CLDN16Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis-Reference-Cited by-同舟云学术

CLDN16Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Published:2007-11-14 Issue:1 Volume:19 Page:171-181
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Konrad Martin,Hou Jianghui,Weber Stefanie,Dötsch Jörg,Kari Jameela A.,Seeman Tomas,Kuwertz-Bröking Eberhard,Peco-Antic Amira,Tasic Velibor,Dittrich Katalin,Alshaya Hammad O.,von Vigier Rodo O.,Gallati Sabina,Goodenough Daniel A.,Schaller André

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference42 articles.

1. Decreased bicarbonate threshold and renal magnesium wasting in a sibship with distal renal tubular acidosis

2. Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

3. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

4. Hypomagnesaemia–hypercalciuria–nephrocalcinosis: a report of nine cases and a review

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

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1. Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Family;Calcified Tissue International;2023-12-11

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5. Evaluation of Phenotypes and CLDN16 Variants in 2 Different Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Families: Phenotypic Differences in Siblings and Phenotypic Similarity in Monozygotic Twins;Turkish Journal of Nephrology;2023-01-04