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Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|September 18, 2020
The clinical, immunological and genetic features of 12 Chinese patients with STAT3 mutationsLi Lin, Ying Wang, Bijun Sun, et al.Virology Journal|April 2, 2025
Characterization of the epidemiology, susceptibility genes and clinical features of viral infections among children with inborn immune errors: a retrospective studyHaiqiao Zhang, Wenjie Wang, Qinhua Zhou, et al.Journal of Clinical Immunology|June 26, 2024
Novel Mutation in the Moesin (MSN) Gene Leads to Immunodeficiency with Epstein-Barr Virus (EBV) Infection and Dermatomyositis-Like SymptomsBijun Sun, Luyao Liu, Lingli Han, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|April 10, 2025
Invasive fungal disease in a large cohort of hospitalized children with inborn errors of immunity in ChinaHaiqiao Zhang, Mi Yang, Wenjing Ying, et al.Journal of Clinical Immunology|February 28, 2019
Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV ViremiaXiaolong Dong, Luyao Liu, Ying Wang, et al.Clinical and Experimental Immunology|October 15, 2024
Intrinsic functional defects in B cells of patients with NFKB2 mutationsQing Min, Yaxuan Li, Xuzhe Wu, et al.Journal of Clinical Immunology|October 9, 2024
Novel Compound Heterozygous Variants in the FAS Gene Lead to Fetal Onset of Autoimmune Lymphoproliferative Syndrome (ALPS)Qi Wu, Bijun Sun, Jia Hou, et al.Journal of Clinical Immunology|August 2, 2025
A Novel R140S γc Variant Alters Cellular Distribution, Reduces Surface Expression, and Impairs Cytokine Signaling in Atypical X-SCIDLulu Dong, Bijun Sun, Qing Min, et al.Frontiers in Immunology|July 8, 2022
Cellular Mechanisms Underlying B Cell Abnormalities in Patients With Gain-of-Function Mutations in the PIK3CD GeneWenjie Wang, Qing Min, Nannan Lai, et al.Nature|December 13, 2019
A dominant autoinflammatory disease caused by non-cleavable variants of RIPK1Panfeng Tao, Jinqiao Sun, Zheming Wu, et al.Pageof 4