Katsuyuki Yokoi

Okazaki, Japan

Last Updated: 09/26/2026

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Found 15 publications

Acute Scrotal Involvement in Kawasaki Disease: A Potential Clinical Clue to Persistent Disease Activity.

Acute Scrotal Involvement in Kawasaki Disease: A Potential Clinical Clue to Persistent Disease Activity.

Journal: Case reports in pediatrics

Published: May 29, 2026

Respiratory Pathogen Detection in Pediatric Asthma Exacerbations Using the FilmArray Respiratory Panel 2.1.

Respiratory Pathogen Detection in Pediatric Asthma Exacerbations Using the FilmArray Respiratory Panel 2.1.

Journal: Journal of medical virology

Published: March 26, 2026

Improvement of propionic acidemia-associated dilated cardiomyopathy through nutritional adjustment and heart failure medication: A case report.

Improvement of propionic acidemia-associated dilated cardiomyopathy through nutritional adjustment and heart failure medication: A case report.

Journal: Journal of cardiology cases

Published: December 21, 2024

An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion.

An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion.

Journal: The Tohoku journal of experimental medicine

Published: September 07, 2022

Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report.

Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report.

Journal: JIMD reports

Published: July 03, 2022

Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes.

Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes.

Journal: The Tohoku journal of experimental medicine

Published: January 27, 2022

Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case report.

Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case report.

Journal: JIMD reports

Published: October 20, 2021

Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disorders.

Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disorders.

Journal: Molecular genetics and metabolism reports

Published: June 20, 2021

Peripheral venous catheter-related candidemia in an immunocompetent child.

Peripheral venous catheter-related candidemia in an immunocompetent child.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: February 27, 2021

Novel ARG1 variants identified in a patient with arginase 1 deficiency.

Novel ARG1 variants identified in a patient with arginase 1 deficiency.

Journal: Human genome variation

Published: November 09, 2020

Impact of DPYD, DPYS, and UPB1 gene variations on severe drug-related toxicity in patients with cancer.

Impact of DPYD, DPYS, and UPB1 gene variations on severe drug-related toxicity in patients with cancer.

Journal: Cancer science

Published: May 19, 2020

Clinical and genetic aspects of mild hypophosphatasia in Japanese patients.

Clinical and genetic aspects of mild hypophosphatasia in Japanese patients.

Journal: Molecular genetics and metabolism reports

Published: July 03, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026