• 18q Deletion Syndrome Presenting with Late-Onset Combined Immunodeficiency
• A Case of Oral Lichen Planus Preceding the Diagnosis of Good Syndrome
• A Cross-Sectional Study of Health-Related Quality of Life in Patients with Predominantly Antibody Deficiency
• A Cross-Sectional Study of Health-Related Quality of Life in Patients with Predominantly Antibody Deficiency
• A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings
• A Nationwide Study of the Delayed Diagnosis and the Clinical Manifestations of Predominantly Antibody Deficiencies and <em>CTLA4</em>-Mediated Immune Dysregulation Syndrome in Greece
• 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 novel HOIP frameshift variant alleviates NF-kappaB signalling and sensitizes cells to TNF-induced death
• A novel IKZF1 variant in a family with autosomal dominant CVID: A case for expanding exon coverage in inborn errors of immunity
• A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency
• A novel splice-site mutation in NFKB1 presenting as common variable immunodeficiency and post-operative hyperinflammation responsive to anti-IL-1 therapy
• A novel splice-site mutation in NFKB1 presenting as common variable immunodeficiency and postoperative hyperinflammation responsive to anti-IL-1 therapy
• A Young Woman with Common Variable Immunodeficiency: The Role of Thorough Medical History and Physical Examination in Accurate Diagnosis
• Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment
• Advancements in Human Norovirus Cultivation in Human Intestinal Enteroids
• Allogeneic Hematopoietic Cell Transplantation Ameliorated Asymptomatic Granulomatous and Lymphocytic Interstitial Lung Disease in a Patient With XIAP Deficiency
• Altered Genome-Wide DNA Methylation in the Duodenum of Common Variable Immunodeficiency Patients
• An Exploratory Approach of Clinically Useful Biomarkers of Cvid by Logistic Regression
• An Immunodeficiency Disorder Presenting in the Neonatal Period
• Analysis of LRBA pathogenic variants and the association with functional protein domains and clinical presentation
• Antibody Response Before and After the Booster Dose of Inactivated Corona Vaccine in Antibody Deficient Patients
• Approach to diagnosing and managing granulomatous-lymphocytic interstitial lung disease
• Aspergillus terreus pulmonary infection in a patient with late-onset combined immunodeficiency: a case report with literature review
• Assessment of Sleep Disorders in Patients with CVID
• Association Between Cytometric Biomarkers, Clinical Phenotype, and Complications of Common Variable Immunodeficiency
• Bifidobacterium and Lactobacillus Probiotics and Gut Dysbiosis in Preterm Infants: The PRIMAL Randomized Clinical Trial
• Case 20-2024: A 73-Year-Old Man with Recurrent Fever and Liver Lesions
• Case Report: Common variable immunodeficiency phenotype and granulomatous-lymphocytic interstitial lung disease with a novel SOCS1 variant
• Central retinal artery occlusion in a child with ADA2 deficiency: a case report
• Changes in health-related quality of life in common variable immunodeficiency: an eight-year journey, including the COVID-19 pandemic
• Characteristics of large granular lymphocyte leukemia associated with variable common immunodeficiency disorders: A study of 12 cases
• Clinical and experimental treatment of primary humoral immunodeficiencies
• Clinical and genetic analysis of trichohepatoneurodevelopmental syndrome caused by a <em>CCDC47</em> variant
• Common Variable Immunodeficiency and Hodgkin Lymphoma in a 50-Year-Old Male
• Common variable immunodeficiency associated enteropathy: A diagnostic enigma in developing countries
• Current Practices and Considerations in Lung Biopsy for Suspected Granulomatous-Lymphocytic Interstitial Lung Disease (GLILD): A Clinician Survey
• Current Practices and Considerations in Lung Biopsy for Suspected Granulomatous-Lymphocytic Interstitial Lung Disease: A Clinician Survey
• Cytomegalovirus drives Vdelta1(+) gammadelta T cell expansion and clonality in common variable immunodeficiency
• Development of hepatic fibrosis in common variable immunodeficiency-related porto-sinusoidal vascular disorder
• Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study
• Dysfunctional mitochondria, disrupted levels of reactive oxygen species, and autophagy in B cells from common variable immunodeficiency patients
• Early Onset Inflammatory Bowel Disease Due to Immunodeficiency as a Result of ICOS Gene Homozygous Mutation
• Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease
• Evaluation of Frequency of CMV Replication and Disease Complications Reveals New Cellular Defects and a Time Dependent Pattern in CVID Patients
• Exploring gastric cancer genetics: A turning point in common variable immunodeficiency
• Expression of IL-17RA in Innate Cells of Patients with Common Variable Immunodeficiency (CVID) and its Clinical Implications
• Follow-up of immune response in patients with common variable immunodeficiency following SARS-CoV-2 vaccination
• Fresh-Frozen Plasma as a Low-Cost Replacement of Intravenous Immunoglobulin for the Treatment of Symptomatic Hypogammaglobulinemia
• Gene Signature of Regulatory T Cells Isolated from Children with Selective IgA Deficiency and Common Variable Immunodeficiency
• Genetic Approaches to Study Rheumatic Diseases and Its Implications in Clinical Practice
• Genetic polymorphisms of TLR1, TLR2, TLR3 and TLR4 in patients with recurrent or severe infections
• Genetics and clinical phenotypes in common variable immunodeficiency
• Granulomatous Lymphocyte Interstitial Lung Disease: A Rare Complication of Common Variable Immunodeficiency Managed With Azathioprine and Rituximab
• Granulomatous Lymphocytic Interstitial Lung Disease Associated With Common Variable Immunodeficiency Presenting With Respiratory Failure
• Heterozygous <em>SERPINA1</em> Defects and Their Impact on Clinical Manifestations of Patients with Predominantly Antibody Deficiencies
• High Prevalence of Long COVID in Common Variable Immunodeficiency: An Italian Multicentric Study
• ICOS agonist vopratelimab modulates follicular helper T cells and improves B cell function in common variable immunodeficiency
• IgD(+)IgM(-) B Cells in Common Variable Immunodeficiency
• Immunogenicity of COVID-19 booster vaccination in IEI patients and their one year clinical follow-up after start of the COVID-19 vaccination program
• Inborn Errors of Immunity in Adults with Autoimmune Liver Diseases
• Inborn Errors of Immunity in Jordan: First Report from a Tertiary Referral Center
• Increased risk of gastric cancer in relation with pernicious anaemia in patients with primary antibody deficiency: A nationwide case control study
• Infection-Related Glomerulonephritis in Children and Adults
• Intermediate uveitis in common variable immunodeficiency (CVID) associated with a heterozygous variant in the TNFRSF13B gene
• Interstitial lung diseases (ILD) in common variable immunodeficiency (CVID) patients: a study from Iran
• IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results
• Limitations in the clinical utility of vaccine challenge responses in the evaluation of primary antibody deficiency including Common Variable Immunodeficiency Disorders
• Multifaceted roles of <em>IKZF1</em> gene, perspectives from bench to bedside
• Nanoparticle delivery of Tat synergizes with classical latency reversal agents to express HIV antigen targets
• Navigating the ethical implications of immunoglobulin replacement therapy during pregnancy
• Noninfectious Complications in B-Lymphopenic Common Variable Immunodeficiency
• Novel hypermorphic variants in IRF2BP2 identified in patients with common variable immunodeficiency and autoimmunity
• Oropharyngeal microbial ecosystem perturbations influence the risk for acute respiratory infections in common variable immunodeficiency
• Pathogenic TNFRSF13B Variant in an Adult Japanese Patient with Common Variable Immunodeficiency
• Possible Role of Cytomegalovirus in Gastric Cancer Development and Recurrent Macrolide-Resistant Campylobacter jejuni Infection in Common Variable Immunodeficiency: A Case Report and Literature Discussion
• Predominantly antibody deficiency and the association with celiac disease in Sweden: A nationwide case-control study
• Proof-of-concept study evaluating humoral primary immunodeficiencies via CJ:KREC ratio and serum BAFF level
• Prophylactic immunoglobulin therapy for pediatric congenital myotonic dystrophy
• Reference values of lymphocyte subsets from healthy Polish adults
• Relationships between bronchiectasis and time to achieving target trough immunoglobulin G levels in patients with common variable immunodeficiency
• Renal complications in patients with predominantly antibody deficiency in the United States Immune Deficiency Network (USIDNET)
• Retraction Note: Rifaximin alters gut microbiota profile, but does not affect systemic inflammation - a randomized controlled trial in common variable immunodeficiency
• Role of B Cells beyond Antibodies in HBV-Induced Oncogenesis: Fulminant Cancer in Common Variable Immunodeficiency-Clinical and Immunotransplant Implications with a Review of the Literature
• Role of Skewed X-Chromosome Inactivation in Common Variable Immunodeficiency
• Sarcoidosis versus Granulomatous and Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency: A Comparative Review
• Sarcoidosis-Lymphoma Syndrome and Common Variable Immunodeficiency Disorder: Finding the Zebra and Overcoming Health Disparity Barriers
• Serum immunoglobulin levels in group E of chronic obstructive pulmonary disease: insights for clinical management and immunoglobulin therapy strategies
• Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine response in adults with predominantly antibody deficiency
• Severe Gastrointestinal Cytomegalovirus Infection in a Patient Diagnosed with Late Onset Combined Immunodeficiency
• Small Bowel Villous Atrophy in a Young Patient: A Challenging Diagnosis
• Systematic review of mortality and survival rates for APDS
• The autoimmune rheumatological presentation of Common Variable Immunodeficiency Disorders with an overview of genetic testing
• The clinical and immunological characteristics of common variable immunodeficiency in adults and older adults
• The common variable immunodeficiency IgM repertoire narrowly recognizes erythrocyte and platelet glycans
• The Etiologic Landscape of Lymphoproliferation in Childhood: Proposal for a Diagnostic Approach Exploring from Infections to Inborn Errors of Immunity and Metabolic Diseases
• The Horse with Recurrent Fevers and Infections: Approach to Common Variable Immunodeficiency
• The Scope and Impact of Viral Infections in Common Variable Immunodeficiency (CVID) and CVID-like Disorders: A Literature Review
• Tolerability and outcomes with rollout of tixagevimab-cilgavimab in patients with common variable immunodeficiency
• Vaccination status of patients with primary immunodeficiencies in Germany-a multicentric epidemiologic analysis
• Variable Expression Common Immune Deficiency: A Report of Five Cases