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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation.
- Published in:
- Clinical Kidney Journal, 2015, v. 8, n. 5, p. 538, doi. 10.1093/ckj/sfv063
- By:
- Publication type:
- Article
Growth in children with nephrotic syndrome: a post hoc analysis of the NEPTUNE study.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 9, p. 2691, doi. 10.1007/s00467-024-06375-9
- By:
- Publication type:
- Article
Longitudinal analysis of blood pressure and lipids in childhood nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 7, p. 2161, doi. 10.1007/s00467-024-06301-z
- By:
- Publication type:
- Article
A reappraisal of risk factors for hypertension after pediatric acute kidney injury.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 5, p. 1599, doi. 10.1007/s00467-023-06222-3
- By:
- Publication type:
- Article
Patient level factors increase risk of acute kidney disease in hospitalized children with acute kidney injury.
- Published in:
- Pediatric Nephrology, 2023, v. 38, n. 10, p. 3465, doi. 10.1007/s00467-023-05997-9
- By:
- Publication type:
- Article
Hiding in plain sight: genetics of childhood steroid-resistant nephrotic syndrome in Sub-Saharan Africa.
- Published in:
- Pediatric Nephrology, 2023, v. 38, n. 7, p. 2003, doi. 10.1007/s00467-022-05831-8
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- Publication type:
- Article
Treatment of steroid-resistant nephrotic syndrome in the genomic era.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 11, p. 2279, doi. 10.1007/s00467-018-4093-1
- By:
- Publication type:
- Article
Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 8, p. 1435, doi. 10.1007/s00467-019-04237-3
- By:
- Publication type:
- Article
Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 3, p. 539, doi. 10.1007/s00467-018-4103-3
- By:
- Publication type:
- Article
Association of infections and venous thromboembolism in hospitalized children with nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 2, p. 261, doi. 10.1007/s00467-018-4072-6
- By:
- Publication type:
- Article
Genetics of childhood steroid-sensitive nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 9, p. 1481, doi. 10.1007/s00467-016-3456-8
- By:
- Publication type:
- Article
Vesicoureteral reflux and the extracellular matrix connection.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 4, p. 565, doi. 10.1007/s00467-016-3386-5
- By:
- Publication type:
- Article
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.
- Published in:
- Pediatric Nephrology, 2016, v. 31, n. 2, p. 247, doi. 10.1007/s00467-015-3203-6
- By:
- Publication type:
- Article
The impact of disease duration on quality of life in children with nephrotic syndrome: a Midwest Pediatric Nephrology Consortium study.
- Published in:
- Pediatric Nephrology, 2015, v. 30, n. 9, p. 1467, doi. 10.1007/s00467-015-3074-x
- By:
- Publication type:
- Article
Gaining the Patient Reported Outcomes Measurement Information System (PROMIS) perspective in chronic kidney disease: a Midwest Pediatric Nephrology Consortium study.
- Published in:
- Pediatric Nephrology, 2014, v. 29, n. 12, p. 2347, doi. 10.1007/s00467-014-2858-8
- By:
- Publication type:
- Article
Treatment outcome of late steroid-resistant nephrotic syndrome: a study by the Midwest Pediatric Nephrology Consortium.
- Published in:
- Pediatric Nephrology, 2013, v. 28, n. 8, p. 1235, doi. 10.1007/s00467-013-2483-y
- By:
- Publication type:
- Article
Pathogenesis and therapy of focal segmental glomerulosclerosis: an update.
- Published in:
- Pediatric Nephrology, 2011, v. 26, n. 7, p. 1001, doi. 10.1007/s00467-010-1692-x
- By:
- Publication type:
- Article
Significance of hemolysis on extracorporeal life support after cardiac surgery in children.
- Published in:
- Pediatric Nephrology, 2009, v. 24, n. 3, p. 589, doi. 10.1007/s00467-008-1047-z
- By:
- Publication type:
- Article
Exclusion of homozygous PLCE1 ( NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
- Published in:
- Pediatric Nephrology, 2009, v. 24, n. 2, p. 281, doi. 10.1007/s00467-008-1025-5
- By:
- Publication type:
- Article
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 9, p. 1455, doi. 10.1007/s00467-008-0861-7
- By:
- Publication type:
- Article
APOL1 Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K Variant.
- Published in:
- 2024
- By:
- Publication type:
- Letter
FSGS Recurrence Collaboration: Report of a Symposium.
- Published in:
- 2024
- By:
- Publication type:
- Letter
Population Pharmacokinetics of Caffeine in Neonates with Congenital Heart Disease and Associations with Acute Kidney Injury.
- Published in:
- Journal of Clinical Pharmacology, 2024, v. 64, n. 3, p. 300, doi. 10.1002/jcph.2382
- By:
- Publication type:
- Article
Responsiveness of the PROMIS® measures to changes in disease status among pediatric nephrotic syndrome patients: a Midwest pediatric nephrology consortium study.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Gaining the PROMIS perspective from children with nephrotic syndrome: a Midwest pediatric nephrology consortium study.
- Published in:
- Health & Quality of Life Outcomes, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1477-7525-11-30
- By:
- Publication type:
- Article
Gaining the PROMIS perspective from children with nephrotic syndrome: a Midwest pediatric nephrology consortium study.
- Published in:
- 2013
- By:
- Publication type:
- journal article
4531 Setting the Stage for Research Success: Creation of Standardized Physician-Scientist Training Program Guidelines to Facilitate Research During Clinical Training.
- Published in:
- 2020
- By:
- Publication type:
- Abstract
Neutropenic enterocolitis (typhlitis) in a pediatric renal transplant patient. A case report and review of the literature.
- Published in:
- Pediatric Transplantation, 2017, v. 21, n. 6, p. n/a, doi. 10.1111/petr.13022
- By:
- Publication type:
- Article
Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 4, p. 509, doi. 10.1007/s00467-006-0377-y
- By:
- Publication type:
- Article
Role of TGF-β1 in renal parenchymal scarring following childhood urinary tract infection.
- Published in:
- Kidney International, 2002, v. 61, n. 1, p. 61, doi. 10.1046/j.1523-1755.2002.00110.x
- By:
- Publication type:
- Article
National survey found that managing childhood nephrotic syndrome in Nigeria varied widely and did not comply with the best evidence.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Changing epidemiology of nephrotic syndrome in Nigerian children: A cross-sectional study.
- Published in:
- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0239300
- By:
- Publication type:
- Article
A randomized controlled trial of preemptive rituximab to prevent recurrent focal segmental glomerulosclerosis post-kidney transplant (PRI-VENT FSGS): protocol and study design.
- Published in:
- Frontiers in Nephrology, 2023, v. 3, p. 1, doi. 10.3389/fneph.2023.1181076
- By:
- Publication type:
- Article
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.
- Published in:
- Nature Genetics, 2006, v. 38, n. 12, p. 1397, doi. 10.1038/ng1918
- By:
- Publication type:
- Article
The author replies.
- Published in:
- 2015
- By:
- Publication type:
- commentary
The Author Replies:.
- Published in:
- Kidney International, 2015, v. 87, n. 4, p. 859, doi. 10.1038/ki.2015.39
- By:
- Publication type:
- Article
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
- Published in:
- Kidney International, 2014, v. 86, n. 6, p. 1253, doi. 10.1038/ki.2014.305
- By:
- Publication type:
- Article
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
- Published in:
- Kidney International, 2012, v. 81, n. 1, p. 94, doi. 10.1038/ki.2011.297
- By:
- Publication type:
- Article
FO068 The LMX1βR246Q Mutation Induces Podocyte Injury Through Dysregulation of Cholesterol Transport Gene Expression.
- Published in:
- Nephrology Dialysis Transplantation, 2019, v. 34, p. N.PAG, doi. 10.1093/ndt/gfz096.FO068
- By:
- Publication type:
- Article
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 11, p. 3527, doi. 10.1093/ndt/gfn271
- By:
- Publication type:
- Article
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 4, p. 1291
- By:
- Publication type:
- Article
Enuresis in children and adolescents with sickle cell anaemia is more frequent and substantially different from the general population.
- Published in:
- PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201860
- By:
- Publication type:
- Article
Innovations in MD-only physician-scientist training: experiences from the Burroughs Wellcome Fund physician-scientist institutional award initiative.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Addressing the physician-scientist pipeline: strategies to integrate research into clinical training programs.
- Published in:
- 2020
- By:
- Publication type:
- journal article
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Dysregulation of WTI (−KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation.
- Published in:
- Scientific Reports, 2017, p. 39933, doi. 10.1038/srep39933
- By:
- Publication type:
- Article