(Q81084066)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

[Familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Association with ocular abnormalities] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

author name string

C Loris Pablo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

C Martín de Vicente

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

S Abio Albero

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

M Justa Roldán

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

C Ferrer Novella

5

1 reference

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5 January 2020

publication date

1 December 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

Anales de Pediatria Continuada

5 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

volume

61

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

issue

6

1 reference

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5 January 2020

page(s)

502-508

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

Recent advances in molecular genetics of hereditary magnesium-losing disorders

5 January 2020

cites work

1 reference

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7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Hypomagnesemia due to renal disease of unknown etiology

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Hypomagnesaemia of hereditary renal origin

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7 January 2021

Renal magnesium wasting with hypercalciuria, nephrocalcinosis and ocular disorders

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

https://api.crossref.org/works/10.1016%2FS1695-4033%2804%2978436-2

7 January 2021

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

1 reference

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7 January 2021

Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNC

1 reference

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7 January 2021

Long-term outcome of paediatric patients with hereditary tubular disorders

1 reference

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7 January 2021

A deletion of the paracellin-1 gene is responsible for renal tubular dysplasia in cattle.

1 reference

https://api.crossref.org/works/10.1016%2FS1695-4033%2804%2978436-2

7 January 2021

Null mutation of PCLN-1/Claudin-16 results in bovine chronic interstitial nephritis

1 reference

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7 January 2021

Genetic disorders of magnesium homeostasis

1 reference

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7 January 2021

Randomized double-blind study of potassium citrate in idiopathic hypocitraturic calcium nephrolithiasis

1 reference

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7 January 2021

Great strides in the understanding of renal magnesium and calcium reabsorption

1 reference

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7 January 2021

10.1016/S1695-4033(04)78436-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15574250%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference