Yutaka Nishimura

Hiroshima, Japan

Last Updated: 09/26/2026

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Found 11 publications

Neonatal Stroke Following Placental Abruption in a Protein C-Deficient Mother-Infant Pair.

Neonatal Stroke Following Placental Abruption in a Protein C-Deficient Mother-Infant Pair.

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

Published: October 05, 2025

Sildenafil for bronchopulmonary dysplasia-associated pulmonary hypertension: A systematic search and narrative synthesis.

Sildenafil for bronchopulmonary dysplasia-associated pulmonary hypertension: A systematic search and narrative synthesis.

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

Published: July 25, 2025

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site.

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site.

Journal: Clinical epigenetics

Published: July 14, 2025

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Journal: Clinical epigenetics

Published: May 13, 2024

Prophylactic sildenafil to prevent bronchopulmonary dysplasia: A systematic review and meta-analysis.

Prophylactic sildenafil to prevent bronchopulmonary dysplasia: A systematic review and meta-analysis.

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

Published: October 23, 2023

Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine Remethylation.

Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine Remethylation.

Journal: International journal of neonatal screening

Published: May 28, 2021

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation.

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation.

Journal: Science advances

Published: August 06, 2020

Novel PHOX2B mutations in congenital central hypoventilation syndrome.

Novel PHOX2B mutations in congenital central hypoventilation syndrome.

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

Published: July 15, 2018

Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with Thrombocytopenia.

Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with Thrombocytopenia.

Journal: The Journal of investigative dermatology

Published: May 20, 2017

Effects of the early administration of sivelestat sodium on bronchopulmonary dysplasia in infants: A retrospective cohort study.

Effects of the early administration of sivelestat sodium on bronchopulmonary dysplasia in infants: A retrospective cohort study.

Journal: Early human development

Published: March 06, 2017

A Quality Improvement Collaborative Program for Neonatal Pain Management in Japan.

A Quality Improvement Collaborative Program for Neonatal Pain Management in Japan.

Journal: Advances in neonatal care : official journal of the National Association of Neonatal Nurses

Published: January 24, 2017

Showing 1-11 of 11

Last Updated: 09/26/2026