Thrombosis in VEXAS syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Hematology
Link
https://link.springer.com/content/pdf/10.1007/s11239-021-02608-y.pdf
Reference20 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(27):2628–2638. https://doi.org/10.1056/NEJMoa20268342
2. Fan BE, Cao L, Gallardo CA et al (2021) Myeloid and lymphoid vacuolation in VEXAS syndrome. Am J Hematol 96(8):1056–1057. https://doi.org/10.1002/ajh.26098
3. Georgin-Lavialle S, Terrier B, Guedon AF et al (2021) Further characterization of clinical and laboratory features occurring in VEXAS syndrome in a large-scale analysis of multicenter case-series of 116 French patients. Br J Dermatol. https://doi.org/10.1111/bjd.20805
4. Obiorah IE, Patel BA, Groarke EM et al (2021) Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1. Blood Adv 5(16):3203–3215. https://doi.org/10.1182/bloodadvances.2021004976
5. van der Made CI, Potjewijd J, Hoogstins A et al (2021) Adult-onset autoinflammation caused by somatic mutations in UBA1: a Dutch case series of patients with VEXAS. J Allergy Clin Immunol. https://doi.org/10.1016/j.jaci.2021.05.014
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