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Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Kidney international, 2012-08, Vol.82 (4), p.454-464

2012

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Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

Journal of medical genetics, 2007-03, Vol.44 (3), p.193-199

2007

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Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (5), p.862-864

2015

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C3 Glomerulonephritis Associated With Monoclonal Gammopathy: A Case Series

American journal of kidney diseases, 2013-09, Vol.62 (3), p.506-514

2013

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C3 Glomerulopathy: Ten Years' Experience at Mayo Clinic

Mayo Clinic proceedings, 2018-08, Vol.93 (8), p.991-1008

2018

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Factor H Autoantibodies and Complement-Mediated Diseases

Frontiers in immunology, 2020-12, Vol.11, p.607211-607211

2020

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Serum properdin consumption as a biomarker of C5 convertase dysregulation in C3 glomerulopathy

Clinical and experimental immunology, 2016-04, Vol.184 (1), p.118-125

2016

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WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease

Human mutation, 2015-11, Vol.36 (11), p.1021-1028

2015

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Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort

Clinical journal of the American Society of Nephrology, 2015-04, Vol.10 (4), p.592-600

2015

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PLA2R antibodies, glomerular PLA2R deposits and variations in PLA2R1 and HLA-DQA1 genes in primary membranous nephropathy in South Asians

Nephrology, dialysis, transplantation, 2016-09, Vol.31 (9), p.1486-1493

2016

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C5 nephritic factors drive the biological phenotype of C3 glomerulopathies

Kidney international, 2017-11, Vol.92 (5), p.1232-1241

2017

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Genotype–phenotype analysis of pediatric patients with WT1 glomerulopathy

Pediatric nephrology (Berlin, West), 2017, Vol.32 (1), p.81-89

2017

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A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy

Kidney international, 2017-10, Vol.92 (4), p.876-887

2017

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AJKD Atlas of Renal Pathology: Glomerulonephritis With Dominant C3

American journal of kidney diseases, 2015-10, Vol.66 (4), p.e25-e26

2015

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Novel IL2RB gene defect associated with severe eczema, recurrent infections, lymphoproliferation, and IgA nephropathy

Pediatric allergy and immunology, 2024-06, Vol.35 (6), p.e14160-n/a

2024

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CNDP1 genotype and renal survival in pediatric nephropathies

Journal of pediatric endocrinology & metabolism : JPEM, 2016-07, Vol.29 (7), p.827

2016

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Acute Presentation and Persistent Glomerulonephritis Following Streptococcal Infection in a Patient With Heterozygous Complement Factor H–Related Protein 5 Deficiency

American journal of kidney diseases, 2012-07, Vol.60 (1), p.121-125

2012

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Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

Blood, 2009-11, Vol.114 (19), p.4261-4271

2009

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Clinicopathological features of C3 glomerulopathy in children: a single-center experience

Pediatric nephrology (Berlin, West), 2020, Vol.35 (1), p.153-162

2020

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Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese

Journal of the American Society of Nephrology, 2016-10, Vol.27 (10), p.3187-3194

2016

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Long noncoding RNA FGD5-AS1 alleviates childhood IgA nephropathy by targeting PTEN-mediated JNK/c-Jun signaling pathway via miR-196b-5p

Experimental cell research, 2023-03, Vol.424 (1), p.113481-113481, Article 113481

2023

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C1q nephropathy among children with nephrotic syndrome: Ten-year experience from a pediatric nephrology unit

Turkish journal of pediatrics, 2018-01, Vol.60 (1), p.14-21

2018

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Apoptosis inhibitor of macrophage as a biomarker for disease activity in Japanese children with IgA nephropathy and Henoch-Schönlein purpura nephritis

Pediatric research, 2021-02, Vol.89 (3), p.667-672

2021

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Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits

Pediatric nephrology (Berlin, West), 2016-09, Vol.31 (9), p.1459-1467

2016

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Relationship between genotypes and clinical manifestation, pathology, and cccDNA in Chinese children with hepatitis B virus-associated glomerulonephritis

World journal of pediatrics : WJP, 2016-08, Vol.12 (3), p.347-352

2016

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Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B

C3 Glomerulonephritis Associated With Monoclonal Gammopathy: A Case Series

C3 Glomerulopathy: Ten Years' Experience at Mayo Clinic

Factor H Autoantibodies and Complement-Mediated Diseases

Serum properdin consumption as a biomarker of C5 convertase dysregulation in C3 glomerulopathy

WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort

PLA2R antibodies, glomerular PLA2R deposits and variations in PLA2R1 and HLA-DQA1 genes in primary membranous nephropathy in South Asians

C5 nephritic factors drive the biological phenotype of C3 glomerulopathies

Genotype–phenotype analysis of pediatric patients with WT1 glomerulopathy

A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy

AJKD Atlas of Renal Pathology: Glomerulonephritis With Dominant C3

Novel IL2RB gene defect associated with severe eczema, recurrent infections, lymphoproliferation, and IgA nephropathy

CNDP1 genotype and renal survival in pediatric nephropathies

Acute Presentation and Persistent Glomerulonephritis Following Streptococcal Infection in a Patient With Heterozygous Complement Factor H–Related Protein 5 Deficiency

Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

Clinicopathological features of C3 glomerulopathy in children: a single-center experience

Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese

Long noncoding RNA FGD5-AS1 alleviates childhood IgA nephropathy by targeting PTEN-mediated JNK/c-Jun signaling pathway via miR-196b-5p

C1q nephropathy among children with nephrotic syndrome: Ten-year experience from a pediatric nephrology unit

Apoptosis inhibitor of macrophage as a biomarker for disease activity in Japanese children with IgA nephropathy and Henoch-Schönlein purpura nephritis

Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits

Relationship between genotypes and clinical manifestation, pathology, and cccDNA in Chinese children with hepatitis B virus-associated glomerulonephritis

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