Yuta Ichikawa

Kobe, Japan

Last Updated: 09/26/2026

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Found 22 publications

Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants.

Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants.

Journal: Kidney international reports

Published: December 12, 2025

Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease.

Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease.

Journal: Clinical and experimental nephrology

Published: March 04, 2025

Potential involvement of abnormal splicing in severe WT1-related disorders.

Potential involvement of abnormal splicing in severe WT1-related disorders.

Journal: Clinical and experimental nephrology

Published: February 06, 2025

Prolonged hypokalemia long after causative factor elimination in pseudo-Bartter/Gitelman syndrome.

Prolonged hypokalemia long after causative factor elimination in pseudo-Bartter/Gitelman syndrome.

Journal: Clinical and experimental nephrology

Published: February 05, 2025

Co-localization of IgG with nephrin in immune-mediated idiopathic nephrotic syndrome.

Co-localization of IgG with nephrin in immune-mediated idiopathic nephrotic syndrome.

Journal: Clinical and experimental nephrology

Published: January 24, 2025

Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort.

Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort.

Journal: Clinical and experimental nephrology

Published: December 11, 2024

Differences in kidney prognosis between congenital and infantile nephrotic syndrome.

Differences in kidney prognosis between congenital and infantile nephrotic syndrome.

Journal: Pediatric nephrology (Berlin, Germany)

Published: October 12, 2024

Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions.

Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions.

Journal: Kidney international reports

Published: September 08, 2024

Response to Dr. Fujinaga and Dr. Watanabe: what is the most appropriate cut-off for hypoalbuminemia in nephrotic syndrome?

Response to Dr. Fujinaga and Dr. Watanabe: what is the most appropriate cut-off for hypoalbuminemia in nephrotic syndrome?

Journal: Pediatric nephrology (Berlin, Germany)

Published: August 28, 2024

Saline versus balanced crystalloids for hydration post-kidney biopsy.

Saline versus balanced crystalloids for hydration post-kidney biopsy.

Journal: Pediatric nephrology (Berlin, Germany)

Published: July 26, 2024

Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.

Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: April 21, 2024

Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome.

Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome.

Journal: Kidney360

Published: April 16, 2024

Showing 1-12 of 22

Last Updated: 09/26/2026