Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach. - Wikidata - awgldk - TriplyDB

Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach.

Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach.

http://www.wikidata.org/entity/Q36728772

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Long-term Outcomes of Childhood Onset Nephrotic Syndrome Ethnic Differences in Childhood Nephrotic Syndrome Morphology in the Digital Age: Integrating High-Resolution Description of Structural Alterations With Phenotypes and Genotypes Genes Caught In Flagranti: Integrating Renal Transcriptional Profiles With Genotypes and Phenotypes Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era Kidney disease: new technologies translate mechanisms to cure Pro: 'The usefulness of biomarkers in glomerular diseases'. The problem: moving from syndrome to mechanism--individual patient variability in disease presentation, course and response to therapy Patient-Reported Outcomes in Glomerular Disease.suPAR and Team Nephrology Potential urine proteomics biomarkers for primary nephrotic syndrome.Reproducibility of the NEPTUNE descriptor-based scoring system on whole-slide images and histologic and ultrastructural digital images The Rare Diseases Clinical Research Network's organization and approach to observational research and health outcomes research Rare inherited kidney diseases: challenges, opportunities, and perspectives.The primary glomerulonephritides: a systems biology approach.Defining nephrotic syndrome from an integrative genomics perspective.Digital pathology evaluation in the multicenter Nephrotic Syndrome Study Network (NEPTUNE)The grand challenge of nephrology A reassessment of soluble urokinase-type plasminogen activator receptor in glomerular disease Morphometry Predicts Early GFR Change in Primary Proteinuric Glomerulopathies: A Longitudinal Cohort Study Using Generalized Estimating Equations.tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.The Application of Digital Pathology to Improve Accuracy in Glomerular Enumeration in Renal Biopsies.International Network of Chronic Kidney Disease cohort studies (iNET-CKD): a global network of chronic kidney disease cohorts Complete Remission in the Nephrotic Syndrome Study Network.Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.Optimizing Enrollment of Patients into Nephrology Research Studies.Tissue transcriptome-driven identification of epidermal growth factor as a chronic kidney disease biomarker The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network.Techniques and Approaches to Genetic Analyses in Nephrological Disorders.Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.Defining cell-type specificity at the transcriptional level in human disease Novel biomarkers in glomerular disease.The Role of Proprotein Convertase Subtilisin/Kexin Type 9 in Nephrotic Syndrome-Associated Hypercholesterolemia.How can genetics and epigenetics help the nephrologist improve the diagnosis and treatment of chronic kidney disease patients?Design and Methods of the Korean Organ Transplantation Registry.Renal biopsy-driven molecular target identification in glomerular disease.Blood Pressure and Visit-to-Visit Blood Pressure Variability Among Individuals With Primary Proteinuric Glomerulopathies.Hurdles to the introduction of new therapies for immune-mediated kidney diseases.The relatively poor correlation between random and 24-hour urine protein excretion in patients with biopsy-proven glomerular diseases Nephrotic syndrome in infants and children: pathophysiology and management.A comprehensive narrative review of diagnostic biomarkers in human primary membranous nephropathy.

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Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach.

http://www.wikidata.org/entity/Q36728772

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Design of the Nephrotic Syndro ...... a multidisciplinary approach.

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Kidney International

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Design of the Nephrotic Syndro ...... a multidisciplinary approach.

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Akinlolu O Ojo

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Alicia M Neu

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Christine B Sethna

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Chrysta C Lienczewski

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Crystal A Gadegbeku

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Cynthia C Nast

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P2860

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

Distribution of primary renal diseases leading to end-stage renal failure in the United States, Europe, and Australia/New Zealand: results from an international comparative study

Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy

Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond

Sample size planning for developing classifiers using high-dimensional DNA microarray data.

Regularized binormal ROC method in disease classification using microarray data.

Integrative analysis of -omics data and histologic scoring in renal disease and transplantation: renal histogenomics.

Understanding kidney disease: toward the integration of regulatory networks across species.

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10.1038/KI.2012.428

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4

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Stephen M. Hewitt

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Matthew G Sampson

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