Disease: Severe combined immunodeficiency- X-linked
- <em>In Vivo</em> Gene Therapy for Canine SCID-X1 Using Cocal-Pseudotyped Lentiviral Vector
- A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease
- A great disturbance in the force: IL-2 receptor defects disrupt immune homeostasis
- A Murine Model of X-Linked Moesin-Associated Immunodeficiency (X-MAID) Reveals Defects in T Cell Homeostasis and Migration
- A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers
- An Update on XMEN Disease
- 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
- Break down the barriers of auto-inflammation: How to deal with a monogenic auto-inflammatory disease and immuno-haematological features in 2022?
- Case Report: A Novel IL2RG Frame-Restoring Rescue Mutation Mimics Early T Cell Engraftment Following Haploidentical Hematopoietic Stem Cell Transplantation in a Patient With X-SCID
- Case Report: Interleukin-2 Receptor Common Gamma Chain Defect Presented as a Hyper-IgE Syndrome
- Case report: Novel treatment regimen for <em>enterovirus</em> encephalitis in SCID
- Case Report: PD-1 Inhibitor Is Active in Lung Adenocarcinoma With B Cell Deficiency
- Case report: Persistent shedding of a live vaccine-derived rubella virus in a young man with severe combined immunodeficiency and cutaneous granuloma
- Case Report: X-Linked SASH3 Deficiency Presenting as a Common Variable Immunodeficiency
- Challenges in Gene Therapy for Somatic Reverted Mosaicism in X-Linked Combined Immunodeficiency by CRISPR/Cas9 and Prime Editing
- Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling
- Childhood-onset Takayasu arteritis and immunodeficiency: case-based review
- Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports
- Combined Treatment of Progressive Encephalitis in an X-linked Agammaglobulinemia Patient
- Comparative study of immunodeficient rat strains in engraftment of hiPSC-derived airway epithelia
- Comparative Study of Immunodeficient Rat Strains in Engraftment of Human-Induced Pluripotent Stem Cell-Derived Airway Epithelia
- CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells
- CRISPR-targeted MAGT1 insertion restores XMEN patient hematopoietic stem cells and lymphocytes
- CRISPR/Cas9-mediated gene editing. A promising strategy in hematological disorders
- Current Clinical Applications of In Vivo Gene Therapy with AAVs
- Cutaneous T-cell lymphoma as a unique presenting malignancy in X-linked magnesium defect with EBV infection and neoplasia (XMEN) disease
- Cutaneous vasculitis in autoinflammatory diseases
- Development of human hepatocellular carcinoma in X-linked severe combined immunodeficient pigs: An orthotopic xenograft model
- Early-Onset Inflammatory Bowel Disease Caused by Mutations in the X-Linked Gene IL2RG
- Epigenetic activation of the TUSC3 gene as a potential therapy for XMEN disease
- Epstein-Barr virus-related hemophagocytic lymphohistiocytosis complicated with coronary artery dilation and acute renal injury in a boy with a novel X-linked inhibitor of apoptosis protein (XIAP) variant: a case report
- Exhaustion-like dysfunction of T and NKT cells in an X-linked severe combined immunodeficiency patient with maternal engraftment by single-cell analysis
- Exhaustion‑like dysfunction of T and NKT cells in an X‑linked severe combined immunodeficiency patient with maternal engraftment by single‑cell analysis
- Gene Therapies for Primary Immune Deficiencies
- Gene therapy for X-linked severe combined immunodeficiency: Historical outcomes and current status
- Gene therapy in PIDs, hemoglobin, ocular, neurodegenerative, and hemophilia B disorders
- Generation and characterization of an <em>I</em><em>l2rg</em> knockout Syrian hamster model for XSCID and HAdV-C6 infection in immunocompromised patients
- Generation of knockout rabbits with X-linked severe combined immunodeficiency (X-SCID) using CRISPR/Cas9
- Haematopoietic Stem Cell Transplantation (HSCT) for Primary Immune System Disorders in Children: A Single Centre Experience
- Haploidentical Hematopoietic Stem Cell Transplantation for XIAP Deficiency: a Single-Center Report
- Health-Related Quality of Life in 91 Patients with X-Linked Agammaglobulinemia
- Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases
- Hemophagocytic syndrome associated with Mycobacterium bovis in a patient with X-SCID: a case report
- Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease
- Immune Reconstitution After Gene Therapy Approaches in Patients With X-Linked Severe Combined Immunodeficiency Disease
- Immune Responses 6 Months After mRNA-1273 COVID-19 Vaccination and the Effect of a Third Vaccination in Patients with Inborn Errors of Immunity
- Immunodeficiency
- Immunodeficiency
- Immunogenicity of the mRNA-1273 COVID-19 vaccine in adult patients with inborn errors of immunity
- Inborn errors of immunity and related microbiome
- Inborn Errors of Immunity-the Sri Lankan Experience 2010-2022
- Infectious Complications Predict Premature CD8<sup>+</sup> T-cell Senescence in CD40 Ligand-Deficient Patients
- Initial manifestations in Patients with Inborn Errors of Immunity Based on Onset Age: a Study from a Nationwide Survey in Japan
- Integrome signatures of lentiviral gene therapy for SCID-X1 patients
- Interstitial pneumonia as the initial presentation in an infant with a novel mutation of CD40 ligand-associated X-linked hyper-IgM syndrome: A case report
- Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation
- Laryngeal Cartilage Regeneration of Nude Rats by Transplantation of Mesenchymal Stem Cells Derived from Human-Induced Pluripotent Stem Cells
- Lentivector cryptic splicing mediates increase in CD34+ clones expressing truncated HMGA2 in human X-linked severe combined immunodeficiency
- Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development
- Lymphoproliferative Disorders
- Lymphoproliferative Disorders
- Lymphoproliferative disorders and inborn errors of immunity
- Magnesium in Infectious Diseases in Older People
- Microbiome and Its Dysbiosis in Inborn Errors of Immunity
- Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years
- Newborn screening for severe combined immunodeficiency: The results of the first pilot TREC and KREC study in Ukraine with involving of 10,350 neonates
- Next generation sequencing analysis of consecutive Russian patients with clinical suspicion of inborn errors of immunity
- Non-viral <em>ex vivo</em> genome-editing in mouse bona fide hematopoietic stem cells with CRISPR/Cas9
- Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome
- Peripheral B Cell Deficiency and Predisposition to Viral Infections: The Paradigm of Immune Deficiencies
- Pneumocystis jirovecii and SARS-CoV-2 Coinfection as Presentation of X-linked Severe Combined Immunodeficiency
- Preclinical Development of Autologous Hematopoietic Stem Cell-Based Gene Therapy for Immune Deficiencies: A Journey from Mouse Cage to Bed Side
- Prime Editing for Human Gene Therapy: Where Are We Now?
- Progressive B Cell Loss in Revertant X-SCID
- Pulmonary Radiological Manifestations of Humoral and Combined Immunodeficiencies in a Tertiary Pediatric Center
- Reactogenicity and immunogenicity of the second COVID-19 vaccination in patients with inborn errors of immunity or mannan-binding lectin deficiency
- 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
- RIOK3-Mediated Akt phosphorylation facilitates synergistic replication of Marek's disease and reticuloendotheliosis viruses
- SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation
- Scales of Magt1 Gene: Novel Mutations, Different Presentations
- Severe Combined Immunodeficiency (SCID) and Its New Treatment Modalities
- Severe Combined Immunodeficiency-Classification, Microbiology Association and Treatment
- Severe Fatigue Is Common Among Pediatric Patients with Primary Immunodeficiency and Is Not Related to Disease Activity
- Severity of SARS-CoV-2 infection in children with inborn errors of immunity (primary immunodeficiencies): a systematic review
- Somatic Reversion of a Novel <em>IL2RG</em> Mutation Resulting in Atypical X-Linked Combined Immunodeficiency
- Somatic Reversion of a Novel IL2RG Mutation Resulting in Atypical X-Linked Combined Immunodeficiency
- Successful living donor liver transplantation for liver failure due to maternal T cell engraftment following cord blood transplantation in X-linked severe combined immunodeficiency disease: Case report
- Successful SCID gene therapy in infant with disseminated BCG
- Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity
- The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases
- Transplantation of human cells into Interleukin-2 receptor gamma gene knockout pigs under several conditions
- Utility of targeted next generation sequencing for inborn errors of immunity at a tertiary care centre in North India
- Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon
- X-Linked Immunodeficiency
- X-Linked Immunodeficiency
- X-linked immunodeficient (XID) mice exhibit high susceptibility to Cryptococcus gattii infection
- X-Linked Immunodeficient Mice With No Functional Bruton's Tyrosine Kinase Are Protected From Sepsis-Induced Multiple Organ Failure
- X-linked SCID with a rare mutation
- X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia