• A Case of Congenital Nephrotic Syndrome with Crescents Caused by a Novel Compound Heterozygous Pairing of NPHS1 Genetic Variants
• A novel flow cytometry panel to identify prognostic markers for steroid-sensitive forms of idiopathic nephrotic syndrome in childhood
• A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report
• A novel variant in ALG1 gene associated with congenital disorder of glycosylation: A case report and short literature review
• A Rare De Novo Mutation in the TRIM8 Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report
• A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients
• A Unifying Theory for Idiopathic Nephrotic Syndrome Pathogenesis?
• A Yet Unrecognized Cause of Unusually High Levothyroxine Replacement Dose: Protein-Losing Enteropathy
• Access to expensive therapies and diagnostics for kidney care in Switzerland
• Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children
• Arterial Stiffness and Cardiac Functions in Children with Idiopathic Nephrotic Syndrome
• Assessment of Interleukin-15 (IL-15) Concentration in Children with Idiopathic Nephrotic Syndrome
• Case of Pierson syndrome presented with hyphema,vitrous haemorrhage and subsequent neovascular glaucoma
• Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant
• Clinical characteristics of infants hospitalized with early congenital syphilitic nephropathy: a single-center retrospective cross-sectional study in China
• Clinical prediction tool to identify children at risk of pulmonary embolism
• Collapsing Glomerulopathy in a Patient with a TRPC6 Mutation Presenting as Rapidly Progressive Glomerulonephritis: A Case Report and Review of the Literature
• Comprehensive mapping of B lymphocyte immune dysfunction in idiopathic nephrotic syndrome children
• Congenital Nephrotic Syndrome
• Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene
• Congenital Nephrotic Syndrome: Role of Podxl Gene
• Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families
• Correlation between Toll-like Receptor Gene Polymorphisms and Idiopathic Nephrotic Syndrome in Chinese Children
• Corrigendum: Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a NPHS1 Maori founder variant
• Deaths: Leading Causes for 2020
• Delayed diagnosis and exacerbation of hyperlipidemia in idiopathic nephrotic syndrome in children during the COVID-19 pandemic
• Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure
• Effectiveness of Supramaximal Angiotensin-converting Enzyme Inhibition in Controlling Proteinuria in Congenital Nephrotic Syndrome with Cytomegalovirus Infection and an NPHS1 Mutation
• Efficacy and prognosis of infant kidney transplantation
• Expanding the spectrum of LAMB2: Pierson syndrome associated with neuromuscular junction disorder in two patients
• Factors predicting the occurrence of disease-causing variants on next-generation sequencing in children with steroid-resistant nephrotic syndrome - implications for resource-constrained settings
• Feasibility of discontinuing immunosuppression in children with idiopathic nephrotic syndrome
• Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome
• Genetic Causes of Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis
• Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life
• Genetic Studies in Infants with Congenital Nephrotic Syndrome: A Case Series
• Growth Parameters in Adolescents With Idiopathic Nephrotic Syndrome Diagnosed at the Age of 1-6 Years
• Hypercalcemia Secondary to Elevated PTHrP in an Infant Followed by Progression to Nephrotic Syndrome
• Idiopathic nephrotic syndrome in Syrian children: clinicopathological spectrum, treatment, and outcomes
• Immunogenicity, Immunological Memory and Monitoring of Disease Activity Following an Anamnestic Immunization With the 13-Valent Pneumococcal Conjugate Vaccine in Children With Idiopathic Nephrotic Syndrome
• Impact of childhood nephrotic syndrome on obesity and growth: a prospective cohort study
• Inborn Errors of Immunity in Children With Invasive Pneumococcal Disease: A Multicenter Prospective Study
• Insight into prevalence, etiology, and modalities of pediatric chronic dialysis: a comprehensive nationwide analysis
• Intussusception as a complication of idiopathic nephrotic syndrome
• Is kidney biopsy necessary in children with idiopathic nephrotic syndrome?
• LAMB2 gene: broad clinical spectrum in Pierson syndrome
• Late nephrectomy in infants with congenital nephrotic syndrome of the Finnish type
• Less or later: Treatment dilemmas in congenital nephrotic syndrome
• Machine learning models for predicting steroid-resistant of nephrotic syndrome
• Managing venous thrombosis in a pediatric patient with short bowel and congenital nephrotic syndromes: a case report emphasizing rivaroxaban level monitoring
• Membranoproliferative glomerulonephritis in a child with congenital portosystemic shunt
• Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre Study
• More than four decades of graft survival in pediatric kidney transplant recipients
• Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children
• Neonatal nephrotic syndrome: all is not gloomy
• Nephrotic Syndrome
• Nephrotic Syndrome Throughout Childhood: Diagnosing Podocytopathies From the Womb to the Dorm
• Neurocognitive Profile in Pediatric Kidney Transplant Candidates: Effects of Medical and Sociodemographic Factors
• New insights from the genetic work-up in early onset nephrotic syndrome: report from a registry in western India
• Novel sphingosine-1-phosphate lyase mutation causes multisystemic diseases: case report
• Nutritional Management of Idiopathic Nephrotic Syndrome in Pediatric Age
• Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis
• Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome
• Phenotypic quantification of Nphs1-deficient mice
• Polymerizing laminins in development, health, and disease
• Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
• Quantitative phenotyping of <em>Nphs1</em> knockout mice as a prerequisite for gene replacement studies
• Regular prophylaxis with activated prothrombin complex concentrates in pediatric hemophilia
• Repeated implants failure in young patient with idiopathic nephrotic syndrome: a case report with brief review of the literature
• Risk Factors for Relapse in Childhood Nephrotic Syndrome
• Rituximab in idiopathic nephrotic syndrome: still waiting for stronger evidences
• Rituximab-associated hypogammaglobulinemia in children with idiopathic nephrotic syndrome: results of an ESPN survey
• SARS-CoV-2 Infection in Children with Idiopathic Nephrotic Syndrome: A Multicentric Study
• Serological responses to immunization during nephrosis in infants with congenital nephrotic syndrome of the Finnish type
• Should we integrate the gut microbiota composition to manage idiopathic nephrotic syndrome?
• Splenic Dysfunction in Children With Sickle Cell Disease: A Single Centre Experience From Central India
• Steroid induced ocular complications in idiopathic nephrotic syndrome: a cross sectional single center study
• Successful global anti-B-cell strategy with daratumumab in a patient with post-transplant nephrotic syndrome recurrence unresponsive to immunoadsorption and obinutuzumab
• Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in <em>LAMB2</em>-Associated Disease
• Three Novel Heterozygous Mutations of NPHS1 Gene Causing Infants with Congenital Nephrotic Syndrome: Two Chinese (Han) Cases
• Tumor necrosis factor alpha gene polymorphism affects the pattern of idiopathic nephrotic syndrome in Kuwaiti Arab children
• Urinary Apolipoprotein A1 and Neutrophil Gelatinase-associated Lipocalin in Children with Idiopathic Nephrotic Syndrome
• Usefulness of Early Genetic Diagnosis for Twins With a Family History of Congenital Nephrotic Syndrome