A boy with congenital analbuminemia and steroid-sensitive idiopathic nephrotic syndrome: an experiment of nature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-007-0620-y.pdf
Reference24 articles.
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2. Boner G, Cox AJ, Kelly DJ, Tobar A, Bernheim J, Langham RG, Cooper ME, Gilbert RE (2003) Does vascular endothelial growth factor (VEGF) play a role in the pathogenesis of minimal change disease? Nephrol Dial Transplant 18:2293–2299
3. Brocklebank T, Cooper EH, Richmond K (1991) Sodium dodecyl sulphate polyacrylamide gel electrophoresis patterns of proteinuria in various renal diseases of childhood. Pediatr Nephrol 5:371–375
4. Campagnoli M, Sala A, Labo S, Rossi A, Neuhaus TJ, Braegger CP, Minchiotti L, Galliano M (2005) Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. Clin Biochem 38:819–823
5. Deschênes G, Guigonis V, Doucet A (2004) Molecular mechanism of edema formation in nephrotic syndrome. Arch Pediatr 11:1084–1094
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