Norden AG - Search Results

1

Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance.

Wrong OM, Norden AG, Feest TG. Wrong OM, et al. Among authors: norden ag. QJM. 1994 Aug;87(8):473-93. QJM. 1994. PMID: 7922301

2

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.

Pook MA, Wrong O, Wooding C, Norden AG, Feest TG, Thakker RV. Pook MA, et al. Among authors: norden ag. Hum Mol Genet. 1993 Dec;2(12):2129-34. doi: 10.1093/hmg/2.12.2129. Hum Mol Genet. 1993. PMID: 8111383

3

Oncogenic osteomalacia, raised FGF-23, and renal Fanconi syndrome.

Norden AG, Laing RJ, Rowe P, Unwin RJ, Wrong O, Crisp AJ. Norden AG, et al. QJM. 2014 Feb;107(2):139-41. doi: 10.1093/qjmed/hcr247. Epub 2011 Dec 16. QJM. 2014. PMID: 22179099 Free PMC article. No abstract available.

4

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.

Scheinman SJ, Cox JP, Lloyd SE, Pearce SH, Salenger PV, Hoopes RR, Bushinsky DA, Wrong O, Asplin JR, Langman CB, Norden AG, Thakker RV. Scheinman SJ, et al. Among authors: norden ag. Kidney Int. 2000 Jan;57(1):232-9. doi: 10.1046/j.1523-1755.2000.00774.x. Kidney Int. 2000. PMID: 10620204 Free article.

5

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.

Norden AG, Scheinman SJ, Deschodt-Lanckman MM, Lapsley M, Nortier JL, Thakker RV, Unwin RJ, Wrong O. Norden AG, et al. Kidney Int. 2000 Jan;57(1):240-9. doi: 10.1046/j.1523-1755.2000.00847.x. Kidney Int. 2000. PMID: 10620205 Free article.

6

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

Norden AG, Lapsley M, Lee PJ, Pusey CD, Scheinman SJ, Tam FW, Thakker RV, Unwin RJ, Wrong O. Norden AG, et al. Kidney Int. 2001 Nov;60(5):1885-92. doi: 10.1046/j.1523-1755.2001.00016.x. Kidney Int. 2001. PMID: 11703607 Free article.

7

X-linked recessive nephrolithiasis with renal failure.

Wrong O, Norden AG, Feest TG. Wrong O, et al. Among authors: norden ag. N Engl J Med. 1992 Apr 9;326(15):1029-30. doi: 10.1056/NEJM199204093261516. N Engl J Med. 1992. PMID: 1372109 No abstract available.

8

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.

Norden AG, Lapsley M, Lee PJ, Pusey CD, Scheinman SJ, Tam FW, Thakker RV, Unwin RJ, Wrong O. Norden AG, et al. Kidney Int. 2002 Jul;62(1):349. doi: 10.1046/j.1523-1755.2002.t01-1-00290.x. Kidney Int. 2002. PMID: 12081599 Free article. No abstract available.

9

In memoriam: Oliver M. Wrong.

Scheinman SJ, Feehally J, Feest TG, Norden AG, Thakker RV, Unwin RJ. Scheinman SJ, et al. Among authors: norden ag. Kidney Int. 2012 Jul;82(2):121-2. doi: 10.1038/ki.2012.183. Kidney Int. 2012. PMID: 22743559 Free article. No abstract available.

10

Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.

Norden AGW, Lapsley M, Igarashi T, Kelleher CL, Lee PJ, Matsuyama T, Scheinman SJ, Shiraga H, Sundin DP, Thakker RV, Unwin RJ, Verroust P, Moestrup SK. Norden AGW, et al. J Am Soc Nephrol. 2002 Jan;13(1):125-133. doi: 10.1681/ASN.V131125. J Am Soc Nephrol. 2002. PMID: 11752029

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