Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Claire Desplantes"'
Autor:
Paul Saultier, Mathieu Simonin, Tiphaine Adam de Beaumais, Fanny Rialland, Fanny Alby-Laurent, Marion Lubnau, Claire Desplantes, Evelyne Jacqz-Aigrain, Pierre Rohrlich, Yves Reguerre, Florence Rabian, Nicolas Sirvent, Geneviève Willson Plat, Arnaud Petit
Publikováno v:
Bulletin du Cancer. 109:1132-1143
Autor:
Laura Olivier-Gougenheim, Wadih Abou-Chahla, Pascale Schneider, Damien Dupont, Sandrine Thouvenin-Doulet, Claire Desplantes, Stéphane Ducassou, Nathalie Cheikh, Claire Freycon, Benoit Brethon, Fanny Rialland, Claire Pluchart, Yves Bertrand, Alexandre Theron, Geneviève Plat, Audrey Contet, Carine Domenech, Virginie Gandemer, Catherine Paillard, Nicolas Rama, Maryline Poirée, Paul Saultier, Elodie Gouache, Guy Leverger, Jérémie Rouger-Gaudichon, Pascale Blouin, Isabelle Pellier, Caroline Oudot
Publikováno v:
The Journal of Pediatrics. 236:204-210
To obtain a national overview of the epidemiology and management of invasive fungal infections (IFIs) in France for severely immunocompromised children who were treated for acute leukemia or had undergone allogeneic hematopoietic stem cell transplant
Autor:
Arnaud Salmon-Rousseau, Pascal Chavanet, Christelle Auvray, Claire Briandet, Quentin Besset, Claire Desplantes
Publikováno v:
Journal of Bone and Joint Infection. 6:171-178
Bartonella henselae is the bacterial agent responsible for cat scratch disease. This infection is frequently the cause of localized lymphadenitis in children. It is also sometimes responsible for endocarditis, encephalitis, hepatic peliosis and in ra
Autor:
Claire Desplantes, Gaelle Roques, Jean Luc Harousseau, Christine bellanne Chantelot, Patrick Lutz, Pierre Morville, Hélène Lapillonne, Lucile Pinson, Agnes Buzyn, Isabelle Pellier, Eric Jeziorski, Capucine Picard, Catherine Paillard, Julie Bruneau, Marie-Louise Frémond, Blandine Beaupain, Norma B. Romero, Jean Pierre Vannier, Florence Bellanger, Loïc de Pontual, Jean Donadieu
Publikováno v:
Europe PubMed Central
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9 (1), pp.183. ⟨10.1186/s13023-014-0183-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9 (1), pp.183. 〈10.1186/s13023-014-0183-8〉
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9 (1), pp.183. ⟨10.1186/s13023-014-0183-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9 (1), pp.183. 〈10.1186/s13023-014-0183-8〉
International audience; Background : The purpose of this study was to describe the natural history of severe congenital neutropenia (SCN) in 14 patients with G6PC3 mutations and enrolled in the French SCN registry.Methods : Among 605 patients include