(Q40509794)

21 September 2017

title

Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study (English)

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21 September 2017

Velibor Tasic

1

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21 September 2017

Donco Dervisov

2

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21 September 2017

Svetlana Koceva

3

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21 September 2017

Stefanie Weber

4

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21 September 2017

Martin Konrad

5

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21 September 2017

publication date

26 April 2005

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21 September 2017

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21 September 2017

volume

20

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21 September 2017

issue

7

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21 September 2017

page(s)

1003-1006

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

21 September 2017

cites work

1 reference

12 December 2020

Urinary phosphate/creatinine, calcium/creatinine, and magnesium/creatinine ratios in a healthy pediatric population.

1 reference

12 December 2020

Early hypomagnesemia, hypercalciuria and nephrocalcinosis: two cases in a family

1 reference

12 December 2020

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

1 reference

12 December 2020

Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene

1 reference

12 December 2020

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

12 December 2020

Familial hypomagnesemia-hypercalciuria in 2 siblings.

1 reference

12 December 2020

Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNC

1 reference

12 December 2020

Renal hypomagnesemia, hypercalciuria and nephrocalcinosis in a middle-aged man.

1 reference

12 December 2020

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

1 reference

12 December 2020

Recent advances in molecular genetics of hereditary magnesium-losing disorders

1 reference

12 December 2020

Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle

1 reference

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)

1 reference

12 December 2020

Predicting GFR in children and adults: a comparison of the Cockcroft-Gault, Schwartz, and modification of diet in renal disease formulas

1 reference

12 December 2020

Hypomagnesaemia of hereditary renal origin

1 reference

12 December 2020

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

1 reference

12 December 2020

The use of plasma creatinine concentration for estimating glomerular filtration rate in infants, children, and adolescents

1 reference

12 December 2020

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

12 December 2020

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

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12 December 2020

Inherited disorders of renal magnesium handling

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12 December 2020

Pseudotumor cerebri in a child with familial hypomagnesemia-hypercalciuria

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

10.1007/S00467-005-1853-5

Identifiers

DOI

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Dimensions Publication ID

21 September 2017

1017727227

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