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Rituximab therapy for refractory steroid-resistant nephrotic syndrome in children

Pediatric nephrology (Berlin, West), 2020-01, Vol.35 (1), p.17-24

2020

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Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

The Lancet (British edition), 2014-10, Vol.384 (9950), p.1273-1281

2014

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A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

Journal of human genetics, 2020-08, Vol.65 (8), p.705-709

2020

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Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome

The journal of obstetrics and gynaecology research, 2023-06, Vol.49 (6), p.1624-1627

2023

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Rituximab for nephrotic syndrome in children

Clinical and Experimental Nephrology, 2017-04, Vol.21 (2), p.193-202

2017

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The association between prehospital vital signs of children and their critical clinical outcomes at hospitals

Scientific reports, 2022-03, Vol.12 (1), p.5199-7, Article 5199

2022

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Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome

Scientific reports, 2022-01, Vol.12 (1), p.969-969, Article 969

2022

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A review of clinical characteristics and genetic backgrounds in Alport syndrome

Clinical and experimental nephrology, 2019-02, Vol.23 (2), p.158-168

2019

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Branchio-oto-renal syndrome: Comprehensive review based on nationwide surveillance in Japan

Pediatrics international, 2014-06, Vol.56 (3), p.309-314

2014

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Role of Wnt5a-Ror2 Signaling in Morphogenesis of the Metanephric Mesenchyme during Ureteric Budding

Molecular and cellular biology, 2014-08, Vol.34 (16), p.3096-3105

2014

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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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Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

Scientific reports, 2020-01, Vol.10 (1), p.270-270, Article 270

2020

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Prevalence of Wilson disease based on genome databases in Japan

Pediatrics international, 2021-08, Vol.63 (8), p.918-922

2021

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Homozygous splicing mutation in NUP133 causes Galloway–Mowat syndrome

Annals of neurology, 2018-12, Vol.84 (6), p.814-828

2018

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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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Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome

Journal of nephrology, 2019-02, Vol.32 (1), p.155-159

2019

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Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

Scientific reports, 2021-08, Vol.11 (1), p.16099-16099, Article 16099

2021

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Epidemiology and clinical features of childhood-onset anti-neutrophil cytoplasmic antibody–associated vasculitis: a clinicopathological analysis

Pediatric nephrology (Berlin, West), 2019-08, Vol.34 (8), p.1425-1433

2019

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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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Bilirubin/albumin (B/A) ratios correlate with unbound bilirubin levels in preterm infants

Pediatric research, 2021-05, Vol.89 (6), p.1427-1431

2021

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Diagnostic and clinical significance of the titin fragment in urine of Duchenne muscular dystrophy patients

Clinica chimica acta, 2018-01, Vol.476, p.111-116

2018

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Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children

Journal of autism and developmental disorders, 2022-02, Vol.52 (2), p.483-489

2022

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Mild progressive osseous heteroplasia overlap syndrome with PTH and TSH resistance appearing during adolescence and not early childhood

Endocrine, 2021-12, Vol.74 (3), p.685-689

2021

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Rituximab for childhood refractory nephrotic syndrome

Pediatrics international, 2011-10, Vol.53 (5), p.617-621

Iijima, Kazumoto

2011

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Neurological outcomes in symptomatic congenital cytomegalovirus-infected infants after introduction of newborn urine screening and antiviral treatment

Brain & development (Tokyo. 1979), 2016-02, Vol.38 (2), p.209-216

2016

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Rituximab therapy for refractory steroid-resistant nephrotic syndrome in children

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome

Rituximab for nephrotic syndrome in children

The association between prehospital vital signs of children and their critical clinical outcomes at hospitals

Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome

A review of clinical characteristics and genetic backgrounds in Alport syndrome

Branchio-oto-renal syndrome: Comprehensive review based on nationwide surveillance in Japan

Role of Wnt5a-Ror2 Signaling in Morphogenesis of the Metanephric Mesenchyme during Ureteric Budding

Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

Prevalence of Wilson disease based on genome databases in Japan

Homozygous splicing mutation in NUP133 causes Galloway–Mowat syndrome

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

Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome

Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

Epidemiology and clinical features of childhood-onset anti-neutrophil cytoplasmic antibody–associated vasculitis: a clinicopathological analysis

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

Bilirubin/albumin (B/A) ratios correlate with unbound bilirubin levels in preterm infants

Diagnostic and clinical significance of the titin fragment in urine of Duchenne muscular dystrophy patients

Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children

Mild progressive osseous heteroplasia overlap syndrome with PTH and TSH resistance appearing during adolescence and not early childhood

Rituximab for childhood refractory nephrotic syndrome

Neurological outcomes in symptomatic congenital cytomegalovirus-infected infants after introduction of newborn urine screening and antiviral treatment

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