Yvan Jamilloux
Overview
Explore the profile of Yvan Jamilloux including associated specialties, affiliations and a list of published articles.
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131
Citations
2135
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Recent Articles
1.
Martin A, Caron S, Marcotte M, Bronnec P, Garneret E, Martel N, et al.
iScience
. 2025 Jan;
28(1):111563.
PMID: 39868044
Alpha-kinase 1 (ALPK1) is an immune receptor sensing the bacterial nucleotide sugar ADP-heptose. ALPK1 phosphorylates TIFA leading to its oligomerization and downstream NF-κB activation. Specific mutations in are associated with...
2.
Jacquot R, Ren L, Wang T, Mellahk I, Duclos A, Kodjikian L, et al.
Eye (Lond)
. 2024 Dec;
PMID: 39706896
Background/objectives: The large number and heterogeneity of causes of uveitis make the etiological diagnosis a complex task. The clinician must consider all the information concerning the ophthalmological and extra-ophthalmological features...
3.
Fautrel B, Mitrovic S, De Matteis A, Bindoli S, Anton J, Belot A, et al.
Ann Rheum Dis
. 2024 Sep;
83(12):1614-1627.
PMID: 39317417
Methods: In May 2022, EULAR and PReS endorsed a proposal for a joint task force (TF) to develop recommendations for the diagnosis and management of sJIA and AOSD. The TF...
4.
5.
Goudelin M, Evrard B, Donisanu R, Gonzalez C, Truffy C, Orabona M, et al.
Ann Intensive Care
. 2024 Jul;
14(1):119.
PMID: 39073505
Background: The objective was to assess the agreement between therapeutic proposals derived from basic critical care echocardiography performed by novice operators in ultrasonography after a limited training (residents) and by...
6.
Lequain H, Streichenberger N, Gallay L, Gerfaud-Valentin M, Fenouil T, Bonjour M, et al.
Neuromuscul Disord
. 2024 Jul;
42:5-13.
PMID: 39059057
Granulomatous myositis is a clinical-pathological entity, which has been rarely reported, mostly described in sarcoidosis. Currently, no clear and simple prognostic factor has been identified to predict granulomatous myositis evolution....
7.
Hadjadj J, Nguyen Y, Mouloudj D, Bourguiba R, Heiblig M, Aloui H, et al.
Ann Rheum Dis
. 2024 May;
83(10):1358-1367.
PMID: 38777378
Objectives: Vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic (VEXAS) syndrome is an adult-onset autoinflammatory disease associated with somatic ubiquitin-like modifier-activating enzyme 1 (UBA1) mutations. We aimed to evaluate the efficacy...
8.
Cosson C, Riou R, Patoli D, Niu T, Rey A, Groslambert M, et al.
J Exp Med
. 2024 Mar;
221(5).
PMID: 38530241
NLRP3-associated autoinflammatory disease is a heterogenous group of monogenic conditions caused by NLRP3 gain-of-function mutations. The poor functional characterization of most NLRP3 variants hinders diagnosis despite efficient anti-IL-1 treatments. Additionally,...
9.
Lequain H, Vasseneix C, Kodjikian L, Boursier G, Jamilloux Y, Seve P
Lancet Rheumatol
. 2024 Jan;
5(9):e564.
PMID: 38251500
No abstract available.
10.
Allam C, Mouton W, Testaert H, Ginevra C, Fessy N, Ibranosyan M, et al.
Front Cell Infect Microbiol
. 2023 Nov;
13:1252515.
PMID: 37965258
Introduction: Severe Legionnaires' disease (LD) can lead to multi-organ failure or death in 10%-30% of patients. Although hyper-inflammation and immunoparalysis are well described in sepsis and are associated with high...