Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail [PDF]
, 2006 Dominik Müller +3 more
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Reduction of hypercalciuria in tetraplegia after weight-bearing and strengthening exercises [PDF]
, 1981 Paul E. Kaplan +4 more
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The Most Important Metabolic Risk Factors in Recurrent Urinary Stone Formers
Urology Journal, 2011 PURPOSE: To evaluate different urinary factors contributing to idiopathiccalcium stone disease for determining appropriate medical treatments.MATERIALS AND METHODS: Two 24-hour urine samples were collectedfrom 106 male recurrent idiopathic calcium stone ...
Mohaddeseh Azadvari +7 more
doaj
Clinical features and genetic analysis of 15 Chinese children with dent disease
Renal FailureObjective The clinical characteristics, genetic mutation spectrum, treatment strategies and prognoses of 15 children with Dent disease were retrospectively analyzed to improve pediatricians’ awareness of and attention to this disease.Methods We ...
Qian Li +8 more
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Hypercalciuria in a patient with central diabetes insipidus [PDF]
, 2013 Alexandros Ginis +1 more
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Deletion of claudin-10 rescues claudin-16–deficient mice from hypomagnesemia and hypercalciuria [PDF]
, 2017 Tilman Breiderhoff +8 more
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JCRPEHereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare fibroblast growth factor-23-independent disorder caused by biallelic variants in the SLC34A3 gene.
Luciana Pinto Valadares +1 more
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Hypercalciuria following ceftriaxone a fact or myth.
, 2015 Anoush Azarfar +7 more
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Evaluation of the calcium-sensing receptor gene in idiopathic hypercalciuria and calcium nephrolithiasis [PDF]
, 2000 Martin Petrucci +7 more
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