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Subject Areas on Research
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A new locus for familial FSGS on chromosome 2p.
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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
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AKI in Children Hospitalized with Nephrotic Syndrome.
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Aberrant IgM on T cells: biomarker or pathogenic factor in childhood nephrotic syndrome?
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Adrenocorticotropic Hormone for Childhood Nephrotic Syndrome: The ATLANTIS Randomized Trial.
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An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome.
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Antecedent renal disease and the outcome of pregnancy.
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Appearance of immune complex glomerulonephritis following the onset of type I diabetes mellitus in a child.
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Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease.
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Association of infections and venous thromboembolism in hospitalized children with nephrotic syndrome.
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COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.
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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
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Case for the panel Nephrotic syndrome with fibrillary and lipid deposits.
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Changing epidemiology of nephrotic syndrome in Nigerian children: A cross-sectional study.
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Collapsing glomerulopathy in 19 patients with systemic lupus erythematosus or lupus-like disease.
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Comparing Presenting Clinical Features in 48 Children With Microscopic Polyangiitis to 183 Children Who Have Granulomatosis With Polyangiitis (Wegener's): An ARChiVe Cohort Study.
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Complete Remission in the Nephrotic Syndrome Study Network.
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De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.
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Deaths in childhood nephrotic syndrome in Ibadan, Nigeria.
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Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach.
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Digital pathology evaluation in the multicenter Nephrotic Syndrome Study Network (NEPTUNE).
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Evolving concepts of the intrarenal renin-angiotensin system in health and disease: contributions of molecular biology.
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Focal segmental glomerulosclerosis associated with nephrotic syndrome in cholesterol atheroembolism: clinicopathological correlations.
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Gaining the PROMIS perspective from children with nephrotic syndrome: a Midwest pediatric nephrology consortium study.
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Genetic Basis of Health Disparity in Childhood Nephrotic Syndrome.
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Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.
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Genetic testing in nephrotic syndrome--challenges and opportunities.
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Genetics of childhood steroid-sensitive nephrotic syndrome.
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Global glomerulosclerosis with nephrotic syndrome; the clinical importance of age adjustment.
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Glomerulopathies with fibrillary deposits.
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HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
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Idiopathic collapsing focal segmental glomerulosclerosis: a clinicopathologic study.
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Inaccuracy of the Schwartz formula in estimating glomerular filtration rate in Nigerian children.
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Increased steroid responsiveness of young children with nephrotic syndrome in Nigeria.
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Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
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Lithium-induced nephrotic syndrome.
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Looking at renal failure upside down.
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Losing their footing: Rac1 signaling causes podocyte detachment and FSGS.
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Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
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Management of childhood onset nephrotic syndrome.
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Management patterns of childhood-onset nephrotic syndrome.
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Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
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Mycotic aneurysm of the thoracoabdominal aorta in a child with end-stage renal disease.
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National survey found that managing childhood nephrotic syndrome in Nigeria varied widely and did not comply with the best evidence.
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Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe disease.
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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
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Open-Label Clinical Trials of Oral Pulse Dexamethasone for Adults with Idiopathic Nephrotic Syndrome.
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Pediatric biopsy of a single native kidney.
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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.
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Potential donor-recipient MYH9 genotype interactions in posttransplant nephrotic syndrome after pediatric kidney transplantation.
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Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings.
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Renin-angiotensin-aldosterone system in nephrotic syndrome.
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Reproducibility and Feasibility of Strategies for Morphologic Assessment of Renal Biopsies Using the Nephrotic Syndrome Study Network Digital Pathology Scoring System.
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Resolution of primary amyloidosis during chemotherapy. Studies in a patient with nephrotic syndrome.
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Responsiveness of the PROMIS® measures to changes in disease status among pediatric nephrotic syndrome patients: a Midwest pediatric nephrology consortium study.
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Role of urine and serum protein electrophoresis in evaluation of nephrotic-range proteinuria.
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Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
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Staphylococcus aureus pneumonia, hyponatremia, hypertension, proteinuria, and hematuria in a 14-year-old boy.
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System for integrated adherence monitoring: real-time non-adherence risk assessment in pediatric kidney transplantation.
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The Application of Digital Pathology to Improve Accuracy in Glomerular Enumeration in Renal Biopsies.
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The impact of disease duration on quality of life in children with nephrotic syndrome: a Midwest Pediatric Nephrology Consortium study.
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The nephrotic syndrome in congenital syphilis: an immunopathy.
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The predominance of membranoproliferative glomerulonephritis in childhood nephrotic syndrome in Ibadan, Nigeria.
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Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
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Translating genetic findings in hereditary nephrotic syndrome: the missing loops.
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Treatment of steroid-resistant nephrotic syndrome in the genomic era.
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Treatment outcome of late steroid-resistant nephrotic syndrome: a study by the Midwest Pediatric Nephrology Consortium.
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Unexpected role of TRPC6 channel in familial nephrotic syndrome: does it have clinical implications?
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Urine and serum lactic dehydrogenase, lactic dehydrogenase isoenzymes, and alkaline phosphatase in the nephrotic syndrome.
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Using PROMIS® to create clinically meaningful profiles of nephrotic syndrome patients.