Xi Yang

Ministry Of Education Key Laboratory Of Child Development And Disorders
Chongqing, China

Last Updated: 09/26/2026

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Found 12 publications

2016 sJIA-MAS criteria and a step-up therapeutic approach in KD-MAS: insights from a combined cohort and literature review.

2016 sJIA-MAS criteria and a step-up therapeutic approach in KD-MAS: insights from a combined cohort and literature review.

Journal: RMD open

Published: November 12, 2025

CD14+CXCL10+ monocytes are associated with peripheral immune network alterations in systemic juvenile idiopathic arthritis: From multiple centers.

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.

Clinical and genetic features of UNC13D deficiency with hypogammaglobulinemia.

Journal: Frontiers in immunology

Published: May 14, 2025

Efficacy of upadacitinib in treating a paediatric case of refractory Takayasu arteritis.

Efficacy of upadacitinib in treating a paediatric case of refractory Takayasu arteritis.

Journal: Rheumatology (Oxford, England)

Published: February 08, 2025

Comparative evaluation of competency-based and real-patient education in undergraduate clinical clerkships: insights from student feedback and performance.

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

Clinical and genetic analysis of macrophage activation syndrome complicating juvenile idiopathic inflammatory myopathies.

Clinical and genetic analysis of macrophage activation syndrome complicating juvenile idiopathic inflammatory myopathies.

Journal: Pediatric research

Published: March 21, 2024

Atypical familial hemophagocytic lymphohistiocytosis type 3 in children: A report of cases and literature review.

Atypical familial hemophagocytic lymphohistiocytosis type 3 in children: A report of cases and literature review.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: November 24, 2023

Inherited CARD9 Deficiency Due to a Founder Effect in East Asia.

Inherited CARD9 Deficiency Due to a Founder Effect in East Asia.

Journal: Journal of clinical immunology

Published: October 11, 2023

A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.

A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.

Journal: Journal of clinical immunology

Published: December 30, 2022

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.

Journal: Journal of clinical immunology

Published: October 30, 2021

UNC13D mutation in a patient with juvenile polymyositis with recurrent macrophage activation syndrome.

UNC13D mutation in a patient with juvenile polymyositis with recurrent macrophage activation syndrome.

Journal: Rheumatology (Oxford, England)

Published: December 16, 2020

X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.

X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.

Journal: European journal of pediatrics

Published: March 15, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026