Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sylvie Sauvion"'
Autor:
L. de Pontual, M. Simonin, Aurelien Galerne, V. Meignin, Sylvie Sauvion, A. Escudier, M. Houlier, S. Abbou, Joël Gaudelus, S. Courbage
Publikováno v:
Archives de Pédiatrie. 24:471-475
Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis, is a rare cause of lymphadenopathy in children. This benign disease can mimic lymphoma and misleads doctors. It was first described in Asia, where it occurred especially i
Autor:
Pierre Quartier, Julie Bruneau, Sylvain Breton, Marie-Claude Stolzenberg, Patrick Nitschke, Aude Magerus-Chatinet, Benedicte Neven, Sylvie Sauvion, Frédéric Rieux-Laucat, Alain Fischer, Mohammed Zarhrate, Eva Lévy
Publikováno v:
Clinical Immunology. 168:88-93
LRBA (lipopolysaccharide-responsive and beige-like anchor protein) deficiency associates immune deficiency, lymphoproliferation, and various organ-specific autoimmunity. To date, prevalent symptoms are autoimmune cytopenias and enteropathy, and lymph
Autor:
Sylvie Sauvion, Loïc de Pontual, Tewfik Bibi-Triki, Joël Gaudelus, Valérie Bélien, Emeline Chapelon, Yves Laurian
Publikováno v:
Annales de biologie clinique. 69:481-484
An 11 year old African boy without previous history was hospitalised for fever and a severe anaemia (haemoglobin = 55 g/L) with low reticulocyte count. Blood smear showed more than 35% of ghost red blood cells which allows the diagnosis of G6PD defic
Autor:
Nehla Ghedira, Nathalie Pouvreau, Yline Capri, Odile Fenneteau, Joelle Roume, Aurélie Caye, Bérénice Doray, Laurence Perrin, Odile Boute, Natacha Fillot, Aurélien Trimouille, Cédric Vignal, Yves Alembik, Patricia Blanchet, Valérie Drouin-Garraud, Bertrand Isidor, Marlène Rio, Marion Gérard, Jean-Luc Alessandri, Annick Toutain, Alain Verloes, Albert David, Hélène Cavé, Anne Dieux Coeslier, Clarisse Baumann, Olivier Dulac, Delphine Héron, Sylvie Sauvion, Catherine Vincent-Delorme, Stanislas Lyonnet, Marjorie Willems, Patrice Bouvagnet, Didier Lacombe
Publikováno v:
European journal of human genetics : EJHG. 24(8)
Noonan syndrome is a heterogeneous autosomal dominant disorder caused by mutations in at least eight genes involved in the RAS/MAPK signaling pathway. Recently, RIT1 (Ras-like without CAAX 1) has been shown to be involved in the pathogenesis of some
Autor:
Séverine Cunat, Yves Deugnier, Anne-Marie Jouanolle, Patricia Aguilar-Martinez, Edouard Bardou-Jacquet, Bruno Pouliquen, Xavier Causse, Pierre Brissot, Véronique David, Caroline Kannengiesser, Olivier Loréal, Sylvie Sauvion, Marie-Pascale Beaumont-Epinette
Publikováno v:
British Journal of Haematology
British Journal of Haematology, Wiley, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
British Journal of Haematology, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
British Journal of Haematology, Wiley, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
British Journal of Haematology, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8b25fc53c04328ddc964b046188f3ba
https://www.hal.inserm.fr/inserm-00836894
https://www.hal.inserm.fr/inserm-00836894
Autor:
Joël Gaudelus, Stéphane Blanche, Marianne Besnard, Sylvie Sauvion, Catherine Offredo, Florence Veber, Jean-Louis Gaillard
Publikováno v:
The Pediatric infectious disease journal. 12(12)
The use of Mycobacterium bovis/Bacillus Calmette-Guerin (BCG) to vaccinate against tuberculosis remains controversial. The development of tuberculosis in human immunodeficiency virus (HIV)-infected children demands specific evaluation of the risk/ben