
Hongmei T. Song
Peking Union Medical College Hospital, Peking Union Medical College
Beijing, China
Beijing, China
Last Updated: 09/26/2026
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Found 46 publications
Long-term follow-up of offspring of mothers with systemic lupus erythematosus: an observational study.
Journal: Clinical rheumatology
Published: October 15, 2025
Landscape of Somatic Mutations in a Large Cohort of Chinese Patients With Immune Dysregulations.
Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: September 18, 2025
Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution.
Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025
Multicenter international cohort study of haploinsufficiency of A20 reveals novel genetic architecture and phenotypic evolution.
Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025
CD14+CXCL10+ monocytes are associated with peripheral immune network alterations in systemic juvenile idiopathic arthritis: From multiple centers.
Journal: Genes & diseases
Published: June 04, 2025
Validation and optimization of classification criteria for childhood-onset systemic lupus erythematosus in a multi-center Chinese cohort.
Journal: Frontiers in immunology
Published: April 14, 2025
Epidemiologic trends of Kawasaki Disease and the potential impact of COVID-19 pandemic in Shanghai from 2018 through 2022.
Journal: Chinese medical journal
Published: March 27, 2025
Kearns-Sayre syndrome presenting with fanconi syndrome: a case report.
Journal: Translational pediatrics
Published: February 28, 2025
Mycophenolate Mofetil versus Cyclophosphamide for Initial Therapy in Childhood-Onset Proliferative Lupus Nephritis: A Prospective, Multicenter, Randomized Trial.
Journal: Journal of the American Society of Nephrology : JASN
Published: January 24, 2025
A novel pathogenic mutation of DDX58 causes Singleton-Merten syndrome.
Journal: Fundamental research
Published: January 20, 2025
Discovery of a selective alpha-kinase 1 inhibitor for the rare genetic disease ROSAH syndrome.
Journal: Nature communications
Published: July 30, 2024
Last Updated: 09/26/2026