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Non-immunosuppressive therapies for childhood IgA nephropathy

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.3057-3065

2021

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A genome-wide association study identifies three new risk loci for Kawasaki disease

Nature genetics, 2012-05, Vol.44 (5), p.517-521

2012

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Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy

Pediatric nephrology (Berlin, West), 2021-04, Vol.36 (4), p.899-908

2021

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Influenza virus vaccination in pediatric nephrotic syndrome significantly reduces rate of relapse and influenza virus infection as assessed in a nationwide survey

Scientific reports, 2021-12, Vol.11 (1), p.23305-23305, Article 23305

2021

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Prognosis and acute complications at the first onset of idiopathic nephrotic syndrome in children: a nationwide survey in Japan (JP-SHINE study)

Nephrology, dialysis, transplantation, 2021-02, Vol.36 (3), p.475-481

2021

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Japan Renal Biopsy Registry: the first nationwide, web-based, and prospective registry system of renal biopsies in Japan

Clinical and experimental nephrology, 2011-08, Vol.15 (4), p.493-503

2011

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An “old and new” complication in a child with nephrotic syndrome: Answers

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.1955-1958

2021

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An “old and new” complication in a child with nephrotic syndrome: Questions

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.1953-1954

2021

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High incidence of idiopathic nephrotic syndrome in East Asian children: a nationwide survey in Japan (JP-SHINE study)

Clinical and experimental nephrology, 2017-08, Vol.21 (4), p.651-657

2017

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Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics

Genetics in medicine, 2016-02, Vol.18 (2), p.180-188

2016

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Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome

American journal of human genetics, 2015-10, Vol.97 (4), p.555-566

2015

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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain

Kidney international, 2014-05, Vol.85 (5), p.1208-1213

2014

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Epidemiology of biopsy-proven Henoch–Schönlein purpura nephritis in children: A nationwide survey in Japan

PloS one, 2022-07, Vol.17 (7), p.e0270796-e0270796

2022

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Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Scientific reports, 2020-08, Vol.10 (1), p.14026-14026, Article 14026

2020

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Japan Renal Biopsy Registry and Japan Kidney Disease Registry: Committee Report for 2009 and 2010

Clinical and experimental nephrology, 2013-04, Vol.17 (2), p.155-173

2013

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Cyclosporin A Treatment for Kawasaki Disease Refractory to Initial and Additional Intravenous Immunoglobulin

The Pediatric infectious disease journal, 2011-10, Vol.30 (10), p.871-876

2011

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Validity of the Oxford classification of IgA nephropathy in children

Pediatric nephrology (Berlin, West), 2012-05, Vol.27 (5), p.783-792

2012

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The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults

Kidney international, 2010-05, Vol.77 (10), p.921-927

2010

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Renal disease in the elderly and the very elderly Japanese: analysis of the Japan Renal Biopsy Registry (J-RBR)

Clinical and experimental nephrology, 2012-12, Vol.16 (6), p.903-920

2012

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Crescentic IgA nephropathy in children

Pediatric nephrology (Berlin, West), 2020-06, Vol.35 (6), p.1005-1014

2020

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Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study)

Pediatric nephrology (Berlin, West), 2019-05, Vol.34 (5), p.837-846

2019

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Segmental membranous nephropathy with severe IgG3 deposition

Pediatrics international, 2018-06, Vol.60 (6), p.597-598

2018

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Clinical manifestations of Henoch–Schönlein purpura nephritis and IgA nephropathy: comparative analysis of data from the Japan Renal Biopsy Registry (J-RBR)

Clinical and experimental nephrology, 2016-08, Vol.20 (4), p.552-560

2016

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Efficacy of combination therapy for childhood complicated focal IgA nephropathy

Clinical and experimental nephrology, 2022-06, Vol.26 (6), p.561-570

2022

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Natural history of genetically proven autosomal recessive Alport syndrome

Pediatric nephrology (Berlin, West), 2014-09, Vol.29 (9), p.1535-1544

2014

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Non-immunosuppressive therapies for childhood IgA nephropathy

A genome-wide association study identifies three new risk loci for Kawasaki disease

Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy

Influenza virus vaccination in pediatric nephrotic syndrome significantly reduces rate of relapse and influenza virus infection as assessed in a nationwide survey

Prognosis and acute complications at the first onset of idiopathic nephrotic syndrome in children: a nationwide survey in Japan (JP-SHINE study)

Japan Renal Biopsy Registry: the first nationwide, web-based, and prospective registry system of renal biopsies in Japan

An “old and new” complication in a child with nephrotic syndrome: Answers

An “old and new” complication in a child with nephrotic syndrome: Questions

High incidence of idiopathic nephrotic syndrome in East Asian children: a nationwide survey in Japan (JP-SHINE study)

Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain

Epidemiology of biopsy-proven Henoch–Schönlein purpura nephritis in children: A nationwide survey in Japan

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Japan Renal Biopsy Registry and Japan Kidney Disease Registry: Committee Report for 2009 and 2010

Cyclosporin A Treatment for Kawasaki Disease Refractory to Initial and Additional Intravenous Immunoglobulin

Validity of the Oxford classification of IgA nephropathy in children

The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults

Renal disease in the elderly and the very elderly Japanese: analysis of the Japan Renal Biopsy Registry (J-RBR)

Crescentic IgA nephropathy in children

Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study)

Segmental membranous nephropathy with severe IgG3 deposition

Clinical manifestations of Henoch–Schönlein purpura nephritis and IgA nephropathy: comparative analysis of data from the Japan Renal Biopsy Registry (J-RBR)

Efficacy of combination therapy for childhood complicated focal IgA nephropathy

Natural history of genetically proven autosomal recessive Alport syndrome

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