Zhiyong Y. Zhang
Chongqing, China
Last Updated: 09/26/2026
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Found 53 publications
Clinical characteristics, autoantibody profiles, and therapeutic outcomes of juvenile systemic sclerosis: an 11-year single-center experience from China.
Journal: Frontiers in immunology
Published: February 26, 2026
Development and Validation of a Rapid Benefit-Risk Assessment Index for Pediatric Off-Label Drug Use.
Journal: Journal of evidence-based medicine
Published: January 23, 2026
Research progress of upadacitinib in the treatment pediatric rheumatic and autoimmune diseases
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: January 15, 2026
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
Clinical and genetic features of UNC13D deficiency with hypogammaglobulinemia.
Journal: Frontiers in immunology
Published: May 14, 2025
Novel compound heterozygous MRTFA gene variants cause multiple dysfunctions of neutrophils and autoinflammation.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: May 09, 2025
Efficacy of upadacitinib in treating a paediatric case of refractory Takayasu arteritis.
Journal: Rheumatology (Oxford, England)
Published: February 08, 2025
Characteristics of Mycobacterial, COVID-19, and Talaromyces Marneffei Infections in Patients with IL12RB1 and IFNGR1 Mutations in Western China.
Journal: Journal of clinical immunology
Published: January 08, 2025
Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation.
Journal: Frontiers in immunology
Published: December 13, 2024
Comparative evaluation of competency-based and real-patient education in undergraduate clinical clerkships: insights from student feedback and performance.
Journal: BMC medical education
Published: July 16, 2024
Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation.
Journal: Frontiers in immunology
Published: July 07, 2024
Last Updated: 09/26/2026