Search Results - "Jeandel, P. ‐Y."

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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Tranexamic acid as maintenance treatment for non‐histaminergic angioedema: analysis of efficacy and safety in 37 patients by Wintenberger, C., Boccon‐Gibod, I., Launay, D., Fain, O., Kanny, G., Jeandel, P. Y., Martin, L., Gompel, A., Bouillet, L.

“…Summary Angioedema (AE) is a clinical syndrome characterized by localised swelling lasting several hours. The swelling is often recurring and can be lethal if…”
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The tyrosine kinase Syk regulates the survival of chronic lymphocytic leukemia B cells through PKCδ and proteasome-dependent regulation of Mcl-1 expression by Baudot, A D, Jeandel, P Y, Mouska, X, Maurer, U, Tartare-Deckert, S, Raynaud, S D, Cassuto, J P, Ticchioni, M, Deckert, M

“…B-cell chronic lymphocytic leukemia (B-CLL) is characterized by accumulation of mature monoclonal CD5+ B cells. The disease results mainly from a failure of…”
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Homeostatic chemokines increase survival of B-chronic lymphocytic leukemia cells through inactivation of transcription factor FOXO3a by TICCHIONI, M, ESSAFI, M, JEANDEL, P. Y, DAVI, F, CASSUTO, J. P, DECKERT, M, BERNARD, A

“…B-chronic lymphocytic leukemia (B-CLL) cell is characterized by the accumulation of long-lived CD5+ B lymphocytes, whose survival in vivo is in part dependent…”
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Contrast-Enhanced Ultrasound of Carotid Artery Wall in Takayasu Disease: First Evidence of Application in Diagnosis and Monitoring of Response to Treatment by GIORDANA, P, BAQUE-JUSTON, M. C, JEANDEL, P. Y, MONDOT, L, HIRLEMANN, J, PADOVANI, B, RAFFAELLI, C

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Successful treatment with rituximab of one patient with CANOMAD neuropathy by Delmont, Emilien, Jeandel, P. Y., Hubert, A. M., Marcq, L., Boucraut, J., Desnuelle, C.

“…We report a successful treatment with rituximab in a patient with CANOMAD neuropathy resistant to previous therapy. The titers of anti-disialosyl antibodies…”
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The tyrosine kinase Syk regulates the survival of chronic lymphocytic leukemia B cells through PKC[delta] and proteasome-dependent regulation of Mcl-1 expression by Baudot, A D, Jeandel, P Y, Mouska, X, Maurer, U, Tartare-deckert, S, Raynaud, S D, Cassuto, J P, Ticchioni, M, Deckert, M

“…B-cell chronic lymphocytic leukemia (B-CLL) is characterized by accumulation of mature monoclonal CD5+ B cells. The disease results mainly from a failure of…”
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Acquired angioedema due to C1-inhibitor deficiency: CREAK recommendations for diagnosis and treatment by Gobert, D, Bouillet, L, Armengol, G, Coppo, P, Defendi, F, Du-Thanh, A, Hardy, G, Javaud, N, Jeandel, P-Y, Launay, D, Panayotopoulos, V, Pelletier, F, Boccon-Gibod, I, Fain, O

“…Acquired angioedema with C1-inhibitor deficiency is a rare and peculiar entity belonging to the spectrum of bradykinin angioedemas. It usually occurs in…”
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FDG-PET/CT findings in systemic mastocytosis: a French multicentre study by Djelbani-Ahmed, S., Chandesris, M. O., Mekinian, A., Canioni, D., Brouzes, C., Hanssens, K., Pop, G., Durieu, I., Durupt, S., Grosbois, B., Besnard, S., Tournilhac, O., Beyne-Rauzy, O., Agapé, P., Delmer, A., Ranta, D., Jeandel, P. Y., Georgin-Lavialle, S., Frenzel, L., Damaj, G., Eder, V., Lortholary, O., Hermine, O., Fain, O., Soussan, M.

“…Introduction Mastocytosis is a clonal haematological disease characterized by uncontrolled proliferation and the activation of mast cells. The value of…”
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Hereditary angioedema and lupus: A French retrospective study and literature review by Gallais Sérézal, Irène, Bouillet, Laurence, Dhôte, Robin, Gayet, Stéphane, Jeandel, Pierre-Yves, Blanchard-Delaunay, Claire, Martin, Ludovic, Mekinian, Arsène, Fain, Olivier

“…Abstract Hereditary angioedema (HAE) is a rare genetic disorder that is primarily caused by a defect in the C1 inhibitor (C1-INH). The recurrent symptoms are…”
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Treatment with rituximab in patients with polyneuropathy with anti-MAG antibodies by Delmont, Emilien, Jeandel, P. Y., Benaïm, C., Rosenthal, E., Fuzibet, J. G., Desnuelle, C.

“…We report on a series of six patients diagnosed as anti-MAG polyneuropathy treated with rituximab. Nine months after the infusion of rituximab, sensory…”
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Improvement of severe and intravenous immunoglobulin-dependent multifocal motor neuropathy with conduction block after long-term rituximab by Michaud, A, Delmont, E, Jeandel, P-Y, Desnuelle, C

“…Some patients suffering from multifocal motor neuropathy with conduction blocks (MMNCB) are still disabled after treatment with intravenous immunoglobulin…”
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Efficacy of autologous peripheral blood stem cell transplantation (auto-PBSCT) on the neuropathic manifestations in POEMS syndrome by Gronier, S, Delmont, E, Legros, L, Launay, M, Jeandel, P Y, Fuzibet, J G, Desnuelle, C

“…POEMS syndrome (polyneuropathy, organomegaly, endocrynopathy, M-protein, and skin changes) is a rare multisystem disease associated with plasma cell dyscrasia…”
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Un diagnostic tiré par les cheveux by Tieulié, N., Jeandel, P.-Y., Heudier, P., Roth, S., Sanderson, F., Rosenthal, E., Fuzibet, J.-G., Rivière, S.

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Amélioration d’un cas de neuropathie motrice multifocale avec blocs de conduction sévère, dépendant des immunoglobulines intraveineuses, après adjonction de rituximab au long cours by Michaud, A., Delmont, E., Jeandel, P.-Y., Desnuelle, C.

“…Certains patients atteints de neuropathie motrice multifocale avec blocs de conduction (NMMBC) restent handicapés malgré un traitement par immunoglobulines…”
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Hereditary Angioedema with and Without C1-Inhibitor Deficiency in Postmenopausal Women by Billebeau, Aurore, Fain, Olivier, Launay, David, Boccon-Gibod, Isabelle, Bouillet, Laurence, Gobert, Delphine, Plu-Bureau, Geneviève, Gompel, Anne

“…Purpose Most types of hereditary angioedema (HAE) are worsened by endogenous or exogenous estrogens. Conversely, androgens can improve HAE with abnormal…”
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Liposomal amphotericin B as treatment for visceral leishmaniasis in Europe, 2009 by Rosenthal, E, Delaunay, P, Jeandel, P-Y, Haas, H, Pomares-Estran, C, Marty, P

“…Visceral leishmaniasis (VL) causes an estimated 500,000 new cases of disease and more than 50,000 deaths a year. For more than 60 years, pentavalent antimonies…”
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BCL-B (BCL2L10) is overexpressed in patients suffering from multiple myeloma (MM) and drives an MM-like disease in transgenic mice by Hamouda, Mohamed-Amine, Jacquel, Arnaud, Robert, Guillaume, Puissant, Alexandre, Richez, Valentine, Cassel, Romeo, Fenouille, Nina, Roulland, Sandrine, Gilleron, Jerome, Griessinger, Emmanuel, Dubois, Alix, Bailly-Maitre, Beatrice, Goncalves, Diogo, Mallavialle, Aude, Colosetti, Pascal, Marchetti, Sandrine, Amiot, Martine, Gomez-Bougie, Patricia, Rochet, Nathalie, Deckert, Marcel, Avet-Loiseau, Herve, Hofman, Paul, Karsenti, Jean-Michel, Jeandel, Pierre-Yves, Blin-Wakkach, Claudine, Nadel, Bertrand, Cluzeau, Thomas, Anderson, Kenneth C, Fuzibet, Jean-Gabriel, Auberger, Patrick, Luciano, Frederic

“…Multiple myeloma (MM) evolves from a premalignant condition known as monoclonal gammopathy of undetermined significance (MGUS). However, the factors underlying…”
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The Icatibant Outcome Survey: experience of hereditary angioedema management from six European countries by Caballero, T., Aberer, W., Longhurst, H.J., Maurer, M., Zanichelli, A., Perrin, A., Bouillet, L., Andresen, I., Arcoleo, F., Bova, M., Cicardi, M., Cillari, E., Montinaro, V., Marone, G., Blanchard Delauny, C., Boccon‐Gibod, I., Coppere, B., Dzviga, C., Fain, O., Goichot, B., Gompel, A., Guez, S., Jeandel, P.Y., Kanny, G., Launay, D., Maillard, H., Martin, L., Masseau, A., Ollivier, Y., Magerl, M., Baeza, M.L., Cabañas, R., Guilarte, M., Hernández, D., Hernando de Larramendi, C., Lleonart, R., Lobera, T., Marqués, L., Bangs, C., Buckland, M., Grigoriadou, S., Helbert, M., Lorenzo, L.

“…Background Hereditary angioedema (HAE) due to C1‐inhibitor deficiency (C1‐INH‐HAE) is a rare, potentially fatal, bradykinin‐mediated disease. Icatibant is a…”
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Un cas de réticulohistiocytose multicentrique paranéoplasique associée à une maladie cœliaque by Roth, S., Campagni, J.P., Perrin, C., Sanderson, F., Castela, J., Rosenthal, E., Tieulié, N., Jeandel, P.Y., Heudier, P., Fuzibet, J.G.

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