(Q37070196)

18 August 2017

1 reference

title

Hereditary etiologies of hypomagnesemia (English)

1 reference

18 August 2017

Amir Said Alizadeh Naderi

series ordinal

1

1 reference

PubMed ID

18227801

18 August 2017

Robert F Reilly

series ordinal

2

1 reference

18 August 2017

1 February 2008

1 reference

Nature Clinical Practice Nephrology

18 August 2017

1 reference

18 August 2017

4

1 reference

18 August 2017

80-89

1 reference

18 August 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1038/ncpneph0680

18 August 2017

0 references

cites work

Mg(2+)-dependent inward rectification of ROMK1 potassium channels expressed in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

A magnesium-deficient patient presenting with hypocalcemia and hyperphosphatemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

Intestinal absorption of magnesium from food and supplements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Renal magnesium handling: new insights in understanding old problems

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Extracellular calcium sensing and extracellular calcium signaling

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Magnesium transport in the cortical thick ascending limb of Henle's loop of the rabbit

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Magnesium transport in the renal distal convoluted tubule

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

The Mg2+ and Mg(2+)-nucleotide-regulated channel-kinase TRPM7.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Experimental human magnesium depletion

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Secretion and metabolic efficacy of parthyroid hormone in patients with severe hypomagnesemia

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Functional hypoparathyroidism and parathyroid hormone end-organ resistance in human magnesium deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Hypomagnesemia and the parathyroid hormone-vitamin D endocrine system in children with insulin-dependent diabetes mellitus: effects of magnesium administration

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

PTH and vitamin D responses during treatment of hypomagnesaemic hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

A case of Gitelman's syndrome with chondrocalcinosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Recent advances in molecular genetics of hereditary magnesium-losing disorders

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Genetics of hereditary disorders of magnesium homeostasis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

The human paracellin-1 gene (hPCLN-1): renal epithelial cell-specific expression and regulation

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Paracellular channels!

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Association of paracellin-1 with ZO-1 augments the reabsorption of divalent cations in renal epithelial cells

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Familial hypomagnesaemia--hypercalciuria leading to end-stage renal failure.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Incomplete Distal Renal Tubular Acidosis in Hypomagnesemia-Dependent Hypocalcemia

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Renal localization and function of the tight junction protein, claudin-19.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Renal magnesium wasting in two families with autosomal dominant inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Evidence for parathyroid failure in magnesium deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Clinical presentation and outcome in primary familial hypomagnesaemia

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Calcium-ion-sensing cell-surface receptors

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Magnesium deficiency in critical illness

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Diuretics, Serum and Intracellular Electrolyte Levels, and Ventricular Arrhythmias in Hypertensive Men

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Ciclosporin reduces paracellin-1 expression and magnesium transport in thick ascending limb cells

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Proton-pump inhibitors and hypomagnesemic hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Pathogenetic mechanisms of hypomagnesemia in alcoholic patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Hungry bone syndrome after surgical parathyroidectomy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Magnesium and diabetes: a review

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Unusual clinical presentation and possible rescue of a novel claudin-16 mutation

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0680

7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0680

1 reference

PubMed ID

18227801

Dimensions Publication ID

18 August 2017

0 references

1 reference

PubMed ID

18227801