Oliver Wrong

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.

R. Thakker, C. Pusey, R. Unwin, 2001, Kidney international.

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis).

E. Hatchwell, S. Fisher, I. Craig, 1994, Human molecular genetics.

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

S. Fisher, I. Craig, S. Pearce, 1997, Human molecular genetics.

Urinary acidification assessed by simultaneous furosemide and fludrocortisone treatment: an alternative to ammonium chloride.

R. Unwin, O. Wrong, S. Walsh, 2007, Kidney international.

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.

S. Povey, M. Tanner, M. Burley, 1997, The Journal of clinical investigation.