• A novel thymoma-associated immunodeficiency with increased naive T cells and reduced CD247 expression
• An unusual cause for rib osteomyelitis in the tropics: Cryptococcal osteomyelitis
• Assessment of risk factors in pyogenic liver abscesses in children
• Autoimmunity in primary T-cell immunodeficiencies
• Central nervous system manifestations of LRBA deficiency: case report of two siblings and literature review
• Compound heterozygous TYK2 mutations underlie primary immunodeficiency with T-cell lymphopenia
• Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1
• Disturbance in the reconstitution of distinct T-cell subsets and the incidence of GvHD following allo-HSCT in pediatric patients with non-malignant hematological disorders
• Expression and clinical significance of PD-1 in UCEC and its Impact on tumor
• Fatal Severe Cytokine Release Syndrome Post-haploidentical Stem Cell Transplant With Post-transplant Cyclophosphamide in an Infant With Severe Combined Immunodeficiency and Disseminated Bacille Calmette-Guérin Infection
• Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation
• Hemophagocytic inflammatory syndrome in ADA-SCID: report of two cases and literature review
• Human Immunodeficiency Virus 1 Preferentially Fuses with pH-Neutral Endocytic Vesicles in Cell Lines and Human Primary CD4+ T-Cells
• Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (<em>FBP1, ACAD9)</em> and vesicle trafficking <em>(RAB27A)</em>
• Immunologic and Genetic Contributors to CD46-Dependent Immune Dysregulation
• Integrated genetic analyses of immunodeficiency-associated Epstein-Barr virus- (EBV) positive primary CNS lymphomas
• Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility
• Modern management of primary T-cell immunodeficiencies
• Phenotypic variations of cartilage hair hypoplasia: granulomatous skin inflammation and severe T cell immunodeficiency as initial clinical presentation in otherwise well child with short stature
• Primary T-cell immunodeficiency with functional revertant somatic mosaicism in CD247
• Recent advances in understanding the pathophysiology of primary T cell immunodeficiencies
• Relationship of Bone Mineral Density with CD4+ T Cell Counts and Association of Muscle Mass with B Cells in Common Variable Immunodeficiency Patient
• Rethinking immunologic risk: a retrospective cohort study of severe SARS-CoV-2 infections in individuals with congenital immunodeficiencies
• RETRACTED: Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation
• RNA sequencing reveals the consequences of a novel insertion in dedicator of cytokinesis-8
• Role of primary T-cell immunodeficiency and hepatitis B coinfection on spontaneous clearance of hepatitis C: The BC Hepatitis Testers Cohort
• Severe congenital T-lymphocytopenia may affect the outcome of neonatal intensive care
• Short telomere syndromes cause a primary T cell immunodeficiency
• Spontaneous remission of angioimmunoblastic T-cell lymphoma in a child with ataxia-telangiectasia: a case report
• Tap water: A possible source of nontuberculous mycobacterial infection in patients with T cell deficiency
• Unraveling the Role of Toll-like Receptors in the Immunopathogenesis of Selected Primary and Secondary Immunodeficiencies
• α- and β-papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions