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Journal of the Formosan Medical Association, ISSN 0929-6646, 2017, Volume 117, Issue 1, pp. 48 - 53
Abstract Background/Purpose Nephrotic syndrome is the commonest etiology of proteinuria in children. Steroid-resistant nephrotic syndrome (SRNS) is defined by... 
Internal Medicine | Egyptian children | NPHS2 | steroid-resistant nephrotic syndrome | MEDICINE, GENERAL & INTERNAL | WT1 | NPHS2 MUTATIONS | PODOCIN | PREVALENCE | SPECTRUM | FOCAL SEGMENTAL GLOMERULOSCLEROSIS
Journal Article
IRANIAN JOURNAL OF KIDNEY DISEASES, ISSN 1735-8582, 05/2019, Volume 13, Issue 3, pp. 165 - 172
Introduction. Nephrotic syndrome is a heterogeneous disease in children, with nearly 10% categorized as steroid-resistant. In this study we evaluated disease... 
SRNS | NPHS2 GENE | WES | NEPHRIN | PREVALENCE | CHILDHOOD | nephrotic syndrome | CHILDREN | NPHS1 | NPHS2 | WT1 | FAT1 | UROLOGY & NEPHROLOGY | PODOCIN | COHORT | SPECTRUM | FOCAL SEGMENTAL GLOMERULOSCLEROSIS
Journal Article
AMERICAN JOURNAL OF KIDNEY DISEASES, ISSN 0272-6386, 11/2018, Volume 72, Issue 5, pp. S22 - S25
Nephrotic syndrome is the most common glomerular disease in children. There is wide variation in the incidence of nephrotic syndrome in different populations,... 
KIDNEY-DISEASE | RISK LOCI | AFRICAN-AMERICAN CHILDREN | FSGS | UROLOGY & NEPHROLOGY | NPHS2 MUTATIONS | APOL1 VARIANTS | PATTERNS | NEPHROTIC SYNDROME | HLA-DQA1
Journal Article
by Wang, Y and Dang, XQ and He, QN and Zhen, Y and He, XX and Yi, ZW and Zhu, KC
GENE, ISSN 0378-1119, 08/2017, Volume 625, pp. 15 - 20
Approximately 20% of children with idiopathic nephrotic syndrome do not respond to steroid therapy. More than 30 genes have been identified as disease-causing... 
GENE-MUTATIONS | SRNS | Steroid-resistant | VARIANTS | Gene mutation | NPHS2 | WT1 | GUIDELINES | GENETICS & HEREDITY | Nephrotic syndrome | NGS
Journal Article
03/2012
Glomerular podocytes are highly specialized cells with a complex cytoarchitecture. Their most prominent features are interdigitated foot processes with... 
primary nephrotic syndrome | NPHS2 mutations | podocyte
Web Resource
Journal of Shanghai Jiaotong University (Medical Science), ISSN 1674-8115, 11/2017, Volume 37, Issue 11, pp. 1476 - 1481
Journal Article
by Li, YZ and He, QN and Wang, Y and Dang, XQ and Wu, XC and Li, XY and Shuai, LJ and Yi, ZW
ANNALS OF CLINICAL AND LABORATORY SCIENCE, ISSN 0091-7370, 05/2019, Volume 49, Issue 3, pp. 330 - 337
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 05/2011, Volume 121, Issue 5, pp. 2013 - 2024
Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of end-stage renal failure. Identification of single-gene causes of SRNS has generated some... 
MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | GENE | COENZYME-Q BIOSYNTHESIS | DIPHOSPHATE SYNTHASE SUBUNIT-2 | NPHS2 | GLOMERULAR PROTEIN | UBIQUINONE BIOSYNTHESIS | COQ DEFICIENCY | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | SACCHAROMYCES-CEREVISIAE | Deafness | Gene mutations | Genetic aspects | Nephrotic syndrome | Research | Health aspects | Risk factors
Journal Article
PLOS ONE, ISSN 1932-6203, 10/2017, Volume 12, Issue 10
Mutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early disease... 
SEGMENTAL GLOMERULOSCLEROSIS | PIERSON-SYNDROME | MULTIDISCIPLINARY SCIENCES | MUTANT PODOCIN | ELECTRON-MICROSCOPY | NPHS2 MUTATIONS | DIABETIC-NEPHROPATHY | ALPORT-SYNDROME | SEVERE RENAL-DISEASE | UP-REGULATION | LAMININ BETA-2
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 04/2017, Volume 91, Issue 4, pp. 937 - 947
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 05/2017, Volume 28, Issue 5, pp. 1614 - 1621
Journal Article
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 2015, Volume 10, Issue 4, pp. 592 - 600
Background and objectives Steroid-resistant nephrotic syndrome is a rare kidney disease involving either immune-mediated or genetic alterations of podocyte... 
UROLOGY & NEPHROLOGY | PATTERNS | THERAPY | MUTATIONS | CYCLOPHOSPHAMIDE | NPHS2 | Recurrence | Age Distribution | Prospective Studies | Glomerulosclerosis, Focal Segmental - genetics | Humans | Immunosuppressive Agents - therapeutic use | Nephrosis, Lipoid - epidemiology | Child, Preschool | Infant | Male | Nephrotic Syndrome - genetics | Nephrotic Syndrome - congenital | Young Adult | DNA Mutational Analysis | Female | Registries | Nephrotic Syndrome - therapy | Retrospective Studies | Child | Nephrotic Syndrome - diagnosis | Infant, Newborn | Latin America - epidemiology | Genetic Predisposition to Disease | Nephrosis, Lipoid - diagnosis | Glomerulosclerosis, Focal Segmental - epidemiology | Risk Factors | Europe - epidemiology | Treatment Outcome | Kidney Transplantation | Nephrosis, Lipoid - therapy | Genetic Markers | Nephrosis, Lipoid - genetics | Glomerulonephritis, Membranoproliferative - therapy | Remission Induction | Glomerulosclerosis, Focal Segmental - diagnosis | Glomerulonephritis, Membranoproliferative - genetics | Middle East - epidemiology | Phenotype | Biopsy | Adolescent | Age of Onset | Nephrotic Syndrome - epidemiology | Glomerulonephritis, Membranoproliferative - diagnosis | Glomerulosclerosis, Focal Segmental - therapy | Mutation | Glomerulonephritis, Membranoproliferative - epidemiology | podocytopathies | nephrin | children | WT1 | Original | podocin
Journal Article