Zobrazeno 1 - 10
of 206
pro vyhledávání: '"J -L. Pasquali"'
Autor:
Laurent Arnaud, Zahir Amoura, Thierry Martin, Anne-Sophie Korganow, Aurélien Guffroy, Jean Sibilia, François Maurier, Bernard Bonnotte, Andreas Schwarting, Gilles Blaison, Pierre Kieffer, Nadine Magy-Bertrand, J Sibilia, Yannick Dieudonne, C Fiehn, M Rizzi, R Voll, Z Amoura, C Sordet, M Bartsch, A Schwarting, L Arnaud, Christoph Fiehn, JE Gottenberg, R Max, H-H Peter, J-L Pasquali, T Martín, A Meyer, J Thiel, P Kieffer, N Venhoff, H Lorenz, F Maurier, Aurore Meyer, Hannes Martin Lorenz, Jean-Louis Pennaforte, Hans-Hartmut Peter, Reinhard Edmund Voll, G Blaison, B Bonnotte, E Chatelus, E Ciobanu, F Duchene, JP Faller, A Gorse, O Hinschberger, F Jaeger, M Kilifa, N Magy-Bertrand, L Martzolff, J-L Pennaforte, V Poindron, S Revuz, M Samson, A Theulin, D Wahl, JC Weber, N Bartholomä, S Finzel, A Funkert, M Hausberg
Publikováno v:
Lupus Science and Medicine, Vol 7, Iss 1 (2020)
Objective Systemic lupus is a chronic autoimmune disease characterised by its phenotypic heterogeneity. Neutropaenia is a frequent event in SLE occurring in 20%–40% of patients depending on the threshold value of neutrophil count. On a daily basis,
Externí odkaz:
https://doaj.org/article/af7b091098c243df9c71de7528e7d046
Autor:
M. Even, J.-L. Pasquali, R. Fior, T. Thubert, Olivier Picone, Alexandra Benachi, René Frydman, C. Dupont-Bernabe, A.-C. Donnadieu
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 40:283-290
Resume La maladie de Behcet est une maladie systemique d’etiologie inconnue caracterisee par une aphtose bipolaire (buccale et genitale) recidivante associee a des manifestations oculaires, cutanees, vasculaires, digestives ou articulaires. Les gyn
Autor:
Claverie, Nicole1, J -L. Pasquali2, Mamont, P. S.1, Danzin, C.1, Weil-Bousson, Marguerite3, Siat, Marlyse1
Publikováno v:
Clinical & Experimental Immunology. May1988, Vol. 72 Issue 2, p293-298. 6p.
Publikováno v:
Revue de Pneumologie Clinique. 60:175-179
Resume Certains desordres de la coagulation peuvent etre observes chez les patients atteints de cancer, et les complications thromboemboliques apparaissent comme une complication frequente. Nous rapportons le cas d’un patient de 53 ans presentant u
Autor:
Nadine Magy-Bertrand, Pierre Kaminsky, A-C Rat, Stéphane Zuily, B. Lorcerie, Francis Guillemin, N. Baillet, Véronique Regnault, Jacques Ninet, P. Mismetti, Denis Wahl, J-L Pasquali, E Pasquier, Marc Lambert, T. Lecompte
Publikováno v:
Lupus
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-8. ⟨10.1177/0961203315580871⟩
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-8. 〈10.1177/0961203315580871〉
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-1168. ⟨10.1177/0961203315580871⟩
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-8. ⟨10.1177/0961203315580871⟩
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-8. 〈10.1177/0961203315580871〉
Lupus, SAGE Publications, 2015, 24 (11), pp.1161-1168. ⟨10.1177/0961203315580871⟩
Objectives Health-related quality of life (HRQoL) has not been fully explored in antiphospholipid syndrome (APS); therefore, we compared HRQoL between APS patients and the general population and assessed the impact of thromboembolic history. Methods
Autor:
L. U. Philippe, B. Gustafson, L. Dahlberg, J. Sibilia, E. Lee, J. L. Pasquali, Hiroshi Fujii, Y. Song, J. Sibila, J. Goronzy, K. Fujio, Y. Hong, J. Kang, T. Eisler, I. Colmegna, P. Soulas-Sprauel, J. Gottenberg, H. Harigae, M Gattorno, Tomonori Ishii, A. François, Silvia Federici, Federica Penco, L. Shao, D. Wachsmann, Denise Lasigliè, U. Smith, M. Bokarewa, J. E. Gottenberg, A. Ekwall, H. Shoda, E. A. Boström, W. Cornellia, W. Lee, M. Svensson, S. Bae, A. Martini, G. Alsaleh, JL Park, S. Andersson, Kazuhiko Yamamoto, Elisabetta Traggiai, J. Kim
Publikováno v:
International Immunology. 22:ii93-ii95
Autor:
Eric Epailly, Hélène Petit, Bernard Eisenmann, J. L. Pasquali, François Levy, Nabil Chakfe, Philippe Nicolini, J. G. Kretz
Publikováno v:
European Journal of Vascular and Endovascular Surgery. 12(3):346-353
Aim: To compare the peroperative blood loss and the postoperative systemic inflammatory reaction in patients receiving either a Vasculour II Albumin pre-impregnated prosthesis (VA group, n = 32) or a preclotted Vasculour II prosthesis (V group, n = 3
Publikováno v:
Clinical and Experimental Immunology. 103:171-175
SUMMARY Antiphospholipid antibodies (APL) are usually detected using solid-phase immunoassays, where cardiolipin is the most common capture antigen. Phosholipids are believed to adopt a monolayer organization when coated onto polystyrene after evapor
Publikováno v:
The Journal of Immunology. 154:4526-4535
Monoreactive high affinity pathologic autoantibodies were supposed previously to derive through somatic mutation from polyreactive low affinity autoantibodies that are encoded by a small set of unmutated V region genes in fetal and neonatal B cells.
Publikováno v:
The Journal of Immunology. 154:413-421
Mixed cryoglobulinemia is usually considered to be a nonmalignant human B cell proliferation that produces a monoclonal IgM rheumatoid factor (RF). Important immunologic similarities and differences were described between the monoclonal B cells durin