Clinical characteristics, disease trajectories and management of vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome: a systematic review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s00296-023-05513-0.pdf
Reference112 articles.
1. Grayson PC, Patel BA, Young NS (2021) VEXAS syndrome. Blood [Internet]. 2021 Jul 1 [cited 2023 Jul 8];137(26):3591–4. https://pubmed.ncbi.nlm.nih.gov/33971000/. Accessed 8 July 2023
2. Beck DB, Ferrada MA, Sikora KA, Ombrello AK, Collins JC, Pei W et al (2020) Somatic mutations in UBA1 and severe adult-onset autoinflammatory disease. N Engl J Med [Internet]. 383(27):2628–2638. https://doi.org/10.1056/NEJMoa2026834
3. Levy-Lahad E, King MC (2020) Hiding in plain sight—somatic mutation in human disease. N Engl J Med [Internet]. 383(27):2680–2682. https://doi.org/10.1056/NEJMe2030754
4. Ruffer N, Krusche M (2023) VEXAS syndrome: a diagnostic puzzle. RMD Open [Internet]. 2023 Aug 1 [cited 2023 Aug 13];9(3):e003332. https://rmdopen.bmj.com/content/9/3/e003332
5. Beck DB, Bodian DL, Shah V, Mirshahi UL, Kim J, Ding Y, et al (2023) Estimated prevalence and clinical manifestations of UBA1 variants associated with VEXAS syndrome in a clinical population. JAMA [Internet]. 2023 Jan 24 [cited 2023 Aug 13];329(4):318–24. https://jamanetwork.com/journals/jama/fullarticle/2800661
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