Disease: Bare lymphocyte syndrome
- <em>Dclre1c</em>-Mutation-Induced Immunocompromised Mice Are a Novel Model for Human Xenograft Research
- A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID
- A large single-center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey
- A new neonatal BCG vaccination pathway in England: a mixed methods evaluation of its implementation
- A novel 268 kb deletion combined with a splicing variant in IL7R causes of severe combined immunodeficiency in a Chinese family: a case report
- A novel, small anti-HBV compound reduces HBsAg and HBV-DNA by destabilizing HBV-RNA
- A Reappraisal of the Antiviral Properties of and Immune Regulation through Dietary Phytochemicals
- A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report
- An Antiherpesviral Host-Directed Strategy Based on CDK7 Covalently Binding Drugs: Target-Selective, Picomolar-Dose, Cross-Virus Reactivity
- Analysis of efficacy and prognosis of allogeneic hematopoietic stem cell transplantation for the treatment of combined immunodeficiency
- Ang1/Tie2/VE-Cadherin Signaling Regulates DPSCs in Vascular Maturation
- Assistance of next-generation sequencing for diagnosis of disseminated Bacillus Calmette-Guerin disease with X-SCID in an infant: a case report and literature review
- BCL10 Deficiency Presenting as Severe Combined Immunodeficiency Escaping Newborn Screening
- Bright ferritin for long-term MR imaging of human embryonic stem cells
- Case Report: Profound newborn leukopenia related to a novel RAC2 variant
- Case report: Refractory Evans syndrome in two patients with spondyloenchondrodysplasia with immune dysregulation treated successfully with JAK1/JAK2 inhibition
- Case Report: The impact of severe cryptosporidiosis on the gut microbiota of a pediatric patient with CD40L immunodeficiency
- Characterization of Human Engraftment and Hemophagocytic Lymphohistiocytosis in NSG-SGM3 Neonate Mice Engrafted with Purified CD34<sup>+</sup> Hematopoietic Stem Cells
- Clinical and functional spectrum of RAC2-related immunodeficiency
- Clinical heterogeneity in families with multiple cases of inborn errors of immunity
- Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report
- Complement C1s deficiency in a male Caucasian patient with systemic lupus erythematosus: a case report
- COVID-19, HIV, and Cryptococcal Meningitis Coinfections with Abnormal Laboratory Findings
- CRISPR/Cas9-Based Disease Modeling and Functional Correction of Interleukin 7 Receptor Alpha Severe Combined Immunodeficiency in T-Lymphocytes and Hematopoietic Stem Cells
- CRISPR/Cas9-based disease modelling and functional correction of Interleukin 7 Receptor alpha Severe Combined Immunodeficiency in T-lymphocytes and hematopoietic stem cells
- Cutaneous vasculitis in autoinflammatory diseases
- CXCR4 WHIM syndrome is a cancer predisposition condition for virus-induced malignancies
- Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette-Guerin in Iranian children
- Development of a HPLC-MS/MS Method to Assess the Pharmacokinetics and Tumour Distribution of the Dimethylarginine Dimethylaminohydrolase 1 Inhibitors ZST316 and L-257 in a Xenograft Model of Triple-Negative Breast Cancer in Mice
- Development of chimeric antigen receptor (CAR)-T cells targeting A56 viral protein implanted by oncolytic virus
- Differential Diagnosis: Hepatic Complications in Inborn Errors of Immunity
- DiGeorge Syndrome
- Disseminated tuberculosis complicating Bacillus Calmette-Guerin (BCG) vaccine as only presentation of severe combined immunodeficiency (SCID): A report of 3 cases
- Effect of Cell Density of a Methacrylic Acid-Based Hydrogel Implant on Embedded Islet Function and Viability
- EXPANDED NEWBORN SCREENING FOR INBORN ERRORS OF IMMUNITY: THE EXPERIENCE OF TUSCANY
- Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit beta-type 10 in six infants with SCID-Omenn syndrome
- From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature
- Gene therapy for adenosine deaminase severe combined immune deficiency-An unexpected journey of four decades
- Genetically corrected RAG2-SCID human hematopoietic stem cells restore V(D)J-recombinase and rescue lymphoid deficiency
- Granulomas in Pediatric Liver Biopsies: Single Center Experience
- HIV and COVID-19: two pandemics with significant (but different) central nervous system complications
- Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome
- IMiD/CELMoD-induced growth suppression of adult T-cell leukemia/lymphoma cells <em>via</em> cereblon through downregulation of target proteins and their downstream effectors
- Inborn Errors of Immunity in Jordan: First Report from a Tertiary Referral Center
- Increased mortality in infants with abnormal T-cell receptor excision circles
- Infliximab as successful treatment option in a case of adenosine deaminase 2 deficiency
- Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency
- Lymphoproliferative Disorders
- Mechanisms of action of an investigational new freeze-dried platelet-derived hemostatic product
- Meconium peritonitis in multiple intestinal atresia with combined immune deficiency caused by a <em>TTC7A</em> mutation: A case report
- Meconium peritonitis in multiple intestinal atresia with combined immune deficiency caused by a TTC7A mutation: A case report
- Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years
- Mutational analysis in different genes underlying severe combined immunodeficiency in seven consanguineous Pakistani families
- Newborn Screening for Severe Combined Immunodeficiency: Lessons Learned from Screening and Follow-Up of the Preterm Newborn Population
- Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns
- Newborn Screening Today and Tomorrow: A Brief Report from the International Primary Immunodeficiencies Congress
- Non-conditioned cord blood transplantation for infection control in athymic CHARGE syndrome
- Novel Compound Heterozygous ZAP70 R37G A507T Mutations in Infant with Severe Immunodeficiency
- Novel Presentation of Major Histocompatibility Complex Class II Deficiency with Hemophagocytic Lymphohistiocytosis
- Novel Synonymous Variant in IL7R Causes Preferential Expression of the Soluble Isoform
- Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3
- Ovarian cancer cells regulate their mitochondrial content and high mitochondrial content is associated with a poor prognosis
- Parental Engagement in Identifying Information Needs After Newborn Screening for Families of Infants with Suspected Athymia
- Partial correction of immunodeficiency by lentiviral vector gene therapy in mouse models carrying Rag1 hypomorphic mutations
- PAX1 represses canonical Wnt signaling pathway and plays dual roles during endoderm differentiation
- Periodontal disease in patients with WHIM syndrome
- Pharmacokinetic of ceftazidime-avibactam in a critically ill patient under high-volume continuous venovenous haemodiafiltration: A first paediatric case report
- Pharmacokinetic of Ceftazidime-Avibactam in a critically ill patient under high-volume continuous venovenous hemodiafiltration : a first pediatric case report
- Phenotypic spectrum in a family with a novel <em>RAC2</em> p.I21S dominant-activating mutation
- Primary and secondary defects of the thymus
- Proposal for a Disease Activity Score and Disease Damage Score for ADA2 Deficiency: the DADA2AI and DADA2DI
- Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion
- Rapid Diagnosis of Hemophagocytic Lymphohistiocytosis Triggered by Disseminated BCG Infection in Infants With Severe Combined Immunodeficiency: Case Report
- Rare and severe adverse events in children with inflammatory bowel disease: analysis of data from the PIBD-SETQuality Safety Registry
- Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis
- Reducing Mortality and Morbidity in Children with Severe Combined Immunodeficiency in Switzerland: the Role of Newborn Screening
- Relevance of lymphocyte proliferation to PHA in severe combined immunodeficiency (SCID) and T cell lymphopenia
- Respiratory syncytial virus subtypes in children with bronchiolitis: does it correlate with clinical severity?
- Restoration of T and B cell generation in X-linked severe combined immunodeficiency mice through adenine base editing of hematopoietic stem cells
- Restoring T and B cell generation in X-linked severe combined immunodeficiency mice through hematopoietic stem cells adenine base editing
- Rhizopus microsporus and Mucor racemosus coinfection following COVID-19 detected by metagenomics next-generation sequencing: A case of disseminated mucormycosis
- Secondary bone marrow graft loss after third-party virus-specific T cell infusion: Case report of a rare complication
- Severe Combined Immunodeficiency
- Severe Combined Immunodeficiency (SCID) and Its New Treatment Modalities
- Severe combined immunodeficiency diagnosis and genetic defects
- Shorter birth length and decreased T-cell production and function predict severe infections in children with non-severe combined immunodeficiency cartilage-hair hypoplasia
- Stem Cell Transplant in Immune-deficiency-associated Vaccine-derived Poliovirus
- Successful management of delayed-onset adenosine deaminase deficiency with novel mutation
- Survival After Hematopoietic Stem Cell Transplantation in Severe Combined Immunodeficiency (SCID): A Worldwide Review of the Prognostic Variables
- The New Frontiers of Gene Therapy and Gene Editing in Inflammatory Diseases
- The Tumor Growth Inhibitory Effect of a Standardized Extract of Cultured Lentinula edodes Mycelia Using Patient Derived Xenograft Model
- Therapeutic effects of in vivo administration of an inhibitor of tryptophan 2,3-dioxygenase (680c91) for the treatment of fibroids: a preclinical study
- Thymoma with immunodeficiency, combined diffuse panbronchiolitis, and latent autoimmune diabetes in adults- case report and systematic review
- Treatment of plaque-psoriasis in HIV-positive patients
- Treatment with Elapegademase Restores Immunity in Infants with Adenosine Deaminase Deficient Severe Combined Immunodeficiency
- Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis
- Unraveling the Natural History of Good's Syndrome: A Progressive Adult Combined Immunodeficiency
- Unraveling the natural history of Good's Syndrome: A progressive combined adult immunodeficiency
- Validation of nuclear receptor RORγ isoform 1 as a novel host-directed antiviral target based on the modulation of cholesterol levels
- Whole-exome sequencing to identify undiagnosed primary immunodeficiency disorders in children with community-acquired sepsis, admitted in the pediatric intensive care unit