Scinovex
article Open AccessTop 1% cited

Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients*

British Journal of Dermatology · 2021 · Vol. 186(3) · pp. 564–574
Sophie Georgin‐LavialleBenjamin TerrierAlexis F. GuédonMaël HeibligT. ComontEstibaliz LazaroValentin LacombeLouis TerriouSamuel ArdoisJean‐David BouazizAlexis MathianG. Le GuennoAchille AoubaR. OuthA. MeyerMarielle Roux‐SauvatMikaël EbboLin‐Pierre ZhaoAdrien BigotYvan JamillouxVivien GuillotinEdouard FlamarionPierrick HennetonGuillaume VialVincent JachietJulien RossignolS. VinzioThierry WeittenJ. VinitC. DelignyS. HumbertMaxime SamsonN. Magy‐BertrandT. MoulinetR. BourguibaThomas HanslikClaude BachmeyerMarie SébertMarie KostineBoris BienvenuP. BiscayÉ. LiozonL. SaillerFrançois ChassetAlexandra Audemard‐VergerEugénie DuroyonGuillaume SarrabayFelippe BorlotC. DiévalThomas CluzeauPaola MarianettiHervé LobbesGuilaine BoursierMathieu Gerfaud‐ValentinJuliette JeannelAmélie ServettazSylvain AudiaM. LarueBasile HenriotB. FaucherJ. GraveleauB. De Sainte MarieJoris GallandLaurence BouilletCatherine ArnaudLionel AdèsFabrice CarratPierre HirschPierre FenauxO. FainPierre SujobertOlivier KosmiderA. MékinianFrench VEXAS groupGFEV, GFM, CEREMAIA, MINHEMON

Abstract

VEXAS syndrome has a large spectrum of organ manifestations and shows different clinical and prognostic profiles. It also raises a potential impact of the identified UBA1 mutation.

Otitis Media and Relapsing PolychondritisVascular Anomalies and TreatmentsPeptidase Inhibition and AnalysisMedicineInternal medicineMonoclonal gammopathy of undetermined significanceGastroenterologyImmunologyMonoclonal

MeSH terms

HumansInflammationMonoclonal Gammopathy of Undetermined SignificanceMutationMyelodysplastic SyndromesUbiquitin-Activating Enzymes
Citations
389
FWCI
45.93
field-weighted impact
References
18
Percentile
100%
vs. same field & year
Citations per year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.

Further characterization of clinical and laboratory features in VEXAS syndrome: large‐scale analysis of a multicentre case series of 116 French patients* · Scinovex