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Results: 1-8 |
Results: 8
Glomerular protein sieving and implications for renal failure in Fanconi syndrome
Authors: Norden, AGW Lapsley, M Lee, PJ Pusey, CD Scheinman, SJ Tam, FWK Thakker, RV Unwin, RJ Wrong, O
Citation: Agw. Norden et al., Glomerular protein sieving and implications for renal failure in Fanconi syndrome, KIDNEY INT, 60(5), 2001, pp. 1885-1892
Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosisin Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells (vol 350, pg 41, 2000)
Authors: Bruce, LJ Wrong, O Toye, AM Young, MT Ogle, G Ismail, Z Sinha, AK McMaster, P Hwaihwanje, I Nash, GB Hart, S Lavu, E Palmer, R Othman, A Unwin, RJ Tanner, MJA
Citation: Lj. Bruce et al., Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosisin Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells (vol 350, pg 41, 2000), BIOCHEM J, 351, 2000, pp. 839-839
Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosisin Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells
Authors: Bruce, LJ Wrong, O Toye, AM Young, MT Ogle, G Ismail, Z Sinha, AK McMaster, P Hwaihwanje, I Nash, GB Hart, S Lavu, E Palmer, R Othman, A Unwin, RJ Tanner, MJA
Citation: Lj. Bruce et al., Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosisin Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells, BIOCHEM J, 350, 2000, pp. 41-51
Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria
Authors: Scheinman, SJ Cox, JPD Lloyd, SE Pearce, SHS Salenger, PV Hoopes, RR Bushinsky, DA Wrong, O Asplin, JR Langman, CB Norden, AGW Thakker, RV
Citation: Sj. Scheinman et al., Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria, KIDNEY INT, 57(1), 2000, pp. 232-239
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases
Authors: Norden, AGW Scheinman, SJ Deschodt-Lanckman, MM Lapsley, M Nortier, JL Thakker, RV Unwin, RJ Wrong, O
Citation: Agw. Norden et al., Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases, KIDNEY INT, 57(1), 2000, pp. 240-249
Renal chloride channel, CLCN5, mutations in Dent's disease
Authors: Cox, JPD Yamamoto, K Christie, PT Wooding, C Feest, T Flinter, FA Goodyer, PR Leumann, E Neuhaus, T Reid, C Williams, PF Wrong, O Thakker, RV
Citation: Jpd. Cox et al., Renal chloride channel, CLCN5, mutations in Dent's disease, J BONE MIN, 14(9), 1999, pp. 1536-1542
Amelogenesis imperfecta, nephrocalcinosis, and hypocalciuria syndrome in two siblings from a large family with consanguineous parents
Authors: Dellow, EL Harley, KE Unwin, RJ Wrong, O Winter, GB Parkins, BJ
Citation: El. Dellow et al., Amelogenesis imperfecta, nephrocalcinosis, and hypocalciuria syndrome in two siblings from a large family with consanguineous parents, NEPH DIAL T, 13(12), 1998, pp. 3193-3196
The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) gene
Authors: Bruce, LJ Unwin, RJ Wrong, O Tanner, MJA
Citation: Lj. Bruce et al., The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) gene, BIOC CELL B, 76(5), 1998, pp. 723-728
Risultati: 1-8 |