Nephrolithiasis-Diarrhoe-Syndrom

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Suzuki Y et al. (2008) Gain-of-function haplotype in the epithelial calcium channel TRPV6 is a risk factor for renal calcium stone formation.

Thorleifsson G et al. (2009) Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.

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Baggio B et al. (1986) An inheritable anomaly of red-cell oxalate transport in "primary" calcium nephrolithiasis correctable with diuretics.

Ljunghall S et al. (1979) Family history of renal stones in a population study of stone-formers and health subjects.

Smith LH et al. (1974) Acquired hyperoxaluria, urolithiasis, and intestinal disease: a new digestive disorder?

Resnick M et al. (1968) Genetic predisposition to formation of calcium oxalate renal calculi.

Marangella M et al. (1982) Hyperoxaluria in idiopathic calcium stone disease: further evidence of intestinal hyperabsorption of oxalate.

Robertson WG et al. (1980) The cause of idiopathic calcium stone disease: hypercalciuria or hyperoxaluria?

Cousin JL et al. (1976) The role of carbonic anhydrase inhibitors on anion permeability into ox red blood cells.