Autoimmune lymphoproliferative syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Immunology,Immunology and Allergy
Reference56 articles.
1. Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity
2. Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome
3. Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency
4. Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II
5. Chronic lymphadenopathy simulating malignant lymphoma
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1. A rare immunological disease, caspase 8 deficiency: case report and literature review;Allergy, Asthma & Clinical Immunology;2023-04-10
2. 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 Immunology;2022-12
3. Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS);Clinical Immunology;2021-07
4. Neonatal Autoimmune Lymphoproliferative Syndrome: A Case Report and A Brief Review;Journal of Pediatric Hematology/Oncology;2020-03-06
5. Dual Role of Fas/FasL-Mediated Signal in Peripheral Immune Tolerance;Frontiers in Immunology;2017-04-05
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