Kenji Yamada

Himebara, Japan

Last Updated: 09/26/2026

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Found 44 publications

A Japanese Boy With Spotted Fever and Overlapping Symptoms of Kawasaki Disease: A Case Report.

A Japanese Boy With Spotted Fever and Overlapping Symptoms of Kawasaki Disease: A Case Report.

Journal: Cureus

Published: January 06, 2024

Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype.

Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype.

Journal: Molecular genetics and metabolism reports

Published: November 09, 2022

The frequencies of very long-chain acyl-CoA dehydrogenase deficiency genetic variants in Japan have changed since the implementation of expanded newborn screening.

The frequencies of very long-chain acyl-CoA dehydrogenase deficiency genetic variants in Japan have changed since the implementation of expanded newborn screening.

Journal: Molecular genetics and metabolism

Published: November 04, 2021

Ophthalmic herpes zoster.

Ophthalmic herpes zoster.

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

Published: September 05, 2021

Long-Term Neurological Outcomes of Adult Patients with Phenylketonuria before and after Newborn Screening in Japan.

Long-Term Neurological Outcomes of Adult Patients with Phenylketonuria before and after Newborn Screening in Japan.

Journal: International journal of neonatal screening

Published: March 03, 2021

The perioperative transition of serum biomarkers of a 1.5-year-old boy with very-long-chain acyl-CoA dehydrogenase deficiency.

The perioperative transition of serum biomarkers of a 1.5-year-old boy with very-long-chain acyl-CoA dehydrogenase deficiency.

Journal: Molecular genetics and metabolism reports

Published: February 25, 2021

Template Stripping Method-Based Au Nanoarray for Surface-Enhanced Raman Scattering Detection of Antiepileptic Drug.

Template Stripping Method-Based Au Nanoarray for Surface-Enhanced Raman Scattering Detection of Antiepileptic Drug.

Journal: Micromachines

Published: August 31, 2020

Long-Term Outcomes of Adult Patients with Homocystinuria before and after Newborn Screening.

Long-Term Outcomes of Adult Patients with Homocystinuria before and after Newborn Screening.

Journal: International journal of neonatal screening

Published: July 01, 2020

Efficacy of bezafibrate for preventing myopathic attacks in patients with very long-chain acyl-CoA dehydrogenase deficiency.

Efficacy of bezafibrate for preventing myopathic attacks in patients with very long-chain acyl-CoA dehydrogenase deficiency.

Journal: Brain & development

Published: April 01, 2020

Need for strict clinical management of patients with carnitine palmitoyltransferase II deficiency: Experience with two cases detected by expanded newborn screening.

Need for strict clinical management of patients with carnitine palmitoyltransferase II deficiency: Experience with two cases detected by expanded newborn screening.

Journal: Molecular genetics and metabolism reports

Published: March 30, 2020

Late-onset argininosuccinic aciduria associated with hyperammonemia triggered by influenza infection in an adolescent: A case report.

Late-onset argininosuccinic aciduria associated with hyperammonemia triggered by influenza infection in an adolescent: A case report.

Journal: Molecular genetics and metabolism reports

Published: March 14, 2020

Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriers.

Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriers.

Journal: Molecular genetics and metabolism reports

Published: September 11, 2019

Showing 1-12 of 44

Last Updated: 09/26/2026