Inherited forms of renal hypomagnesemia: an update (Q37279942)

19 August 2017

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title

Inherited forms of renal hypomagnesemia: an update (English)

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19 August 2017

Nine V A M Knoers

1

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19 August 2017

publication date

26 September 2008

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19 August 2017

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19 August 2017

volume

24

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19 August 2017

issue

4

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19 August 2017

page(s)

697-705

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Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure

19 August 2017

cites work

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12 December 2020

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

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12 December 2020

Pathophysiology of the renal acidification defect present in the syndrome of familial hypomagnesaemia-hypercalciuria

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12 December 2020

CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis

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12 December 2020

Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase gamma-subunit

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12 December 2020

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

1 reference

12 December 2020

Hypomagnesaemia-hypercalciuria-nephrocalcinosis: a report of nine cases and a review

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12 December 2020

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

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12 December 2020

Epithelial Ca2+ and Mg2+ channels in health and disease

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12 December 2020

The structural unit of the thiazide-sensitive NaCl cotransporter is a homodimer.

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12 December 2020

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

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12 December 2020

Isolated autosomal recessive renal magnesium loss in two sisters

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12 December 2020

TRP channels as cellular sensors

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12 December 2020

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

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12 December 2020

Apical enrichment of human EGF precursor in Madin-Darby canine kidney cells involves preferential basolateral ectodomain cleavage sensitive to a metalloprotease inhibitor

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12 December 2020

Human epidermal growth factor precursor: cDNA sequence, expression in vitro and gene organization

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12 December 2020

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

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12 December 2020

Mutations in the Na-Cl cotransporter reduce blood pressure in humans

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12 December 2020

Evidence for parathyroid failure in magnesium deficiency

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12 December 2020

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

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12 December 2020

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

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12 December 2020

Magnesium wasting associated with epidermal-growth-factor receptor-targeting antibodies in colorectal cancer: a prospective study

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12 December 2020

Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease

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12 December 2020

Genetic heterogeneity in familial renal magnesium wasting

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12 December 2020

Bioavailability of US commercial magnesium preparations

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12 December 2020

Paracellin-1 and the modulation of ion selectivity of tight junctions

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12 December 2020

The congenital "magnesium-losing kidney". Report of two patients

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12 December 2020

Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria and nephrocalcinosis in siblings

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12 December 2020

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

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12 December 2020

Renal magnesium wasting in two families with autosomal dominant inheritance

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12 December 2020

Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension

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12 December 2020

Clinical presentation and outcome in primary familial hypomagnesaemia

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12 December 2020

Na,K-ATPase from mice lacking the gamma subunit (FXYD2) exhibits altered Na+ affinity and decreased thermal stability

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12 December 2020

The gamma subunit modulates Na(+) and K(+) affinity of the renal Na,K-ATPase

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12 December 2020

Decreased bicarbonate threshold and renal magnesium wasting in a sibship with distal renal tubular acidosis. (Evaluation of the pathophysiological role of parathyroid hormone)

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12 December 2020

Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome

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12 December 2020

Hypomagnesaemia of hereditary renal origin

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12 December 2020

Hypomagnesemia and chondrocalcinosis in Bartter's and Gitelman's syndrome: review of the pathogenetic mechanisms

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Distribution of transcellular calcium and sodium transport pathways along mouse distal nephron

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12 December 2020

Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

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12 December 2020

Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands

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12 December 2020

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

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12 December 2020

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

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12 December 2020

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations

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12 December 2020

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

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12 December 2020

Primary hypomagnesemia with secondary hypocalcemia in an infant

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12 December 2020

Gitelman's syndrome: towards genotype-phenotype correlations?

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12 December 2020

Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit

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12 December 2020

TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption

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12 December 2020

Renal magnesium and phosphate wastage in a patient with hypercalciuria and nephrocalcinosis: effect of oral phosphorus and magnesium supplements.

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12 December 2020

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

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12 December 2020

Chronic renal failure, end-stage renal disease, and peritoneal dialysis in Gitelman's syndrome

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12 December 2020

Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome).

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12 December 2020

Transgenic RNAi depletion of claudin-16 and the renal handling of magnesium

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12 December 2020

A novel claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting

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12 December 2020

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

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12 December 2020

A new familial disorder characterized by hypokalemia and hypomagnesemia

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12 December 2020

10.1007/S00467-008-0968-X

Identifiers

DOI

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19 August 2017

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