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Title

Urinary low-molecular-weight protein excretion in pediatric idiopathic nephrotic syndrome

Authors
Chehade, Hassib
Werner, Dominique
Mosig, Dolores
Cachat, Francois
Published in Pediatric Nephrology. 2013, vol. 28, no. 12, p. 2299-306
Abstract Minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) are the most common causes of idiopathic nephrotic syndrome (INS). We have evaluated the reliability of urinary neutrophil-gelatinase-associated lipocalin (uNGAL), urinary alpha1-microglobulin (uα1M) and urinary N-acetyl-beta-D-glucosaminidase (uβNAG) as markers for differentiating MCD from FSGS. We have also evaluated whether these proteins are associated to INS relapses or to glomerular filtration rate (GFR).
Identifiers
PMID: 23949592
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Article (Published version) (283 Kb) - document accessible for UNIGE members only Limited access to UNIGE
Structures
Research group Pathogénèse du syndrome néphrotique idiopathique de l'enfant (180)
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CHEHADE, Hassib et al. Urinary low-molecular-weight protein excretion in pediatric idiopathic nephrotic syndrome. In: Pediatric Nephrology, 2013, vol. 28, n° 12, p. 2299-306. https://archive-ouverte.unige.ch/unige:35508

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Deposited on : 2014-04-08

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