Eosinophilic granulomatosis with polyangiitis (Churg‐Strauss): clinical characteristics and long‐term followup of the 383 patients enrolled in the French Vasculitis …

…, O Aumaître, GL Guenno, AL Quellec… - Arthritis & …, 2013 - Wiley Online Library
Objective Earlier studies of eosinophilic granulomatosis with polyangiitis (Churg‐Strauss) (EGPA),
with limited patient numbers and followup durations, demonstrated that clinical …

Adult onset Still's disease (AOSD) in the era of biologic therapies: dichotomous view for cytokine and clinical expressions

ATJ Maria, A Le Quellec, C Jorgensen, I Touitou… - Autoimmunity …, 2014 - Elsevier
Adult onset Still's disease (AOSD) is a rare inflammatory disorder characterized by hectic
spiking fever, evanescent rash and joint involvement. Prognosis is highly variable upon …

MEFV mutations in Behçet's disease

…, X Magne, N Molinari, A Navarro, AL Quellec… - Human …, 2000 - Wiley Online Library
Familial Mediterranean fever (FMF) and Behçet's disease (BD), both inflammatory diseases,
are highly prevalent in the Middle Eastern and Mediterranean populations. FMF is a …

Adipose-derived mesenchymal stem cells in autoimmune disorders: state of the art and perspectives for systemic sclerosis

ATJ Maria, M Maumus, A Le Quellec… - Clinical reviews in …, 2017 - Springer
Mesenchymal stromal/stem cells (MSC) are non-hematopoietic multipotent progenitor cells,
first described in bone marrow in the middle of last century. Since then, MSC have been the …

[HTML][HTML] Mastitis in autoimmune diseases: review of the literature, diagnostic pathway, and pathophysiological key players

…, I Millet, ATJ Maria, J Morel, A Le Quellec… - Journal of Clinical …, 2020 - mdpi.com
Mastitis frequently affects women of childbearing age. Of all the pathological breast conditions
requiring specific management, autoimmune mastitis is in the third position after infection …

Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

…, F Lanternier, C Larroche, A Le Quellec… - Journal of Allergy and …, 2017 - Elsevier
Background Primary immunodeficiencies (PIDs) are inherited diseases associated with a
considerable increase in susceptibility to infections. It is known that PIDs can also predispose …

The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty‐seven patients

…, B Flageul, A Deroux, A Le Quellec… - Arthritis & …, 2015 - Wiley Online Library
Objective Hypocomplementemic urticarial vasculitis (HUV) is an uncommon vasculitis of
unknown etiology that is rarely described in the literature. We undertook this study to analyze …

Adverse drug events associated with hospital admission

…, D Hillaire-Buys, A Le Quellec… - Annals of …, 2003 - journals.sagepub.com
OBJECTIVE To increase the knowledge base on the frequency, causality, and avoidability
of adverse drug events (ADEs) as a cause for admission in internal medicine or when …

Human adipose mesenchymal stem cells as potent anti-fibrosis therapy for systemic sclerosis

…, K Toupet, M Maumus, G Fonteneau, A Le Quellec… - Journal of …, 2016 - Elsevier
Objectives Displaying immunosuppressive and trophic properties, mesenchymal stem/stromal
cells (MSC) are being evaluated as promising therapeutic options in a variety of …

Central nervous system involvement of granulomatosis with polyangiitis: clinical–radiological presentation distinguishes different outcomes

G De Luna, B Terrier, P Kaminsky, A Le Quellec… - …, 2015 - academic.oup.com
Objective. The aim of this study was to describe the presentation and outcomes of patients
with granulomatosis with polyangiitis (GPA) presenting with CNS involvement. Methods. …