Search Results - "Ebbo, M."

Haematological immune-related adverse events with immune checkpoint inhibitors, how to manage? by Michot, J.M., Lazarovici, J., Tieu, A., Champiat, S., Voisin, A.L., Ebbo, M., Godeau, B., Michel, M., Ribrag, V., Lambotte, O.

“…Immune checkpoint inhibitors (ICIs) are changing the treatments of many patients with cancer. These immunotherapies are generally better tolerated than…”
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IgG4-related disease: Diagnostic criteria evolution toward the 2019 ACR/EULAR classification criteria by Schleinitz, N, Briantais, A, Ebbo, M

“…The concept of IgG4-related disease (IgG4-RD) has recently been individualized in the early 2000s, but most of the organ involvements are known since more than…”
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Adult immune thrombocytopenia and thrombopoietin receptor agonist: Ten years later by Ebbo, M, Rivière, E, Godeau, B

“…Ten years after their licence in France, the use of the two thrombopoietin receptor agonists (TPO-RA), eltrombopag and romiplostim, has deeply modified the…”
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Large-vessel involvement in ANCA-associated vasculitis: A multicenter case-control study by Monghal, V., Puéchal, X., Smets, P., Vandergheynst, F., Michel, M., Diot, E., Ramdani, Y., Moulinet, T., Dhote, R., Hautcoeur, A., Lelubre, C., Dominique, S., Lebourg, L., Melboucy, S., Wauters, N., Carlotti, A., Cachin, F., Ebbo, M., Jourde-Chiche, N., Iudici, M., Aumaitre, O., Andre, M., Terrier, B., Trefond, L.

“…Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) primarily affects small vessels. Large-vessel involvement (LVI) is rare. We aimed to…”
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Cyclophosphamide vs rituximab for eradicating inhibitors in acquired hemophilia A: A randomized trial in 108 patients by Lévesque, H., Viallard, J.F., Houivet, E., Bonnotte, B., Voisin, S., Le Cam-Duchez, V., Maillot, F., Lambert, M., Liozon, E., Hervier, B., Fain, O., Guillet, B., Schmidt, J., Luca, L.E., Ebbo, M., Ferreira-Maldent, N., Babuty, A., Sailler, L., Duffau, P., Barbay, V., Audia, S., Benichou, J., Graveleau, J., Benhamou, Y.

“…Acquired hemophilia A (AHA) is a rare autoimmune disorder due to autoantibodies against Factor VIII, with a high mortality risk. Treatments aim to control…”
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Intravenous immunoglobulin as a rescue therapy for severe adult autoimmune hemolytic anemia: Results from a French multicenter observational study by Michel, M., Saïr, M., Rivière, E., Moulis, G., Comont, T., Costedoat‐Chalumeau, N., Pouchelon, C., Boutboul, D., Benyamine, A., Bert, A., Jeandel, P. ‐Y., Hamrouni, S., Belfeki, N., Lobbes, H., Dossier, A., Gobert, D., Mahevas, M., Godeau, B., Gallien, Y., Ebbo, M.

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IgG4 hypophysitis: Diagnosis and management by Lojou, M., Bonneville, J.F., Ebbo, M., Schleinitz, N., Castinetti, F.

“…IgG4-related hypophysitis is a rare disease, due to a lymphoplasmocytic IgG4 positive infiltration of the pituitary. Literature data are scarce, even though…”
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NK cell compartment in the peripheral blood and spleen in adult patients with primary immune thrombocytopenia by Ebbo, M, Audonnet, S, Grados, A, Benarous, L, Mahevas, M, Godeau, B, Viallard, J.F, Piperoglou, C, Cognet, C, Farnarier, C, Harlé, J.R, Schleinitz, N, Vély, F

“…Abstract Immune thrombocytopenic purpura (ITP) is a disease characterized by antibody-mediated platelet destruction. The T- and B-cell subsets have been…”
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IVIg increases interleukin‐11 levels, which in turn contribute to increased platelets, VWF and FVIII in mice and humans by Nguyen, A., Repesse, Y., Ebbo, M., Allenbach, Y., Benveniste, O., Vallat, J. M., Magy, L., Deshayes, S., Maigné, G., Boysson, H., Karnam, A., Delignat, S., Lacroix‐Desmazes, S., Bayry, J., Aouba, A.

“…Summary The mechanisms of action of intravenous immunoglobulins (IVIg) in autoimmune diseases are not fully understood. The fixed duration of efficacy and…”
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Hospitalization for infection in patients treated for giant cell arteritis: A single-centre retrospective study by Lavrard-Meyer, P, Gomes De Pinho, Q, Daumas, A, Benyamine, A, Ebbo, M, Schleinitz, N, Harlé, J R, Jarrot, P A, Kaplanski, G, Berbis, J, Granel, B

“…Infections are associated with morbimortality of patients with giant cell arteritis (GCA). The aim of this work was twofold: the identification of factors…”
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A descriptive study of IgG4-related disease in children and young adults by de Sainte Marie, B., Ebbo, M., Grados, A., Rebours, V., Reumaux, H., Briantais, A., Urbina, D., Cury, J., Morel, N., Lhote, F., Rohmer, B., Lazaro, E., Agbo-Kpati, K.P., Deroux, A., Domont, F., Delacroix, I., Lavigne, C., Perlat, A., Kahn, J.E., Godeau, B., Hamidou, M., Launay, D., Bader-Meunier, B., Schleinitz, N.

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Gaucher Disease type 1 mimicking immune thrombocytopenia: Role of hyperferritinemia and hypergammaglobulinemia in the initial evaluation of an isolated thrombopenia by Faucher, B, Seguier, J, Swiader, L, Cuquemelle, C, Cerutti, D, Ebbo, M

“…Gaucher disease type 1 is a rare genetic disease. It can cause thrombocytopenia. Current guidelines do not support bone marrow examination in front of isolated…”
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Bilateral adrenal hemorrhage under apixaban in primary antiphospholipid syndrome by Lavoipierre, V, Talbot, M, Soubrier, C, De Sainte Marie, B, Seux, V, Solas, C, Morange, P, Bernit, E, Ebbo, M, Faucher, B, Harlé, J R, Schleinitz, N

“…Adrenal hemorrhage is a classical but rare complication of antiphospholipid syndrome, revealing diagnosis in one third of the cases. Anti-vitamin K therapy is…”
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Expectation of patients and caregivers about patient education for immune thrombocytopenia by Mettler, C, Daguzan, A, Lagouanelle, M-C, Briantais, A, Ducros, P, Laborde, S, Gouiran, S, Schleinitz, N, Faucher, B, Ebbo, M

“…Immune thrombocytopenia (ITP) durably affects quality of life in patients. Patient education aims at improving their self-care and psychosocial skills,…”
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Ocular syphilis, a re-emergent pathology: Series of 12 patients in one Hospital, 2017 by Gutierrez, B, Gayet, S, Bertolino, J, Jean, E, Le Goff, L, Voisin, H, Sampo, M, Meunier, B, Harle, J-R, Ebbo, M, Schleinitz, N, Menard, A, Bernit, E

“…Syphilis is a sexually transmitted disease. All organs might be affected, but ocular syphilis only occurs in 0.6 percent of patients. We collected all cases of…”
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Characteristics of giant cell arteritis patients under and over 75-years-old: A comparative study on 164 patients by Daumas, A, Bichon, A, Rioland, C, Benyamine, A, Berbis, J, Ebbo, M, Jarrot, P-A, Gayet, S, Rossi, P, Schleinitz, N, Harle, J-R, Kaplanski, G, Villani, P, Granel, B

“…Giant cell arteritis (GCA) is the most common vasculitis of the elderly. In order to assess the impact of age at diagnosis, we compared the characteristics of…”
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IgG4-related disease treatment in 2014: Update and literature review by Grados, A, Ebbo, M, Jean, E, Bernit, E, Harlé, J-R, Schleinitz, N

“…IgG4-related disease is an inflammatory disorder characterized by a polyclonal lymphoplasmacytic tissue infiltrate, with numerous IgG4+ plasmocytes, evolving…”
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Eye and skin lesions by Gomes de Pinho, Q, de Sainte Marie, B, Seguier, J, Ebbo, M, Schleinitz, N

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Long-lasting thrombocytopenia induced by glycoprotein IIb/IIIa inhibitor by Christen, J-R, Soubrier, C, Martinez, E, Roumieu, V, Darmon, O, Scandaliaris, S, Picou, L, Cuisset, T, Grados, A, Bernit, E, Ebbo, M, Harlé, J-R, Schleinitz, N

“…Glycoprotein IIb/IIIa inhibitors (anti-GPIIbIIIa) prevent platelet binding to fibrinogen. Transient sometimes-severe thrombocytopenia is a well-known side…”
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IgG4-related systemic disease: emergence of a new systemic disease? Literature review by Ebbo, M, Grados, A, Daniel, L, Vély, F, Harlé, J-R, Pavic, M, Schleinitz, N

“…Hyper-IgG4 syndrome, or IgG4-related systemic disease (IgG4-RSD), has been recently characterized by the association of a focal or diffuse enlargement in one…”
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