Yuji Ohnishi
Ube, Japan
Last Updated: 09/26/2026
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Found 23 publications
Interleukin-33/ST2 axis in Kawasaki disease: biology, vascular pathology, and future therapeutic strategies.
Journal: Expert review of clinical immunology
Published: April 01, 2026
Early Detection of Acute Myocarditis in the Pediatric Population Using Clinically Accessible Data.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: March 02, 2025
Hypoxic Spell in Pediatric Patient With Repaired Tetralogy of Fallot.
Journal: Circulation reports
Published: September 09, 2024
Necrotic Change of Tunica Media Plays a Key Role in the Development of Coronary Artery Lesions in Kawasaki Disease.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: August 07, 2024
Quantitative serum proteomics to identify candidate biomarkers of coronary artery lesions in Kawasaki disease.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: July 21, 2024
Compound mutations in a patient with congenital long QT syndrome: Clinical challenges and genetic interpretation.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 29, 2024
Congenital Pulmonary Lymphangiectasia Masked by Postoperative Pulmonary Venous Obstruction in an Infant with Total Anomalous Pulmonary Venous Connection.
Journal: International heart journal
Published: March 31, 2024
Interleukin-33/ST2 Axis as Potential Biomarker and Therapeutic Target in Kawasaki Disease.
Journal: Inflammation
Published: August 08, 2022
Safety and Feasibility of Infliximab Therapy in Children With Kawasaki Disease Who Received Live Vaccinations.
Journal: The Pediatric infectious disease journal
Published: July 27, 2022
Successful Mitral Valve Replacement in an Infant with Neonatal Marfan Syndrome due to a Novel Missense Mutation of the FBN1 Gene.
Journal: International heart journal
Published: July 13, 2022
Third-line therapies in patients with Kawasaki disease refractory to first- and second-line intravenous immunoglobulin therapy.
Journal: World journal of pediatrics : WJP
Published: April 20, 2022
A severe clinical phenotype of Noonan syndrome concomitant with incomplete Cantrell syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: September 21, 2021
Last Updated: 09/26/2026