sayre syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Amikacin-induced type 5 Bartter-like syndrome with severe hypocalcemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Successful utilization of aliskiren, a direct renin inhibitor in Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Bartter syndrome: benefits and side effects of long-term treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Pathogenetic role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome: therapeutic use of the cyclooxygenase-2 inhibitor nimesulide

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1871-4

A syndrome resembling Bartter's syndrome in sarcoidosis

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163795

Functional Characterization of a Calcium-Sensing Receptor Mutation in Severe Autosomal Dominant Hypocalcemia with a Bartter-Like Syndrome

27 November 2018

1 reference

12 December 2020

Non-steroidal anti-inflammatory drug-associated nephrotoxicity in Bartter syndrome

1 reference

12 December 2020

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

12 December 2020

Long-term follow-up of patients with Bartter syndrome type I and II

1 reference

12 December 2020

Hypokalaemic alkalosis, acquired Gitelman's and Bartter's syndrome in chronic sialoadenitis

1 reference

12 December 2020

Gitelman's not-so-benign syndrome

1 reference

12 December 2020

Familial hypokalemia/hypomagnesemia and chondrocalcinosis

1 reference

12 December 2020

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

1 reference

12 December 2020

CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Total body potassium in Bartter's syndrome before and during treatment with enalapril

1 reference

12 December 2020

Pre-pubertal growth in the hyperprostaglandin E syndrome

1 reference

12 December 2020

Thiazide treatment of systemic hypertension: effects on serum magnesium and ventricular ectopic activity

1 reference

12 December 2020

Calcium homeostasis and hypercalciuria in hyperprostaglandin E syndrome

1 reference

12 December 2020

Chronic hypokalaemia of adults: Gitelman's syndrome is frequent but classical Bartter's syndrome is rare

1 reference

12 December 2020

Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome

1 reference

12 December 2020

Renal handling of water and sodium in infancy and childhood: A study using clearance methods during hypotonic saline diuresis

1 reference

12 December 2020

Bartter syndromes and other salt-losing tubulopathies

1 reference

12 December 2020

A thiazide test for the diagnosis of renal tubular hypokalemic disorders

1 reference

12 December 2020

Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes

1 reference

12 December 2020

Chronic hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism ("Bartter's syndrome"), and hypercalciuria. Report of two cases with emphasis on natural history and on catch-up growth during treatment

1 reference

12 December 2020

Correction of hypokalemia in Bartter's syndrome by enalapril

1 reference

12 December 2020

Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms

1 reference

12 December 2020

Immunolocalization of an inwardly rectifying K+ channel, K(AB)-2 (Kir4.1), in the basolateral membrane of renal distal tubular epithelia

1 reference

12 December 2020

New treatment options for Bartter's syndrome

1 reference

12 December 2020

Side-effects of long-term prostaglandin E(1) treatment in neonates

1 reference

12 December 2020