These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
463 related articles for article (PubMed ID: 35126364)
1. Case Report: Genetic Double Strike: VEXAS and TET2-Positive Myelodysplastic Syndrome in a Patient With Long-Standing Refractory Autoinflammatory Disease. Lötscher F; Seitz L; Simeunovic H; Sarbu AC; Porret NA; Feldmeyer L; Borradori L; Bonadies N; Maurer B Front Immunol; 2021; 12():800149. PubMed ID: 35126364 [TBL] [Abstract][Full Text] [Related]
2. Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS. van der Made CI; Potjewijd J; Hoogstins A; Willems HPJ; Kwakernaak AJ; de Sevaux RGL; van Daele PLA; Simons A; Heijstek M; Beck DB; Netea MG; van Paassen P; Elizabeth Hak A; van der Veken LT; van Gijn ME; Hoischen A; van de Veerdonk FL; Leavis HL; Rutgers A J Allergy Clin Immunol; 2022 Jan; 149(1):432-439.e4. PubMed ID: 34048852 [TBL] [Abstract][Full Text] [Related]
4. Clinical characteristics, disease trajectories and management of vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome: a systematic review. Kouranloo K; Dey M; Almutawa J; Myall N; Nune A Rheumatol Int; 2024 Jul; 44(7):1219-1232. PubMed ID: 38129348 [TBL] [Abstract][Full Text] [Related]
5. Characteristic bone marrow findings in patients with UBA1 somatic mutations and VEXAS syndrome. Patel N; Dulau-Florea A; Calvo KR Semin Hematol; 2021 Oct; 58(4):204-211. PubMed ID: 34802541 [TBL] [Abstract][Full Text] [Related]
6. Clinical Heterogeneity of the VEXAS Syndrome: A Case Series. Koster MJ; Kourelis T; Reichard KK; Kermani TA; Beck DB; Cardona DO; Samec MJ; Mangaonkar AA; Begna KH; Hook CC; Oliveira JL; Nasr SH; Tiong BK; Patnaik MM; Burke MM; Michet CJ; Warrington KJ Mayo Clin Proc; 2021 Oct; 96(10):2653-2659. PubMed ID: 34489099 [TBL] [Abstract][Full Text] [Related]
7. Vacuoles in neutrophil precursors in VEXAS syndrome: diagnostic performances and threshold. Lacombe V; Prevost M; Bouvier A; Thépot S; Chabrun F; Kosmider O; Lacout C; Beucher A; Lavigne C; Geneviève F; Urbanski G Br J Haematol; 2021 Oct; 195(2):286-289. PubMed ID: 34340250 [No Abstract] [Full Text] [Related]
8. UBA1 and DNMT3A mutations in VEXAS syndrome. A case report and literature review. Shaukat F; Hart M; Burns T; Bansal P Mod Rheumatol Case Rep; 2022 Jan; 6(1):134-139. PubMed ID: 34480172 [TBL] [Abstract][Full Text] [Related]
9. VEXAS syndrome: An update. Khitri MY; Hadjadj J; Mekinian A; Jachiet V Joint Bone Spine; 2024 Jul; 91(4):105700. PubMed ID: 38307404 [TBL] [Abstract][Full Text] [Related]
10. VEXAS syndrome in a woman. Barba T; Jamilloux Y; Durel CA; Bourbon E; Mestrallet F; Sujobert P; Hot A Rheumatology (Oxford); 2021 Nov; 60(11):e402-e403. PubMed ID: 33930131 [No Abstract] [Full Text] [Related]
11. [Clinical and genetic features of MDS associated with VEXAS syndrome]. Kunimoto H Rinsho Ketsueki; 2024; 65(4):255-264. PubMed ID: 38684436 [TBL] [Abstract][Full Text] [Related]
12. Comprehensive morphologic characterization of bone marrow biopsy findings in a large cohort of patients with VEXAS syndrome: A single-institution longitudinal study of 111 bone marrow samples from 52 patients. Olteanu H; Patnaik M; Koster MJ; Herrick JL; Chen D; He R; Viswanatha D; Warrington KJ; Go RS; Mangaonkar AA; Kourelis T; Hines A; Gibson SE; Peterson JF; Reichard KK Am J Clin Pathol; 2024 Jun; 161(6):609-624. PubMed ID: 38413044 [TBL] [Abstract][Full Text] [Related]
13. Ocular and orbital manifestations in VEXAS syndrome. Abumanhal M; Leibovitch I; Zisapel M; Eviatar T; Edel Y; Ben Cnaan R Eye (Lond); 2024 Jun; 38(9):1748-1754. PubMed ID: 38548942 [TBL] [Abstract][Full Text] [Related]
14. The heterogeneity of lung involvement in vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome: a case of hypersensitivity pneumonitis-like pattern. Iannone C; Pellico MR; Campochiaro C; Tescaro L; Zompatori M; Caminati A; Harari S; Caporali R Reumatismo; 2024 Jun; 76(2):. PubMed ID: 38916169 [TBL] [Abstract][Full Text] [Related]
15. Somatic Mutations in Beck DB; Ferrada MA; Sikora KA; Ombrello AK; Collins JC; Pei W; Balanda N; Ross DL; Ospina Cardona D; Wu Z; Patel B; Manthiram K; Groarke EM; Gutierrez-Rodrigues F; Hoffmann P; Rosenzweig S; Nakabo S; Dillon LW; Hourigan CS; Tsai WL; Gupta S; Carmona-Rivera C; Asmar AJ; Xu L; Oda H; Goodspeed W; Barron KS; Nehrebecky M; Jones A; Laird RS; Deuitch N; Rowczenio D; Rominger E; Wells KV; Lee CR; Wang W; Trick M; Mullikin J; Wigerblad G; Brooks S; Dell'Orso S; Deng Z; Chae JJ; Dulau-Florea A; Malicdan MCV; Novacic D; Colbert RA; Kaplan MJ; Gadina M; Savic S; Lachmann HJ; Abu-Asab M; Solomon BD; Retterer K; Gahl WA; Burgess SM; Aksentijevich I; Young NS; Calvo KR; Werner A; Kastner DL; Grayson PC N Engl J Med; 2020 Dec; 383(27):2628-2638. PubMed ID: 33108101 [TBL] [Abstract][Full Text] [Related]
16. Clinical and genetic features of Japanese cases of MDS associated with VEXAS syndrome. Kunimoto H; Miura A; Maeda A; Tsuchida N; Uchiyama Y; Kunishita Y; Nakajima Y; Takase-Minegishi K; Yoshimi R; Miyazaki T; Hagihara M; Yamazaki E; Kirino Y; Matsumoto N; Nakajima H Int J Hematol; 2023 Oct; 118(4):494-502. PubMed ID: 37062784 [TBL] [Abstract][Full Text] [Related]
17. Recurrent orbital inflammation associated with VEXAS syndrome. Beecher MB; Tong JY; Halliday LA; Hissaria P; Selva D Orbit; 2024 Jun; 43(3):350-353. PubMed ID: 36168114 [TBL] [Abstract][Full Text] [Related]