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Clinical usefulness of the Oxford classification in determining immunosuppressive treatment in IgA nephropathy

Annals of medicine (Helsinki), 2017-04, Vol.49 (3), p.217-229

2017

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The Spectrum of Adult Postinfectious Glomerulonephritis in the New Millennium

Renal failure, , Vol.31 (8), p.676-682

Wen, Yao-Ko

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Validation of the 2010 histopathological classification of ANCA-associated glomerulonephritis in a Japanese single-center cohort

Modern rheumatology, 2013-04

2013

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Fibrillary and Immunotactoid Glomerulopathies

Renal failure, 1998-01, Vol.20 (6), p.801-808

1998

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Immunotactoid Glomerulopathy (ITGP): A Not Fully Defined Clinicopathologic Entity

Renal failure, 1993, Vol.15 (3), p.401-405

1993

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Autoimmunity in Nephritis

Autoimmunity, 1990, Vol.6 (4), p.319-328

Ballardie, Francis W.

1990

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Clinical Features and Prognosis in Childhood IgA Nephropathy

Renal failure, 1994, Vol.16 (5), p.629-636

1994

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Development of Renal Failure in IgA Nephropathy: The Importance of Interstitial Infiltration and Deposition of Fibrinogen

Renal failure, 1994, Vol.16 (4), p.511-523

1994

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Experimental Circulating Immune Complex Glomerulonephritis

Renal failure, 1984, Vol.8 (3-4), p.183-187

1984

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Clinical and pathological analysis of IgA nephropathy with chronic renal failure

Renal failure, 2016-10, Vol.38 (9), p.1347-1352

2016

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Renal and overall outcomes of double-positive (ANCA and anti-GBM antibodies) patients compared to ANCA-associated vasculitis patients with severe renal involvement: A multicenter retrospective study with systematic renal pathology analysis

Scandinavian journal of rheumatology, 2022-05, Vol.51 (3), p.205-213

2022

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Clinical and pathologic characteristics of pauci-immune anti-myeloperoxidase antibody associated glomerulonephritis with nephrotic range proteinuria

Renal failure, 2018-11, Vol.40 (1), p.554-560

2018

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Patient Outcomes of Henoch-Schönlein Purpura Nephritis According to the New Semiquantitative Classification

Fetal and pediatric pathology, 2020-09, Vol.39 (5), p.381-389

2020

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Characteristics of patients with coexisting IgA nephropathy and membranous nephropathy

Renal failure, 2018-10, Vol.40 (1), p.213-218

2018

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Unknown aspect of the old disease: does dyslipidemia in systemic AA amyloidosis differ from the dyslipidemia in primary glomerulonephritis?

Renal failure, 2015-09, Vol.37 (8), p.1273-1279

2015

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The role of mammalian target of rapamycin pathway in the pathogenesis of pauci-immune glomerulonephritis

Renal failure, 2019-01, Vol.41 (1), p.907-913

2019

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Clinical and histopathologic profile of patients with primary IgA nephropathy seen in a tertiary hospital in India

Renal failure, 2016-03, Vol.38 (3), p.431-436

2016

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Lupus glomerulonephritis in 788 Chinese children: a multi-centre clinical and histopathological analysis based on 549 renal biopsies

Paediatrics and international child health, 2017-10, Vol.37 (4), p.286-291

2017

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Recent advances in IgG4-related kidney disease

Modern rheumatology, 2023-03, Vol.33 (2), p.242-251

2023

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Monoclonal immunoglobulin-associated proliferative glomerulonephritis characterized by organized deposits of striated ultra-substructures: A case report

Ultrastructural pathology, 2017-07, Vol.41 (4), p.301-307

2017

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Diffuse membranoproliferative glomerulonephritis with focal sclerosis and renal amyloidosis in an adult male with autosomal dominant dystrophic epidermolysis bullosa: a case report

Renal failure, 2019-01, Vol.41 (1), p.850-854

2019

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Familial risks of glomerulonephritis - a nationwide family study in Sweden

Annals of medicine (Helsinki), 2016-07, Vol.48 (5), p.313-322

2016

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Circulating immune-complexes and complement activation through the classical pathway in myeloperoxidase-ANCA-associated glomerulonephritis

Renal failure, 2022-12, Vol.44 (1), p.714-723

2022

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Outcomes of normotensive IgA nephropathy patients with mild proteinuria who have impaired renal function

Renal failure, 2019-01, Vol.41 (1), p.875-882

2019

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Efficacy of antisense monocyte chemoattractant protein-1 (MCP-1) in a rat model of mesangial proliferative glomerulonephritis

Renal failure, 2013-11, Vol.35 (10), p.1418-1428

2013

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Clinical usefulness of the Oxford classification in determining immunosuppressive treatment in IgA nephropathy

The Spectrum of Adult Postinfectious Glomerulonephritis in the New Millennium

Validation of the 2010 histopathological classification of ANCA-associated glomerulonephritis in a Japanese single-center cohort

Fibrillary and Immunotactoid Glomerulopathies

Immunotactoid Glomerulopathy (ITGP): A Not Fully Defined Clinicopathologic Entity

Autoimmunity in Nephritis

Clinical Features and Prognosis in Childhood IgA Nephropathy

Development of Renal Failure in IgA Nephropathy: The Importance of Interstitial Infiltration and Deposition of Fibrinogen

Experimental Circulating Immune Complex Glomerulonephritis

Clinical and pathological analysis of IgA nephropathy with chronic renal failure

Renal and overall outcomes of double-positive (ANCA and anti-GBM antibodies) patients compared to ANCA-associated vasculitis patients with severe renal involvement: A multicenter retrospective study with systematic renal pathology analysis

Clinical and pathologic characteristics of pauci-immune anti-myeloperoxidase antibody associated glomerulonephritis with nephrotic range proteinuria

Patient Outcomes of Henoch-Schönlein Purpura Nephritis According to the New Semiquantitative Classification

Characteristics of patients with coexisting IgA nephropathy and membranous nephropathy

Unknown aspect of the old disease: does dyslipidemia in systemic AA amyloidosis differ from the dyslipidemia in primary glomerulonephritis?

The role of mammalian target of rapamycin pathway in the pathogenesis of pauci-immune glomerulonephritis

Clinical and histopathologic profile of patients with primary IgA nephropathy seen in a tertiary hospital in India

Lupus glomerulonephritis in 788 Chinese children: a multi-centre clinical and histopathological analysis based on 549 renal biopsies

Recent advances in IgG4-related kidney disease

Monoclonal immunoglobulin-associated proliferative glomerulonephritis characterized by organized deposits of striated ultra-substructures: A case report

Diffuse membranoproliferative glomerulonephritis with focal sclerosis and renal amyloidosis in an adult male with autosomal dominant dystrophic epidermolysis bullosa: a case report

Familial risks of glomerulonephritis - a nationwide family study in Sweden

Circulating immune-complexes and complement activation through the classical pathway in myeloperoxidase-ANCA-associated glomerulonephritis

Outcomes of normotensive IgA nephropathy patients with mild proteinuria who have impaired renal function

Efficacy of antisense monocyte chemoattractant protein-1 (MCP-1) in a rat model of mesangial proliferative glomerulonephritis

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