Published in Front Pediatr on March 31, 2016
Minimal Change Disease. Clin J Am Soc Nephrol (2016) 0.75
A unified pathogenesis for kidney diseases, including genetic diseases and cancers, by the protein-homeostasis-system hypothesis. Kidney Res Clin Pract (2017) 0.75
Association of Endothelin-1 rs5370 G>T gene polymorphism with the risk of nephrotic syndrome in children. J Nephropathol (2016) 0.75
Nanoscale imaging of clinical specimens using pathology-optimized expansion microscopy. Nat Biotechnol (2017) 0.75
The spectrum of podocytopathies: a unifying view of glomerular diseases. Kidney Int (2007) 5.15
The podocyte's response to injury: role in proteinuria and glomerulosclerosis. Kidney Int (2006) 5.08
Pathologic classification of focal segmental glomerulosclerosis: a working proposal. Am J Kidney Dis (2004) 4.20
Pathology of the nephrotic syndrome in children: a report for the International Study of Kidney Disease in Children. Lancet (1970) 3.78
Podocyte biology and response to injury. J Am Soc Nephrol (2002) 3.25
Nephrotic syndrome in children: prediction of histopathology from clinical and laboratory characteristics at time of diagnosis. A report of the International Study of Kidney Disease in Children. Kidney Int (1978) 2.62
Very low birth weight is a risk factor for secondary focal segmental glomerulosclerosis. Clin J Am Soc Nephrol (2008) 2.57
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. J Am Soc Nephrol (2007) 2.52
Association of histologic variants in FSGS clinical trial with presenting features and outcomes. Clin J Am Soc Nephrol (2012) 2.42
Pathologic classification of focal segmental glomerulosclerosis. Semin Nephrol (2003) 2.27
Current views on collapsing glomerulopathy. J Am Soc Nephrol (2008) 1.96
Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome. Nat Genet (2014) 1.87
Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein. Lancet (1976) 1.82
Congenital nephrotic syndrome of Finnish type. Study of 75 patients. Arch Dis Child (1976) 1.73
C1q nephropathy: a variant of focal segmental glomerulosclerosis. Kidney Int (2003) 1.72
Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients. Kidney Int (2000) 1.65
C1q nephropathy: a distinct pathologic entity usually causing nephrotic syndrome. Am J Kidney Dis (1985) 1.64
The spectrum of focal segmental glomerulosclerosis: new insights. Curr Opin Nephrol Hypertens (2008) 1.61
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Hum Mol Genet (1998) 1.58
Minimal change variants: IgM nephropathy. Clin Nephrol (2006) 1.40
Nephrotic syndrome: pathogenesis and management. Pediatr Rev (2002) 1.19
Pathobiology of focal segmental glomerulosclerosis: new developments. Curr Opin Nephrol Hypertens (2012) 1.14
Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation. Semin Nephrol (2010) 1.13
Genotype-phenotype associations in WT1 glomerulopathy. Kidney Int (2014) 1.10
Immunohistopathologic evaluation of C1q in 800 renal biopsy specimens. Am J Clin Pathol (1985) 1.09
NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum. Hum Mutat (2013) 0.95
Focal segmental glomerulosclerosis: molecular genetics and targeted therapies. BMC Nephrol (2015) 0.90
Graft function 5-7 years after renal transplantation in early childhood. Transplantation (1999) 0.88
Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis. Pediatr Dev Pathol (2008) 0.88
Morphologic variants of focal segmental glomerulosclerosis and their significance. Adv Chronic Kidney Dis (2014) 0.84
Do C1q or IgM nephropathies predict disease severity in children with minimal change nephrotic syndrome? Pediatr Nephrol (2013) 0.82
TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease. Folia Biol (Praha) (2012) 0.81
C1q nephropathy in children: clinical characteristics and outcome. Pediatr Nephrol (2013) 0.81
IgA nephropathy with minimal change disease. Clin J Am Soc Nephrol (2014) 0.79
C1q nephropathy in the pediatric population: pathology and pathogenesis. Pediatr Nephrol (2010) 0.79
Podocyte proteins in congenital and minimal change nephrotic syndrome. Clin Exp Nephrol (2014) 0.77
Novel human pathological mutations. Gene symbol: NPHS1. Disease: congenital nephrotic syndrome, Finnish type. Hum Genet (2009) 0.76
Evolution of hepatic steatosis to fibrosis and adenoma formation in liver-specific growth hormone receptor knockout mice. Front Endocrinol (Lausanne) (2014) 0.81