ReviewPediatric nephrology (Berlin, Germany)2004
Genetic forms of nephrotic syndrome.
Review in Pediatric nephrology (Berlin, Germany), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
21 citing papers in PubMed, 94 citations in OpenAlex.
- Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis.JCI insight · 2022Article
- End-stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygousClinical case reports · 2021Article
- A cross-sectional study exploring disease characteristics and phylogenetic nature of human cytomegalovirus among infected neonates with congenital nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2020Article
- The changing landscape of live kidney donation in the United States from 2005 to 2017.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019Article
- Nephrotic syndrome and mitochondrial disorders: answers.Pediatric nephrology (Berlin, Germany) · 2019Article
- The Role of p.Ser1105Ser (inMedicina (Kaunas, Lithuania) · 2019Article
- Kidney Injury by Variants in theInternational journal of molecular sciences · 2019Article
- Mechanism of cystogenesis in nephrotic kidneys: a histopathological study.BMC nephrology · 2014Article
- Genetic susceptibility to idiopathic membranous nephropathy in high-prevalence Area, Taiwan.BioMedicine · 2014Article
- Physiopathology of idiopathic nephrotic syndrome: lessons from glucocorticoids and epigenetic perspectives.Pediatric nephrology (Berlin, Germany) · 2012Review
- Neonatal nephrotic syndrome associated with placental transmission of proinflammatory cytokines.Pediatric nephrology (Berlin, Germany) · 2011Article
- Recurrence of membranoproliferative glomerulonephritis after renal transplantation in Denys-Drash.Pediatric nephrology (Berlin, Germany) · 2011Article
- Molecular and genetic basis of inherited nephrotic syndrome.International journal of nephrology · 2011Article
- Living donor kidney transplantation in patients with hereditary nephropathies.Nature reviews. Nephrology · 2010Review
- Article
- Congenital nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2009Review
- Low birth weight, but not postnatal weight gain, aggravates the course of nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2007Article
- Predictors of long-term outcome of children with idiopathic focal segmental glomerulosclerosis.Pediatric nephrology (Berlin, Germany) · 2007Article
- Educational feature on focal segmental glomerulosclerosis (FSGS): an introduction.Pediatric nephrology (Berlin, Germany) · 2007Article
- Predictive factors of chronic kidney disease in primary focal segmental glomerulosclerosis.Pediatric nephrology (Berlin, Germany) · 2006Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mutations of NPHS1, NPHS2, or WT1 may be responsible for severe forms of nephrotic syndrome in children, progressing to end-stage renal failure. Recent studies have shown that congenital nephrotic syndrome may be secondary to mutations of one of these three genes and that some patients have a digenic inheritance of NPHS1 and NPHS2 mutations. The clinical spectrum of NPHS2 mutations has broadened, with the demonstration that mutations in the respective gene podocin may be responsible for nephrotic syndrome occurring at birth, in childhood, or in adulthood. It is now well recognized that podocin mutations are found in 10%-30% of sporadic cases of steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis. Data from large cohorts indicate that the risk of recurrence of nephrotic syndrome after renal transplantation in patients with podocin mutations is very low.
Indexed as
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.