(Q46878905)

English

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentations

scientific article published in June 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentations (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

1 reference

based on heuristic

inferred from title

author name string

Hilary H Seeley

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

Lindsey A Loomba-Albrecht

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

Mato Nagel

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

Lavjay Butani

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

Andrew A Bremer

5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

publication date

1 June 2011

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

World Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

8

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

177-180

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

https://scigraph.springernature.com/pub.10.1007/s12519-011-0295-3

0 references

Tight junction biology and kidney dysfunction

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

Disease-associated mutations affect intracellular traffic and paracellular Mg2+ transport function of Claudin-16

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

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/10.1007%2FS12519-011-0295-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

Clinical presentation and outcome in primary familial hypomagnesaemia

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS12519-011-0295-3

21 January 2018

Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/21633858

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21633858

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21633858

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12519-011-0295-3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/21633858

ResearchGate publication ID

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