UBA1 gene mutation in giant cell arteritis
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s10067-021-06022-w.pdf
Reference7 articles.
1. Beck DB, Ferrada MA, Sikora KA et al (2020) Somatic mutations in UBA1 and severe adult-onset autoinflammatory disease. N Engl J Med 383:2628–2638. https://doi.org/10.1056/nejmoa2026834
2. Onuora S (2021) Somatic mutations cause VEXAS syndrome. Nat Rev Rheumatol 17:2026834. https://doi.org/10.1038/s41584-020-00559-x
3. Fan BE, Cao L, Gallardo CA, et al (2021) Myeloid and lymphoid vacuolation in VEXAS syndrome. Am J Hematol. https://doi.org/10.1002/ajh.26098
4. Weyand CM, Goronzy JJ (2013) Immune mechanisms in medium and large-vessel vasculitis. Nat Rev Rheumatol 9:731–740. https://doi.org/10.1038/nrrheum.2013.161
5. Arlet J-B, Terrier B, Kosmider O (2021) Mutant UBA1 and severe adult-onset autoinflammatory disease. N Engl J Med 384:2163. https://doi.org/10.1056/NEJMc2102124
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2. Clonal haematopoiesis and UBA1 mutations in individuals with biopsy-proven giant cell arteritis and population-based controls;Rheumatology;2023-08-26
3. Makrozytäre Anämie und Polychondritis: VEXAS-Syndrom;Zeitschrift für Rheumatologie;2023-02-03
4. Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome presenting as recurrent aseptic peritonitis in a patient receiving peritoneal dialysis: a case report;2023-01-11
5. An update on VEXAS syndrome;Expert Review of Clinical Immunology;2022-12-26
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