Taeko Hashimoto
Yamagata, Japan
Last Updated: 09/26/2026
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Found 15 publications
Early-onset kidney failure in a girl with autosomal dominant tubulointerstitial kidney disease due to a de novo UMOD variant.
Journal: CEN case reports
Published: September 14, 2025
Investigation of clinical and genetic characteristics of Alport syndrome using a national registry in Japan (JP-ALPS).
Journal: Clinical and experimental nephrology
Published: April 15, 2025
Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: February 02, 2022
Response to steroid and immunosuppressive therapies may predict post-transplant recurrence of steroid-resistant nephrotic syndrome.
Journal: Pediatric transplantation
Published: April 19, 2021
Degree of foot process effacement in patients with genetic focal segmental glomerulosclerosis: a single-center analysis and review of the literature.
Journal: Scientific reports
Published: February 01, 2021
Laminin β2 variants associated with isolated nephropathy that impact matrix regulation.
Journal: JCI insight
Published: November 10, 2020
A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report.
Journal: BMC nephrology
Published: September 25, 2020
In Vivo Expression of NUP93 and Its Alteration by NUP93 Mutations Causing Focal Segmental Glomerulosclerosis.
Journal: Kidney international reports
Published: March 17, 2019
Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.
Journal: Journal of human genetics
Published: August 26, 2016
Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.
Journal: Journal of human genetics
Published: April 07, 2015
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.
Journal: Journal of human genetics
Published: July 30, 2014
Therapeutic target for nephrotic syndrome: Identification of novel slit diaphragm associated molecules.
Journal: World journal of nephrology
Published: March 26, 2014
Last Updated: 09/26/2026