Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment.

scientific article published on 14 April 2010

Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.JPEDS.2010.02.025
P698PubMed publication ID20394945
P5875ResearchGate publication ID43159482

P50authorAgnès LinglartQ57050654
P2093author name stringMinh Nguyen
Frederic Jehan
Huguette Guillozo
Eric Mallet
Michele Garabedian
Henri Boutignon
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectvitamin DQ175621
P304page(s)296-302
P577publication date2010-04-14
P1433published inThe Journal of PediatricsQ7743611
P1476titleInfantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment
P478volume157

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cites work (P2860)
Q367335701,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis
Q3591645825-Hydroxyvitamin D Can Interfere With a Common Assay for 1,25-Dihydroxyvitamin D in Vitamin D Intoxication
Q47126125A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 Pathway
Q39230407A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up
Q37616864A lifetime of hypercalcemia and hypercalciuria, finally explained
Q51092138CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations.
Q24634055Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemia
Q64066212Hereditary Hypercalcemia Caused by a Homozygous Pathogenic Variant in the Gene: A Case Report and Review of the Literature
Q50209902Hypercalcemia: a consultant's approach
Q88209215Hyperphosphatemic tumoral calcinosis caused by FGF23 compound heterozygous mutations: what are the therapeutic options for a better control of phosphatemia?
Q38616346Idiopathic infantile hypercalcemia: case report and review of the literature.
Q37265269Medullary nephrocalcinosis in an adult patient with idiopathic infantile hypercalcaemia and a novel CYP24A1 mutation
Q51866686Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome.
Q42557653Take another CYP: confirming a novel mechanism for "idiopathic" hypercalcemia
Q64940667Three Sisters With Heterozygous Gene Variants of CYP24A1: Maternal Hypercalcemia, New-Onset Hypertension, and Neonatal Hypoglycemia.
Q36720877Transient Hypercalcemia in Preterm Infants: Insights Into Natural History and Laboratory Evaluation

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