A Novel SLC9A3R1 Mutation as a Rare Cause of Infantile Hypercalcemia. [PDF]
Ravi Kumar P +4 more
europepmc +1 more source
Clinical Approaches and Emerging Therapeutic Horizons in Primary Hyperoxaluria. [PDF]
Martínez-Galindo R +7 more
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Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case Series. [PDF]
Turan I +12 more
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Gitelman Syndrome With Two Variants of Uncertain Significance: A Case Report. [PDF]
Bragança R +3 more
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Genetic causes of nephrolithiasis and nephrocalcinosis in a pediatric population in Saudi Arabia. [PDF]
Alsubaie H +8 more
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The domestic pig as a translational model of hyperoxaluria: a pilot study of acute and chronic sodium oxalate infusion. [PDF]
Jacek T +10 more
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Ten tips on the work-up and management of CKD patients with nephrolithiasis. [PDF]
Hawkins-van der Cingel G.
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Recurrent Nephrolithiasis and Beyond: The Long Diagnostic Odyssey of a Case of CLDN16 Mutation. [PDF]
Bhuiyan AAN +4 more
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