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Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance

Diabetes (New York, N.Y.), 2017-10, Vol.66 (10), p.2713-2723

2017

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Reduction in urinary angiotensinogen levels and improvement of proteinuria by renin–angiotensin system blockade in pediatric chronic kidney disease patients with very low birth weight

Pediatric nephrology (Berlin, West), 2020-07, Vol.35 (7), p.1307-1314

2020

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Proteinuria and glomerular hypertrophy in extremely low-birthweight children

Pediatrics international, 2014-12, Vol.56 (6), p.860-864

2014

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Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Pediatric diabetes, 2017-11, Vol.18 (7), p.532-539

2017

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End-stage renal disease in Japanese children: a nationwide survey during 2006–2011

Clinical and experimental nephrology, 2015-10, Vol.19 (5), p.933-938

2015

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The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies

The journal of clinical endocrinology and metabolism, 2010-12, Vol.95 (12), p.E511-E518

2010

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Complete oculocerebrorenal phenotype of Lowe syndrome in a female patient with half reduction of inositol polyphosphate 5-phosphatase

CEN case reports, 2020-05, Vol.9 (2), p.95-100

2020

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The true distribution volume and bioavailability of mizoribine in children with chronic kidney disease

Clinical and experimental nephrology, 2017-10, Vol.21 (5), p.884-888

2017

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Population pharmacokinetics of mizoribine in pediatric patients with kidney disease

Clinical and experimental nephrology, 2016-10, Vol.20 (5), p.757-763

2016

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Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157

Pediatrics international, 2009-04, Vol.51 (2), p.216-219

2009

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A further case of renal tubular dysgenesis surviving the neonatal period

European journal of pediatrics, 2009-02, Vol.168 (2), p.207-209

2009

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Risk factors for developing severe clinical course in HUS patients: a national survey in Japan

Pediatrics international, 2008-08, Vol.50 (4), p.441-446

2008

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Evaluation of Limited Sampling Designs to Estimate Maximal Concentration and Area under the Curve of Mizoribine in Pediatric Patients with Renal Disease

Drug metabolism and pharmacokinetics, 2011-01, Vol.26 (1), p.71-78

2011

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The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome

Journal of bone and mineral metabolism, 2005-05, Vol.23 (3), p.231-237

2005

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NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

Pediatric nephrology (Berlin, West), 2003-05, Vol.18 (5), p.412-416

2003

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Developmental Origins of Health and Disease（DOHaD）—The effects of embryonic and infantile environment on kidney disease

Japanese journal of pediatric nephrology, 2014, Vol.26(2), pp.250-255

Satomura, Kenichi

2014

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Evaluation of Limited Sampling Designs to Estimate Maximal Concentration and Area under the Curve of Mizoribine in Pediatric Patients with Renal Disease

DRUG METABOLISM AND PHARMACOKINETICS, 2011, Vol.26 (1), p.71-78

2011

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Benefits of incorporating urinary protein/creatinine ratio measurement in a school urine screening system: The experience of restructuring the school urinary screening system in Osaka Prefecture, Japan

Nephrology (Carlton, Vic.), 2019-11, Vol.24 (11), p.1142-1147

2019

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Association between low birth weight and childhood-onset chronic kidney disease in Japan: a combined analysis of a nationwide survey for paediatric chronic kidney disease and the National Vital Statistics Report

Nephrology, dialysis, transplantation, 2016-11, Vol.31 (11), p.1895-1900

2016

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Identification of CUBN variants in triplets with a 20-year history of proteinuria

CEN case reports, 2024-08

2024

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Molecular and clinical features of K ATP -channel neonatal diabetes mellitus in Japan

Pediatric diabetes, 2017-11, Vol.18 (7), p.532-539

2017

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Progression to end-stage kidney disease in Japanese children with chronic kidney disease: results of a nationwide prospective cohort study

Nephrology, dialysis, transplantation, 2014-04, Vol.29 (4), p.878-884

2014

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Risk factors associated with a decreased estimated glomerular filtration rate based on cystatin C levels in school‐age children with extremely low birthweight

Nephrology (Carlton, Vic.), 2017-06, Vol.22 (6), p.463-469

2017

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Insignificant impact of VUR on the progression of CKD in children with CAKUT

Pediatric nephrology (Berlin, West), 2016-01, Vol.31 (1), p.105-112

2016

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Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

Kidney international, 2005-04, Vol.67 (4), p.1248-1255

2005

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Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance

Reduction in urinary angiotensinogen levels and improvement of proteinuria by renin–angiotensin system blockade in pediatric chronic kidney disease patients with very low birth weight

Proteinuria and glomerular hypertrophy in extremely low-birthweight children

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

End-stage renal disease in Japanese children: a nationwide survey during 2006–2011

The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies

Complete oculocerebrorenal phenotype of Lowe syndrome in a female patient with half reduction of inositol polyphosphate 5-phosphatase

The true distribution volume and bioavailability of mizoribine in children with chronic kidney disease

Population pharmacokinetics of mizoribine in pediatric patients with kidney disease

Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157

A further case of renal tubular dysgenesis surviving the neonatal period

Risk factors for developing severe clinical course in HUS patients: a national survey in Japan

Evaluation of Limited Sampling Designs to Estimate Maximal Concentration and Area under the Curve of Mizoribine in Pediatric Patients with Renal Disease

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

Developmental Origins of Health and Disease（DOHaD）—The effects of embryonic and infantile environment on kidney disease

Evaluation of Limited Sampling Designs to Estimate Maximal Concentration and Area under the Curve of Mizoribine in Pediatric Patients with Renal Disease

Benefits of incorporating urinary protein/creatinine ratio measurement in a school urine screening system: The experience of restructuring the school urinary screening system in Osaka Prefecture, Japan

Association between low birth weight and childhood-onset chronic kidney disease in Japan: a combined analysis of a nationwide survey for paediatric chronic kidney disease and the National Vital Statistics Report

Identification of CUBN variants in triplets with a 20-year history of proteinuria

Molecular and clinical features of K ATP -channel neonatal diabetes mellitus in Japan

Progression to end-stage kidney disease in Japanese children with chronic kidney disease: results of a nationwide prospective cohort study

Risk factors associated with a decreased estimated glomerular filtration rate based on cystatin C levels in school‐age children with extremely low birthweight

Insignificant impact of VUR on the progression of CKD in children with CAKUT

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

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