Research & Literature
Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.
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Bambino Gesù Children's Hospital
Rome, Italy
All India Institute of Medical Sciences
New Delhi, India
Hôpital Necker-Enfants Malades
Paris, France
Istituto Giannina Gaslini
Genoa, Italy
Heidelberg University
Heidelberg, Germany
Universität Hamburg
Hamburg, Germany
Hacettepe University
Ankara, Türkiye
University of Michigan
Ann Arbor, United States
Boston Children's Hospital
Boston, United States
Bristol Royal Hospital for Children
Bristol, United Kingdom
References
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Pediatric nephrology (Berlin, Germany) 2022; (37(3)):585-592 doi:10.1007/s00467-021-05211-8.
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Therapeutic Response and Long-Term Renal Outcomes in Childhood Idiopathic Steroid-Resistant Nephrotic Syndrome: A Single-Center Study.
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Risk of Arterial Thromboembolism, Venous Thromboembolism, and Bleeding in Patients with Nephrotic Syndrome: A Population-Based Cohort Study.
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Rituximab Use for the Treatment of Childhood Nephrotic Syndrome by Canadian Pediatric Nephrologists: A National Survey.
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Canadian journal of kidney health and disease 2022; (9()):20543581221079959 doi:10.1177/20543581221079959.
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Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children.
Starcea IM, Bogos RA, Scurtu G, et al.
International journal of general medicine 2022; (15()):4187-4193 doi:10.2147/IJGM.S348346.
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Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, et al.
Kidney international 2022; (102(3)):592-603 doi:10.1016/j.kint.2022.02.040.
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A critical role of the podocyte cytoskeleton in the pathogenesis of glomerular proteinuria and autoimmune podocytopathies.
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Acta physiologica (Oxford, England) 2022; (235(4)):e13850 doi:10.1111/apha.13850.
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Perceived family impact and coping mechanisms of caregivers of children with nephrotic syndrome.
Cocorpus J, Jun J, Basalely A, et al.
Pediatric nephrology (Berlin, Germany) 2023; (38(4)):1177-1185 doi:10.1007/s00467-022-05619-w.
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Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center.
Agrwal S, Mantan M, Dabas A, Batra VV
Indian journal of nephrology 2022; (32(4)):320-326 doi:10.4103/ijn.ijn_258_21.
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Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome.
Jiao J, Wang L, Ni F, et al.
Genes & diseases 2022; (9(6)):1662-1673 doi:10.1016/j.gendis.2022.03.023.
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Streptococcus pneumoniae meningitis in a child with idiopathic nephrotic syndrome: a case report.
Guernsey D, Arun A, Agha R, Kupferman JC
Journal of medical case reports 2022; (16(1)):403 doi:10.1186/s13256-022-03648-5.
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Multiple Venous and Pulmonary Artery Thrombosis as the Presenting Features of Spontaneously Reversible Nephrotic Syndrome after Exposure to SARS-CoV-2 Virus (Pfizer/BioNTech BNT162b2) Vaccination.
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Vaccines 2022; (10(11)) doi:10.3390/vaccines10111888.
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A Systematic Review and Meta-Analysis of the Rate and Risk Factors for Post-transplant Disease Recurrence in Children With Steroid Resistant Nephrotic Syndrome.
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Kidney international reports 2023; (8(2)):254-264 doi:10.1016/j.ekir.2022.10.030.
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Key pathological features characterize minimal change disease-like IgA nephropathy.
Wang TY, Chang FP, Yang AH, et al.
PloS one 2023; (18(7)):e0288384 doi:10.1371/journal.pone.0288384.
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Childhood nephrotic syndrome.
Vivarelli M, Gibson K, Sinha A, Boyer O
Lancet (London, England) 2023; (402(10404)):809-824 doi:10.1016/S0140-6736(23)01051-6.
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Cerebral sinovenous thrombosis in children with nephrotic syndrome: systematic review and one new case.
Konopásek P, Piteková B, Krejčová V, Zieg J
Frontiers in pediatrics 2023; (11()):1207871 doi:10.3389/fped.2023.1207871.
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Diagnostic value of serum CRP, PCT and IL-6 in children with nephrotic syndrome complicated by infection: a single center retrospective study.
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Pediatric research 2024; (95(3)):722-728 doi:10.1038/s41390-023-02830-9.
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Current approaches to overcome recurrent focal segmental glomerulosclerosis after kidney transplantation.
Ahmad SB, Peleg Y, Ahn W
Current opinion in nephrology and hypertension 2024; (33(1)):61-66 doi:10.1097/MNH.0000000000000946.
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Intravenous cyclophosphamide therapy in children with calcineurin inhibitor-resistant steroid-resistant nephrotic syndrome in a resource-limited setting.
Saiteja P, Deepthi B, Krishnasamy S, et al.
Pediatric nephrology (Berlin, Germany) 2024; (39(4)):1149-1160 doi:10.1007/s00467-023-06187-3.
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Drug-induced glomerular diseases.
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Therapie 2024; (79(2)):271-281 doi:10.1016/j.therap.2023.10.010.
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Efficacy of combined rituximab and daratumumab treatment in posttransplant recurrent focal segmental glomerulosclerosis.
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American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2024; (24(4)):688-692 doi:10.1016/j.ajt.2023.12.010.
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Cyclophosphamide Toxicity in Pediatric Nephrotic Syndrome Patient: A Case Report and Literature Review.
Patil S, Patil MV, Bagalkotkar A, Wali S
Current drug safety 2024; (19(4)):489-496 doi:10.2174/0115748863281214231213075642.
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Nephrotic Syndrome in a Child With NPHS2 Mutation.
Tollaksen R, Craver RD, Yosypiv IV
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2024; (27(4)):359-363 doi:10.1177/10935266231223274.
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Risk factors and renal outcomes of AKI in children with secondary steroid-resistant nephrotic syndrome.
Yu N, Ouyang X, Li J, et al.
Renal failure 2024; (46(1)):2314637 doi:10.1080/0886022X.2024.2314637.
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Comparison of different genetic testing modalities applied in paediatric patients with steroid-resistant nephrotic syndrome.
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Italian journal of pediatrics 2024; (50(1)):85 doi:10.1186/s13052-024-01655-4.
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A Review of Focal Segmental Glomerulosclerosis Classification With a Focus on Genetic Associations.
Bonilla M, Efe O, Selvaskandan H, et al.
Kidney medicine 2024; (6(6)):100826 doi:10.1016/j.xkme.2024.100826.
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Autoantibodies Targeting Nephrin in Podocytopathies.
Hengel FE, Dehde S, Lassé M, et al.
The New England journal of medicine 2024; (391(5)):422-433 doi:10.1056/NEJMoa2314471.
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IPNA consensus definitions for clinical trial outcomes in steroid-resistant nephrotic syndrome.
Hari P, Khandelwal P, Boyer O, et al.
Pediatric nephrology (Berlin, Germany) 2025; (40(3)):865-872 doi:10.1007/s00467-024-06543-x.
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An international, multi-center study evaluated rituximab therapy in childhood steroid-resistant nephrotic syndrome.
Chan EY, Sinha A, Yu ELM, et al.
Kidney international 2024; (106(6)):1146-1157 doi:10.1016/j.kint.2024.09.011.
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Management and long-term outcome of recurrent idiopathic FSGS in pediatric kidney transplant recipients.
Plonsky-Toder M, Pollack S, Tibi R, et al.
Scientific reports 2024; (14(1)):25493 doi:10.1038/s41598-024-74184-z.
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Incidence and Risk Factors for Hypertension among Children with Nephrotic Syndrome.
Robinson C, Wagner S, Aman N, et al.
The Journal of pediatrics 2025; (284()):114443 doi:10.1016/j.jpeds.2024.114443.
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Outcomes and prognostic factors in childhood-onset steroid-resistant nephrotic syndrome: a retrospective single-center study.
Zerkowitz E, Gellermann J, Beckus J, et al.
Pediatric nephrology (Berlin, Germany) 2025; (40(7)):2239-2252 doi:10.1007/s00467-025-06705-5.
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Interventions for idiopathic steroid-resistant nephrotic syndrome in children.
Liu ID, Willis NS, Craig JC, Hodson EM
The Cochrane database of systematic reviews 2025; (5()):CD003594 doi:10.1002/14651858.CD003594.pub7.
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Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndrome.
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Human genetics 2025; (144(7)):727-740 doi:10.1007/s00439-025-02752-y.
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Success of Coenzyme Q10 in Treating Steroid-Resistant Nephrotic Syndrome in Jordan: A Case Series.
Frehat MQ, Alhadidi A, Almhairat A, et al.
Cureus 2025; (17(4)):e83231 doi:10.7759/cureus.83231.
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Structural and functional insights of the podocyte slit diaphragm complex.
Qadri AH, Prajapati J, Praghna D, et al.
Tissue barriers 2026; (14(2)):2575198 doi:10.1080/21688370.2025.2575198.
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Lupus podocytopathy as a first renal manifestation in long-standing systemic lupus erythematosus: a case report.
Togashi T, Fujisawa Y, Yano Y, et al.
Modern rheumatology case reports 2025; (9(2)) doi:10.1093/mrcr/rxaf072.
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Managing concurrent nephrotic syndrome, spontaneous bacterial peritonitis, and herpes zoster in an immunocompromised child: Diagnostic difficulties and treatment outcomes.
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IDCases 2026; (43()):e02489 doi:10.1016/j.idcr.2026.e02489.
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KDOQI US Commentary on the KDIGO 2025 Clinical Practice Guideline for the Management of Nephrotic Syndrome in Children.
Wang CS, Gbadegesin R
American journal of kidney diseases : the official journal of the National Kidney Foundation 2026; (87(2)):141-152 doi:10.1053/j.ajkd.2025.10.006.
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Indian journal of pediatrics 2026; (93(5)):507-514 doi:10.1007/s12098-026-06132-w.
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Monogenic variants drive low recurrence risk in pediatric steroid-resistant nephrotic syndrome after kidney transplantation: a high-consanguinity cohort.
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Cutaneous Staphylococcus aureus Infections in Renal Edema Across Kidney Disease and the Intensive Care Unit: Pathophysiological Mechanisms, Clinical Implications, and Therapeutic Challenges.
Caragea ME, Caragea DC, Novac MB, et al.
International journal of molecular sciences 2026; (27(13)) doi:10.3390/ijms27136038.
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