Immune recovery uveitis in Whipple’s disease: an unusual ocular presentation

Autor: Hippolyte Lequain, Stéphane Abramowicz, Julien Seiller, Amro Abukhashbah, Carole Burillon, Emmanuelle Vignot, Olivier Brunet, Pascal Sève

Publikováno v: Journal of Ophthalmic Inflammation and Infection, Vol 14, Iss 1, Pp 1-7 (2024)

Abstract Purpose To describe an unusual case of Whipple’s disease (WD) complicated by uveitis, and subsequent paradoxical worsening after effective antibiotic treatment targeting Tropheryma whipplei (TW). Methods Case report. Results A 53-year-old

Externí odkaz: https://doaj.org/article/e2268d3bc2fe40908133a4847bf9fc64

X-Linked Hypophosphatemia, Not Only a Skeletal Disease But Also a Chronic Inflammatory State

Autor: Marie-Noëlle Méaux, Candide Alioli, Agnès Linglart, Sandrine Lemoine, Emmanuelle Vignot, Aurélia Bertholet-Thomas, Olivier Peyruchaud, Sacha Flammier, Irma Machuca-Gayet, Justine Bacchetta

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 107:3275-3286

Context X-linked hypophosphatemia (XLH) is a rare genetic disease caused by a primary excess of fibroblast growth factor 23 (FGF23). FGF23 has been associated with inflammation and impaired osteoclastogenesis, but these pathways have not been investi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab22ff6f6ae6387808e32225872ae4d7
https://doi.org/10.1210/clinem/dgac543

The Spectrum of Still's Disease: A Comparative Analysis of Phenotypic Forms in a Cohort of 238 Patients

Autor: Pierre-Antoine Neau, Thomas El-Jammal, Clément Javaux, Nicolas Fournier, Orlane Chol, Léopold Adelaïde, Kim Heang Ly, Mathieu Gerfaud-Valentin, Laurent Perard, Marine Fouillet-Desjonqueres, Julie Le Scanff, Emmanuelle Vignot, Arnaud Hot, Alexandre Belot, Isabelle Durieu, Pascal Sève, Yvan Jamilloux

Publikováno v: Journal of Clinical Medicine; Volume 11; Issue 22; Pages: 6703

Still’s disease (SD) is a heterogeneous autoinflammatory disorder for which several phenotypes have been described. We conducted a retrospective study to re-evaluate the dichotomous view of the disease, to compare the juvenile and adult forms, and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ad59d968db3b9211061bd329c4f924
https://pubmed.ncbi.nlm.nih.gov/36431180

Detection and Prediction of Macrophage Activation Syndrome in Still’s Disease

Autor: Clément Javaux, Thomas El-Jammal, Pierre-Antoine Neau, Nicolas Fournier, Mathieu Gerfaud-Valentin, Laurent Perard, Marine Fouillet-Desjonqueres, Julie Le Scanff, Emmanuelle Vignot, Stéphane Durupt, Arnaud Hot, Alexandre Belot, Isabelle Durieu, Thomas Henry, Pascal Sève, Yvan Jamilloux

Publikováno v: Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 11, Iss 206, p 206 (2022)
Journal of Clinical Medicine; Volume 11; Issue 1; Pages: 206

Distinguishing between macrophage activation syndrome (MAS) and a simple flare of Still’s disease (SD) may be challenging. We sought to clarify the clinical features and outcome of MAS in SD and to explore predictive factors of MAS development. Dem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85935694f4cf9deb6eeb55069c6d8d49
http://europepmc.org/articles/PMC8745834

Dysregulation of MicroRNAs in Osteogenesis Imperfecta: the miROI study

Autor: Alexandre Mercier, Marjorie Millet, Blandine Merle, Olivier Borel, Elisabeth Sornay-Rendu, Pawel Szulc, Emmanuelle Vignot, Deborah Gensburger, Elisabeth Fontanges, Martine Croset, Roland Chapurlat

Publikováno v: Bone Reports. 16:101198

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8fb6a08f4814564532c350d38b53185f
https://doi.org/10.1016/j.bonr.2022.101198