[Complement inhibitors: A global point of view]

Autor: A, Pogossian, C, de Moreuil, C, Lemarié, B, Rouvière, M, Delplanque, B, Molina, L, Prophette, E, Le Moigne

Publikováno v: La Revue de medecine interne. 43(12)

Innate immunity, and more specifically the complement system, has arised renewed interest in the medical field in recent years. Many innovative complement-inhibiting drugs have appeared, acting at various levels of the complement cascade. These drugs

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a4a2b2a7f80d252b0c8039d3fb5b46e6
https://pubmed.ncbi.nlm.nih.gov/36460439

Tattooing and autoinflammatory diseases: a study among 197 French patients from the JIR cohort

Autor: N. Kluger, R. Bourguiba, M. Delplanque, V. Hentgen, I. Kone‐Paut, L. Savey, G. Grateau, S. Georgin‐Lavialle

Publikováno v: Journal of the European Academy of Dermatology and Venereology. 36

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c688a6e14eb34c147b04a92bf19e798
https://doi.org/10.1111/jdv.17886

USAID Associated with Myeloid Neoplasm and VEXAS Syndrome: Two Differential Diagnoses of Suspected Adult Onset Still’s Disease in Elderly Patients

Autor: Achille Aouba, Julien Rossignol, Matthieu Mahévas, Damien Roos-Weil, Pierre Hirsch, Anna Sevoyan, Yervand Hakobyan, Sébastien Miranda, Louis Terriou, Julie Graveleau, Gwenola Maigne, Matthieu Groh, Thomas Quemeneur, Florent Malard, Marie Sebert, Sophie Georgin-Lavialle, Artem Oganesyan, Arsène Mekinian, Nabil Belfeki, Pierre Fenaux, Matthieu Decamp, Laurent Sailler, Louis Drevon, M. Delplanque, Jerome Razanamahery

Publikováno v: Journal of Clinical Medicine
Journal of Clinical Medicine, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine, MDPI, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine; Volume 10; Issue 23; Pages: 5586
Journal of Clinical Medicine, Vol 10, Iss 5586, p 5586 (2021)

International audience; Background: Patients with solid cancers and hematopoietic malignancy can experience systemic symptoms compatible with adult-onset Still’s disease (AOSD). The newly described VEXAS, associated with somatic UBA1 mutations, exh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00e2e510246a9ef755fc33b3b1a67b40
https://hal.sorbonne-universite.fr/hal-03511806/document

Is neutrophilic dermatosis a manifestation of familial Mediterranean fever?

Autor: P Moguelet, Stéphanie Ducharme-Bénard, M. Delplanque, Gilles Grateau, F Chasset, S Georgin-Lavialle, C. Bachmeyer

Publikováno v: Scandinavian journal of rheumatology. 51(1)

Objectives: Familial Mediterranean fever (FMF) is the most frequent monogenic autoinflammatory disease. It is associated with MEFV mutations. Its main features are recurrent episodes of fever and serositis. Patients can display dermatological manifes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d98c5246dc7908c4ffd17f2a5465287
https://pubmed.ncbi.nlm.nih.gov/34159892

Maladie de Still et PseudoStill associés aux SMD et LMMC : Étude nationale Française

Autor: Julie Graveleau, M. Delplanque, Florent Malard, S. guillet, M. Sebert, N. Belfeki, Pierre Hirsch, Sébastien Miranda, Louis Terriou, Damien Roos-Weil, Thomas Quemeneur, S. Georgin-Lavialle, Matthieu Mahevas, G. Maigné, Albertine Aouba, Pierre Fenaux, J. Razanamahery, Laurent Sailler, A. Mekinian, M. Groh

Publikováno v: La Revue de Médecine Interne. 42:A54-A55

Introduction Dix a 20 % des syndromes myelodysplasiques (SMD)/Leucemies myelomonocytaires chroniques (LMMC) pourraient etre associes a diverses pathologies extra-hematologiques telles que des dermatoses neutrophiles, des vascularites systemiques, des

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d6807548918c5d028b21bfa75f7b994
https://doi.org/10.1016/j.revmed.2021.03.259