Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS)-Reference-Cited by-同舟云学术

Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS)

Published:2021-07 Issue: Volume:228 Page:108757
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Tessarin Giulio,Mazza Cinzia,Baronio Manuela,Gazzurelli Luisa,Rossi Stefano,Moratto Daniele,Badolato Raffaele,Rensing-Ehl Anne,Ehl Stephan,Warnatz Klaus,Rosanelli Carlo,Morello Enrico,Plebani Alessandro,Lougaris Vassilios

Funder

Jeffrey Modell Foundation

Ministero dell’Istruzione, dell’Università e della Ricerca

Seventh Framework Programme

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference10 articles.

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4. Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome;Caminha;J. Allergy Clin. Immunol.,2010

5. A composite picture of TcRα/β+ CD4-CD8- T cells (α/β-DNTCs) in humans with autoimmune lymphoproliferative syndrome;Bleesing;Clin. Immunol.,2002

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1. Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children’s Hospital Medical Center;Journal of Clinical Immunology;2024-07-26

2. Autoimmune lymphoproliferative immunodeficiencies (ALPIDs): A proposed approach to redefining ALPS and other lymphoproliferative immune disorders;Journal of Allergy and Clinical Immunology;2024-01

3. 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

4. Presentation and diagnosis of autoimmune lymphoproliferative syndrome (ALPS);Expert Review of Clinical Immunology;2021-09-17