Genetic causes of hypercalciuric nephrolithiasis. (17/112)

A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIc. (18/112)

Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunction. (19/112)

RANKL is a mediator of bone resorption in idiopathic hypercalciuria. (20/112)

Nephrolithiasis. (21/112)

Evidence for increased postprandial distal nephron calcium delivery in hypercalciuric stone-forming patients. (22/112)

NHERF1 mutations and responsiveness of renal parathyroid hormone. (23/112)

Salt and acid-base metabolism in claudin-16 knockdown mice: impact for the pathophysiology of FHHNC patients. (24/112)

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