(Q46621341)

English

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations

scientific article published on 27 July 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

author name string

Ju Hyung Kang

1

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Hyun Jin Choi

2

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Hee Yeon Cho

3

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Joo Hoon Lee

4

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Il Soo Ha

5

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Hae Il Cheong

6

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Yong Choi

7

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

publication date

27 July 2005

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

20

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

10

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

1490-1493

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Magnesium transport in the renal distal convoluted tubule

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNC

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in molecular genetics of hereditary magnesium-losing disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal magnesium handling and its hormonal control

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomagnesaemia of hereditary renal origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of hereditary disorders of magnesium homeostasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

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/16047219

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/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Should dietary calcium and protein be restricted in patients with nephrolithiasis?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16047219

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-005-1969-7

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/16047219

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