Recurrent Nephrolithiasis and Beyond: The Long Diagnostic Odyssey of a Case of CLDN16 Mutation. [PDF]
Bhuiyan AAN +4 more
europepmc +1 more source
A Novel SLC9A3R1 Mutation as a Rare Cause of Infantile Hypercalcemia. [PDF]
Ravi Kumar P +4 more
europepmc +1 more source
Tailored Kidney Stone Prevention Improves Metabolic Risk Factors and Reduces Renal Colic Rate. [PDF]
Van de Perre E +14 more
europepmc +1 more source
Low-Dose Indapamide vs. Hydrochlorothiazide in Idiopathic Hypercalciuria: A Randomized Prospective Trial. [PDF]
Peraire M +5 more
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Acute Kidney Injury Secondary to Vitamin D Intoxication: A Case of Oxalate Nephropathy. [PDF]
Prime M, Segamwenge I, Mousa A.
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Whole exome sequencing reveals a pathogenic homozygous CLDN16 mutation in a 17-year-old patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis: A case report. [PDF]
Wang F, Adeerjiang Y, Xing HQ, Jiang S.
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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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Genetic background of infantile hypophosphatemia: a narrative review. [PDF]
Zeng X, Hu L.
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Estimates of Urinary Calcium Excretion in Dogs With and Without Calcium Oxalate Urolithiasis. [PDF]
LaVine DE +4 more
europepmc +1 more source

