Hidenori Yamamoto
Nagoya, Japan
Last Updated: 09/26/2026
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Found 19 publications
Dynamic digital radiography as a minimally invasive alternative to perfusion scintigraphy for assessing pulmonary blood flow in children: a prospective study.
Journal: Pediatric radiology
Published: December 20, 2025
Oncogenic Signaling Activation and Potential Biomarkers in Congestive Hepatopathy Revealed by Proteomic Analysis.
Journal: Hepatology research : the official journal of the Japan Society of Hepatology
Published: December 11, 2025
Neonatal case of congenital dilated cardiomyopathy, cholestatic liver injury, and hyperferritinemia with FHL2 variant: a case report suggesting possible novel phenotypes.
Journal: Cardiology in the young
Published: October 03, 2025
Persistent complete atrioventricular block in an infant with Kawasaki disease: a rare case report.
Journal: Cardiology in the young
Published: July 31, 2025
A familial case of aortic dilatation with p.Tyr470Cys in TGFBR2 in which the phenotype included only vascular lesions.
Journal: Cardiology in the young
Published: October 04, 2024
Frequency of SARS-CoV-2 antecedent infection in patients with Kawasaki disease.
Journal: Nagoya journal of medical science
Published: April 02, 2024
Dysbiosis of gut microbiota in patients with protein-losing enteropathy after the Fontan procedure.
Journal: International journal of cardiology
Published: July 13, 2023
Case report: High-dose epoprostenol therapy in pediatric patients with pulmonary hypertension and developmental lung disease.
Journal: Frontiers in pediatrics
Published: December 05, 2022
Tension hemothorax 1 week after pericardiocentesis associated with thrombocytopenia.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: July 07, 2022
Conception by assisted reproductive technology in infants with critical congenital heart disease in Japan.
Journal: Reproductive biomedicine online
Published: March 30, 2021
Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor.
Journal: The Journal of allergy and clinical immunology
Published: October 26, 2020
Familial cardiac septal defect due to a novel nine-base deletion in TBX20.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: September 16, 2020
Last Updated: 09/26/2026