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Quoted phrase not found in phrase index: "Chronic noninfectious lymphadenopathy"
Page 1
Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes.
Biomed J. 2021 Aug;44(4):400-411. doi: 10.1016/j.bj.2021.04.005. Epub 2021 Apr 19.
Biomed J. 2021.
PMID: 34384744
Free PMC article.
Review.
The resulting FAS-mediated apoptosis defect accounts for the expansion and accumulation of autoreactive (double-negative) T cells leading to cytopenias, splenomegaly, lymphadenopathy, autoimmune disorders, and risk of lymphoma. However, there are other monogenetic disorder …
The resulting FAS-mediated apoptosis defect accounts for the expansion and accumulation of autoreactive (double-negative) T cells leading to …
The Clinical and Immunological Features of Patients with Primary Antibody Deficiencies.
Azizi G, Bagheri Y, Tavakol M, Askarimoghaddam F, Porrostami K, Rafiemanesh H, Yazdani R, Kiaee F, Habibi S, Abouhamzeh K, Mohammadi H, Qorbani M, Abolhassani H, Aghamohammadi A.
Azizi G, et al.
Endocr Metab Immune Disord Drug Targets. 2018;18(5):537-545. doi: 10.2174/1871530318666180413110216.
Endocr Metab Immune Disord Drug Targets. 2018.
PMID: 29651973
Among the noninfectious complications, autoimmunity (26.2%), and splenomegaly (23.4%) were the most common. Lymphadenopathy was higher in CSD patients than other PADs, while splenomegaly, hepatomegaly, autoimmunity and bronchiectasis were more common in CVID patient …
Among the noninfectious complications, autoimmunity (26.2%), and splenomegaly (23.4%) were the most common. Lymphadenopathy wa …
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