"Hypercalciuria" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Excretion of abnormally high level of CALCIUM in the URINE, greater than 4 mg/kg/day.
| Descriptor ID |
D053565
|
| MeSH Number(s) |
C23.888.942.337
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hypercalciuria".
Below are MeSH descriptors whose meaning is more specific than "Hypercalciuria".
This graph shows the total number of publications written about "Hypercalciuria" by people in this website by year, and whether "Hypercalciuria" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypercalciuria" by people in Profiles.
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Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria. J Clin Endocrinol Metab. 2020 07 01; 105(7).
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ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. Hum Reprod. 2019 06 04; 34(6):1155-1164.
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An 8-year-old with genu valgum: Answers. Pediatr Nephrol. 2019 04; 34(4):621-624.
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Kidney Calculi: Pathophysiology and as a Systemic Disorder. Iran J Kidney Dis. 2017 May; 11(3):180-191.
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Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis. J Clin Endocrinol Metab. 2014 Nov; 99(11):E2451-6.
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Differences in metabolic urinary abnormalities in stone forming and nonstone forming patients with primary hyperparathyroidism. Surgery. 2012 Mar; 151(3):477-83.