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American Journal of Kidney Diseases
Volume 51, Issue 6
, Pages 875-876
, June 2008
The Renal Fanconi Syndromes: The Proper Study of Mankind is Man
References
- . The Renal Fanconi Syndrome. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kizler KW, Vogelstein B editor. The Metabolic and Molecular Basis of Inherited Disease. (ed 8). New York, NY: McGraw-Hill; 2001;p. 5023–5038
- . Urinary protein excretion pattern and renal expression of megalin and cubilin in nephropathic cystinosis. Am J Kidney Dis. 2008;51:893–903
- . Chloride channels and endocytosis: new insights from Dent's disease and ClC-5 knockout mice. Nephron Physiol. 2005;99:69–73
- . Mechanisms of disease: what can mouse models tell us about the molecular processes underlying Dent disease?. Nat Clin Pract Nephrol. 2007;3:449–455
- Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome. J Am Soc Nephrol. 2002;13:125–133
- Examination of megalin in renal tubular epithelium from patients with Dent disease. Pediatr Nephrol. 2004;19:612–615
- The normal kidney filters nephrotic levels of albumin retrieved by proximal tubule cells: retrieval is disrupted in nephrotic states. Kidney Int. 2007;71:504–513
PII: S0272-6386(08)00742-7
doi: 10.1053/j.ajkd.2008.04.003
© 2008 National Kidney Foundation, Inc. Published by Elsevier Inc All rights reserved.
« Previous
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American Journal of Kidney Diseases
Volume 51, Issue 6
, Pages 875-876
, June 2008
