Disease: Congenital nephrotic syndrome
- 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
- 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
- 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
- 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
- Efficacy and prognosis of infant kidney transplantation
- 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 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
- 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
- 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
- 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
- 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
- Quantitative phenotyping of <em>Nphs1</em> knockout mice as a prerequisite for gene replacement studies
- 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
- Should we integrate the gut microbiota composition to manage idiopathic nephrotic syndrome?
- 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