• 14-3-3eta Proteins as a Diagnostic Marker, Disease Activation Indicator, and Lymphoma Predictor in Patients with Primary Sjogren Syndrome
• 14-3-3η Proteins as a Diagnostic Marker, Disease Activation Indicator, and Lymphoma Predictor in Patients with Primary Sjögren Syndrome
• A case of autoimmune lymphoproliferative syndrome with a novel <em>de novo FAS</em> variant
• A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant
• A case of cold agglutinin syndrome associated with chronic lymphocytic leukaemia harbouring mutations in CARD11 and KMT2D
• A Challenging Case of Adult-Onset Still's Disease Complicated by Macrophage Activation Syndrome With Multiorgan Failure
• A rare immunological disease, caspase 8 deficiency: case report and literature review
• Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing
• Acquired von Willebrand syndrome (AvWS)
• Acquired von willebrand syndrome secondary to monoclonal gammopathy of undetermined significance: long-term remission after treatment with bortezomib
• Activated phosphoinositide 3-kinase delta syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
• Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
• Anti-Glycolipid Antibody Examination in Five EAE Models and Theiler's Virus Model of Multiple Sclerosis: Detection of Anti-GM1, GM3, GM4, and Sulfatide Antibodies in Relapsing-Remitting EAE
• Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation
• Autoimmune lymphoproliferative immunodeficiencies (ALPIDs): A proposed approach to redefining ALPS and other lymphoproliferative immune disorders
• Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?
• Autoimmune lymphoproliferative syndrome (ALPS) due to a novel dominant negative germline mutation in the FAS gene
• Autoimmune lymphoproliferative syndrome identified through reverse phenotyping
• Autoimmune lymphoproliferative syndrome: a case report
• Autoimmune lymphoproliferative syndrome: A disorder of immune dysregulation
• Autoimmune-lymphoproliferative immunodeficiencies (ALPID) A proposed approach to redefining ALPS and other lymphoproliferative immune disorders
• Bilateral Panuveitis in an Adolescent with Autoimmune Lymphoproliferative Syndrome Due to CTLA4 Haploinsufficiency
• Case report: Effectiveness of sirolimus in treating partial DiGeorge Syndrome with Autoimmune Lymphoproliferative Syndrome (ALPS)-like features
• Case report: Neonatal autoimmune lymphoproliferative syndrome with a novel pathogenic homozygous <em>FAS</em> variant effectively treated with sirolimus
• Case report: Neonatal autoimmune lymphoproliferative syndrome with a novel pathogenic homozygous FAS variant effectively treated with sirolimus
• Case report: Synergistic defects of CASP10 and BTK leading to autoimmune lymphoproliferative syndrome type IIa, complicated by severe hemophagocytic lymphohistiocytosis
• Castleman disease and mimickers: Clinicopathological findings of atypical lymphoproliferative disorders associated with autoimmune disease
• Chai Disease Mimicking Autoimmune Lymphoproliferative Syndrome
• Characterizing the regulatory Fas (CD95) epitope critical for agonist antibody targeting and CAR-T bystander function in ovarian cancer
• Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity
• Clinical Presentation of Schnitzler's Syndrome: A Rare Autoimmune Disease
• Clinical, immunologic, and genetic characteristics of children with ALPS: A single-center experience
• Collage of cases and brief review of the laboratory diagnosis and molecular testing in autoimmune haemolytic anaemia
• Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
• Comparative analysis of the development mechanisms of cryoglobulinemic vasculitis and Sjogren's syndrome
• Complement-directed therapy for cold agglutinin disease: sutimlimab
• Complete miRNA-15/16 loss in mice promotes hematopoietic progenitor expansion and a myeloid-biased hyperproliferative state
• Cryoglobulinemia
• Cryoglobulinemia
• Cutaneous Eruption Associated with Sirolimus in a Child with FAS-Associated Autoimmune Lymphoproliferative Syndrome
• Detection and evolutionary dynamics of somatic FAS variants in autoimmune lymphoproliferative syndrome: Diagnostic implications
• Detection of signature double-negative T cells is a predictive marker to identify autoimmune lymphoproliferative syndrome associated with FAS loss of function
• Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study
• Double-Negative T (DNT) Cells in Patients with Systemic Lupus Erythematosus
• Ecodatacube.eu: analysis-ready open environmental data cube for Europe
• Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
• Eosinophilic gastrointestinal disorders in patients with inborn errors of immunity: Data from the USIDNET registry
• Evans Syndrome
• Evans Syndrome
• Evans syndrome in a young man with rare autoimmune associations and transplanted liver
• Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas-mediated apoptotic pathway
• Guardians of Immunity: Advances in Primary Immunodeficiency Disorders and Management
• Hypogammaglobulinemia and immune dysregulation - not just two sides of a coin
• Hypogammaglobulinemia and immune dysregulation-not just 2 sides of a coin
• Inborn errors of immunity and related microbiome
• Infections in Disorders of Immune Regulation
• Large granular lymphocytic leukemia and its association with immune dysregulation
• Late-Onset Autoimmune Lymphoproliferative Syndrome in a Costa Rican Woman
• Lymphoproliferative Disorders
• Lymphoproliferative Disorders
• Mixed Warm and Cold Autoimmune Hemolytic Anemia With Concomitant Immune Thrombocytopenia Following Recent SARS-CoV-2 Infection and Ongoing Rhinovirus Infection
• Monoallelic KRAS (G13C) mutation triggers dysregulated expansion in induced pluripotent stem cell-derived hematopoietic progenitor cells
• Naproxen-Induced Evans Syndrome
• Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
• Nonbacterial thrombotic endocarditis of mitral valve associated with a lymphoproliferative malignancy: case report and literature review
• Novel Germline TET2 Mutations in Two Unrelated Patients with Autoimmune Lymphoproliferative Syndrome-Like Phenotype and Hematologic Malignancy
• Opinion paper: effectiveness of sirolimus in treating partial Di George syndrome with autoimmune lymphoproliferative syndrome-like features
• P2X7 purinergic receptor plays a critical role in maintaining T-cell homeostasis and preventing lupus pathogenesis
• Paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome: Part I. clinical overview and pathophysiology
• Phenotypic Variability in PRKCD: a Review of the Literature
• Presentation of Sjogren Syndrome as Nodular Pulmonary Amyloidosis
• Primary Sjogren's syndrome misdiagnosed as Mikulicz's disease: a case report
• Probable Autoimmune Lymphoproliferative Syndrome with Monogenic Lupus Due to KRAS Mutation
• Progressive multifocal leukoencephalopathy in anti-CD20 and other monoclonal antibody (mAb) therapies used in multiple sclerosis: A review
• Rare diseases presenting with hemophagocytic lymphohistiocytosis
• Refractory immune thrombocytopenia: Lessons from immune dysregulation disorders
• Regulatory T-cell deficiency leads to features of autoimmune liver disease overlap syndrome in scurfy mice
• Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
• Role for Caspase-8 in the Release of IL-1β and Active Caspase-1 from Viable Human Monocytes during Toxoplasma gondii Infection
• Rosai-Dorfman Disease between Proliferation and Neoplasia
• S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV)
• Severe autoimmune lymphoproliferative syndrome phenotype in a pediatric patient with a germline FAS gene variant
• Severe RAS-Associated Lymphoproliferative Disease Case with Increasing alphabeta Double-Negative T Cells with Atypical Features
• Severe RAS-Associated Lymphoproliferative Disease Case with Increasing αβ Double-Negative T Cells with Atypical Features
• Skin Manifestations in Patients with Selective Immunoglobulin E Deficiency
• Skin-Limited, Methotrexate-Associated Epstein-Barr Virus-Positive Mucocutaneous Ulcer-A Mimicker of High-Grade Lymphoma. A Report of 4 Cases and Review of the Literature
• Sonographic Appearance of Lacrimal Glands in Sjogren's Syndrome at High Risk for Lymphoma Development
• STAT3 gain-of-function syndrome
• Summer rain and wet soil rather than management affect the distribution of a toxic plant in production grasslands
• TAFRO Syndrome: A Syndrome or a Subtype of Multicentric Castleman Disease?
• The decreased of peripheral blood natural killer cell is associated with serum IL-2 level in the renal tubular acidosis in patients with primary sjogren's syndrome
• The impact of Treosulfan-based conditioning for inborn errors of immunity: Is dose monitoring crucial?
• The role of caspase-8 in inflammatory signalling and pyroptotic cell death
• Therapeutic Options in Refractory Evans Syndrome: A Case Report
• Understanding the Spectrum of Immune Dysregulation Manifestations in Autoimmune Lymphoproliferative Syndrome and Autoimmune Lymphoproliferative Syndrome-like Disorders
• Unusual Polyclonal IgM in an IgG Deficient Patient with Autoimmune Lymphoproliferative Syndrome: A Case Study and Literature Review
• Unveiling the Uncommon: A Unique Case of ALPS-Like Syndrome Complicated by Plasma Cell Disorder
• Validation of Artificial Intelligence (AI)-Assisted Flow Cytometry Analysis for Immunological Disorders
• Various phenotypes of <em>LRBA</em> gene with compound heterozygous variation: A case series report of pediatric cytopenia patients
• Wiskott-Aldrich syndrome protein interacts and inhibits diacylglycerol kinase alpha promoting IL-2 induction