Dent's disease. by Neild, G, Thakker, R, Unwin, R, Wrong, O

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22. by Pook, M, Wrong, O, Wooding, C, Norden, A, Feest, T, Thakker, R

THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22) by Thakker, R, Pook, M, Wooding, C, Norden, A, Feest, T, Wrong, O

MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11 by Thakker, R, Pang, J, Wooding, C, Scheinman, S, Wrong, O, Pook, M

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). by Fisher, S, Black, G, Lloyd, SE, Hatchwell, E, Wrong, O, Thakker, R, Craig, I

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE by Lloyd, S, Pearce, S, Fisher, S, Harding, B, Scheinman, S, Goodyer, P, Wrong, O, Craig, I, Thakker, R

Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis. by Lloyd, SE, Pearce, S, Thomson, A, Bianchi, M, Craig, I, Fisher, S, Scheinman, S, Wrong, O, Thakker, R

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases. by Norden, A, Scheinman, S, Deschodt-Lanckman, M, Lapsley, M, Nortier, J, Thakker, R, Unwin, R, Wrong, O

A CASE OF SARCOIDOSIS WITH CRYPTOCOCCAL MENINGITIS by Scadding, J, Olsen, E, Booth, C, Wrong, O, Steiner, R, Darrell, J, Warrell, D, Goodwin, J

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome. by Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O

Glomerular protein sieving and implications for renal failure in Fanconi syndrome. by Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. by Lloyd, SE, Gunther, W, Pearce, S, Thomson, A, Bianchi, M, Bosio, M, Craig, I, Fisher, S, Scheinman, S, Wrong, O, Jentsch, T, Thakker, R

Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene. by Norden, A, Asplin, J, Deschodt-Lanckman, M, Langman, C, Lapsley, M, Nortier, J, Scheinman, S, Thakker, R, Unwin, R, Wrong, O

Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients. by Gorvin, C, Wilmer, M, Piret, S, Harding, B, van den Heuvel, L, Wrong, O, Jat, P, Lippiat, J, Levtchenko, E, Thakker, R

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria. by Scheinman, S, Cox, J, Lloyd, SE, Pearce, S, Salenger, P, Hoopes, R, Bushinsky, D, Wrong, O, Asplin, JR, Langman, C, Norden, A, Thakker, R

Renal chloride channel, CLCN5, mutations in Dent's disease. by Cox, J, Yamamoto, K, Christie, P, Wooding, C, Feest, T, Flinter, F, Goodyer, P, Leumann, E, Neuhaus, T, Reid, C, Williams, P, Wrong, O, Thakker, R

A common molecular basis for three inherited kidney stone diseases. by Lloyd, SE, Pearce, S, Fisher, S, Steinmeyer, K, Schwappach, B, Scheinman, S, Harding, B, Bolino, A, Devoto, M, Goodyer, P, Rigden, S, Wrong, O, Jentsch, T, Craig, I, Thakker, R

OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability. by Shrimpton, A, Hoopes, R, Knohl, S, Hueber, P, Reed, A, Christie, P, Igarashi, T, Lee, P, Lehman, A, White, C, Milford, D, Sanchez, MR, Unwin, R, Wrong, O, Thakker, R, Scheinman, S