First retrospective study on pediatric nephrocalcinosis in Syria: clinical symptoms and causes. [PDF]
Ghanem H +3 more
europepmc +1 more source
A Challenging Case of Hypercalcemia Caused by a Novel Homozygous Variant Missense Mutation in the <i>CYP24A1</i> Gene. [PDF]
Ahsan T +4 more
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Beyond expensive innovations: affordable and effective strategies for managing tubulopathies in adults. [PDF]
Nielsen L, Figueres L.
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Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis. [PDF]
Cruz D, Pintassilgo I.
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Kidney-specific claudin-2 deficiency leads to medullary nephrocalcinosis in mice. [PDF]
Behm CV +15 more
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Nephrocalcinosis in a Child with Sotos Syndrome: A Case Report of Contiguous Gene Syndrome Encompassing <i>NSD1</i> and <i>SLC34A1</i> Genes. [PDF]
Bargenda-Lange A +5 more
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<i>CYP24A1</i> loss-of-function mutation as a rare cause of parathyroid (PTH)-independent severe hypercalcaemia in pregnancy. [PDF]
Morton A.
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