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Publications by Kazumoto Iijima

Mutations in Six Nephrosis Genes Delineate a Pathogenic Pathway Amenable to Treatment

Nature Communications

English

Differential Diagnosis of Bartter Syndrome, Gitelman Syndrome, and Pseudo–Bartter/Gitelman Syndrome Based on Clinical Characteristics

English

Strong Association of theHLA-DR/DQLocus With Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population

Journal of the American Society of Nephrology : JASN

Medicine

Nephrology

2018

English

Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions

Circulation. Genomic and precision medicine

Genetics

Cardiovascular Medicine

Cardiology

2018

English

Epithelial-To-Mesenchymal Transition in Cyst Lining Epithelial Cells in an Orthologous PCK Rat Model of Autosomal-Recessive Polycystic Kidney Disease

American Journal of Physiology - Renal Physiology

Urology

Physiology

2011

English

Aberrant Smad3 Phosphoisoforms in Cyst-Lining Epithelial Cells in the CPK Mouse, a Model of Autosomal Recessive Polycystic Kidney Disease

American Journal of Physiology - Renal Physiology

Urology

Physiology

2017

English

Age-Specific Percentile-Based Reference Curve of Serum Procalcitonin Concentrations in Japanese Preterm Infants

Scientific Reports

Multidisciplinary

2016

English

Treatment of a Case of Severe Insulin Resistance Due to a PIK3R1 Mutation With a Sodium-Glucose Cotransporter-2 Inhibitor

Journal of Diabetes Investigation

English

Yersinia Pseudotuberculosis Infection in Kawasaki Disease and Its Clinical Characteristics

English

The First Report of Adolescent TAFRO Syndrome, a Unique Clinicopathologic Variant of Multicentric Castleman’s Disease

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Kazumoto Iijima

Mutations in Six Nephrosis Genes Delineate a Pathogenic Pathway Amenable to Treatment

Differential Diagnosis of Bartter Syndrome, Gitelman Syndrome, and Pseudo–Bartter/Gitelman Syndrome Based on Clinical Characteristics

Strong Association of theHLA-DR/DQLocus With Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population

Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions

Epithelial-To-Mesenchymal Transition in Cyst Lining Epithelial Cells in an Orthologous PCK Rat Model of Autosomal-Recessive Polycystic Kidney Disease

Aberrant Smad3 Phosphoisoforms in Cyst-Lining Epithelial Cells in the CPK Mouse, a Model of Autosomal Recessive Polycystic Kidney Disease

Age-Specific Percentile-Based Reference Curve of Serum Procalcitonin Concentrations in Japanese Preterm Infants

Treatment of a Case of Severe Insulin Resistance Due to a PIK3R1 Mutation With a Sodium-Glucose Cotransporter-2 Inhibitor

Yersinia Pseudotuberculosis Infection in Kawasaki Disease and Its Clinical Characteristics

The First Report of Adolescent TAFRO Syndrome, a Unique Clinicopathologic Variant of Multicentric Castleman’s Disease