• <em>Pneumocystis murina</em> lesions in lungs of experimentally infected Cd40l^-/- mice
• A case of secondary multiple evanescent white dot syndrome in a patient with preexisting wet age-related macular degeneration
• A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese families
• A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome
• A single-center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class- Switch Recombination defects
• Advanced computational analysis of CD40LG variants in atypical X-linked hyper-IgM syndrome
• Antibody Response Before and After the Booster Dose of Inactivated Corona Vaccine in Antibody Deficient Patients
• Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I
• CD40L Activates Platelet Integrin αIIbβ3 by Binding to the Allosteric Site (Site 2) in a KGD-Independent Manner and HIGM1 Mutations Are Clustered in the Integrin-Binding Sites of CD40L
• CD40LG-associated X-linked Hyper-IgM Syndrome (XHIGM) with pulmonary alveolar proteinosis: a case report
• Characterization of a mouse model of ICF syndrome reveals enhanced CD19 activation in inducing hypogammaglobulinemia
• Clinical and Immunological Features, Genetic Variants, and Outcomes of Patients with CD40 Deficiency
• Clinical practice guideline for activated phosphatidyl inositol 3-kinase-delta syndrome in Japan
• Compound Heterozygosity in Hyper-IgM Syndrome Type 3: Case Report and Literature Review
• Compound Heterozygosity in Hyper‑IgM Syndrome Type 3: Case Report and Literature Review
• Elevated levels of enteric IgA in an unimmunised mouse model of Hyper IgM syndrome derived from gut-associated secondary lymph organs even in the absence of germinal centres
• Enhanced CD19 activity in B cells contributes to immunodeficiency in mice deficient in the ICF syndrome gene Zbtb24
• Gene regulation in inborn errors of immunity: Implications for gene therapy design and efficacy
• Hematopoietic stem cell Transplantation in Children with very Early Onset Inflammatory Bowel Disease Secondary to Monogenic Disorders of immune-dysregulation
• Hyper-IgM and acquired C1q complement deficiency in a patient with <em>de novo</em>  <em>ATM</em> mutation
• Hyper-IgM syndrome with early liver involvement
• Hyper-Immunoglobulin E (IgE) Syndrome: A Diagnostic Dilemma
• Hyper-Reactive Malarial Splenomegaly Syndrome (HMSS)
• Immunodeficiency
• Immunoglobulin class-switch recombination: Mechanism, regulation, and related diseases
• Intramural Duodenal Hematoma in a Case of Hyper IgM Syndrome
• Late diagnosis of X-linked hyper-IgM syndrome presenting as community-acquired Pseudomonas aeruginosa pneumonia-related septic shock
• Late-Onset Lymphopenia and ITP in a Patient with Hyper IgM Syndrome Due to a Homozygous Variant in AICDA
• Mechanotransduction governs CD40 function and underlies X-linked Hyper IgM syndrome
• Orbital apex syndrome secondary to Pseudomonas aeruginosa sinusitis in a child with hyperimmunoglobulin M syndrome
• Progressive Multifocal Leukoencephalopathy With Hyper-IgM Syndrome in a 6-Year-Old Boy
• SARS-CoV-2 Antibody Titers and Severity of Multisystem Inflammatory Syndrome in Children
• Two cases of successful sirolimus treatment for patients with activated phosphoinositide 3-kinase delta syndrome 1
• Two cases of successful sirolimus treatment for patients with activated phosphoinositide 3-kinase δ syndrome 1
• Type 2 hyper-IgM syndrome with a rare variant of AICDA gene mutation in a young woman
• Use of Metagenomic Next-Generation Sequencing in the Identification of Pneumocystis Jiroveci Pneumonia in a Previously Healthy Infant Diagnosed With X-Linked Hyper-IgM Syndrome
• Who's your data? Primary immune deficiency differential diagnosis prediction via machine learning and data mining of the USIDNET registry
• X-Linked Immunodeficiency