[HTML][HTML] Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier

M Zenker, E Machuca, C Antignac - Journal of Molecular Medicine, 2009 - Springer
Nephrotic syndrome is caused by increased permeability of the glomerular filtration barrier
for macromolecules. The identification of mutations of various podocyte-expressed proteins …

[HTML][HTML] Plasma soluble urokinase receptor levels are increased but do not distinguish primary from secondary focal segmental glomerulosclerosis

J Huang, G Liu, YM Zhang, Z Cui, F Wang, XJ Liu… - Kidney international, 2013 - Elsevier
In this study, we measured soluble urokinase receptor levels, a possible permeability factor,
in the plasma of patients with primary focal segmental glomerulosclerosis (FSGS) and …

[引用][C] Inherited nephroses

A Weins, MR Pollak - Molecular and Genetic Basis of Renal Disease, 2008 - Elsevier

Recurrence of nephrotic proteinuria in children with focal segmental glomerulosclerosis after renal transplantation treated with plasmapheresis and immunoadsorption

F Fencl, E Simková, K Vondrák, J Janda… - Transplantation …, 2007 - Elsevier
Idiopathic focal segmental glomerulosclerosis (FSGS) is believed to be caused by a
circulating permeability factor. FSGS recurrence is common after transplantation. The …

Does vascular endothelial growth factor (VEGF) play a role in the pathogenesis of minimal change disease?

G Boner, AJ Cox, DJ Kelly, A Tobar… - Nephrology Dialysis …, 2003 - academic.oup.com
Background. Minimal change disease (MCD) is one of the major causes of nephrotic
syndrome both in children and adults. The pathogenesis of this condition is not clear and it …

Sera from patients with collapsing focal segmental glomerulosclerosis increase albumin permeability of isolated glomeruli

ET McCarthy, M Sharma, R Sharma, RJ Falk… - Journal of Laboratory …, 2004 - Elsevier
The collapsing variant of focal segment glomerulosclerosis (FSGS) is characterized by
heavy proteinuria and rapid progression to renal failure. Its cause is not known. We have …

Nephrotic syndrome: molecular and genetic basis

A Fogo - Nephron, 2000 - karger.com
Nephrotic syndrome results from varying injuries to the capillary wall of the glomerulus. The
components of the capillary wall, including the endothelial cell, glomerular basement …

[HTML][HTML] Serum-soluble urokinase receptor levels do not distinguish focal segmental glomerulosclerosis from other causes of nephrotic syndrome in children

A Sinha, J Bajpai, S Saini, D Bhatia, A Gupta… - Kidney International, 2014 - Elsevier
In this prospective study, we measured serum levels of the soluble urokinase receptor
(suPAR) in pediatric patients with nephrotic syndrome of various etiologies. Mean levels of …

[HTML][HTML] Monogenic causes of proteinuria in children

O Cil, F Perwad - Frontiers in medicine, 2018 - frontiersin.org
Glomerular disease is a common cause for proteinuria and chronic kidney disease leading
to end-stage renal disease requiring dialysis or kidney transplantation in children. Nephrotic …

[PDF][PDF] Focal segmental glomerulosclerosis: genetics, mechanism, and therapies

A Kronbichler, J Oh, B Meijers… - BioMed research …, 2016 - lirias.kuleuven.be
Focal segmental glomerulosclerosis (FSGS) is one of the primary glomerular disorders in
both children and adults which can progress to end-stage renal failure. Recent advances in …