Kentaro Toyota

Yamagata, Japan

Last Updated: 09/26/2026

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Found 10 publications

Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017.

Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017.

Journal: Japanese journal of infectious diseases

Published: December 04, 2018

Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.

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.

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

Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia.

Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia.

Journal: Molecular genetics and metabolism reports

Published: December 13, 2013

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

Journal: Journal of the peripheral nervous system : JPNS

Published: March 26, 2013

A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy.

A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy.

Journal: Journal of human genetics

Published: February 15, 2013

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.

Journal: Journal of human genetics

Published: September 28, 2012

An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene.

An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene.

Journal: Internal medicine (Tokyo, Japan)

Published: August 16, 2012

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.

Journal: Journal of human genetics

Published: March 23, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026