Resultats de la cerca - Pellier, Isabelle

MON-098 Risk of Long-Term Endocrine Sequelae in Survivors of Progressing Childhood Optic Pathway Glioma Treated by Upfront Chemotherapy: Preliminary Analyses of 102 Subjects from t... per Hippolyte, Helene, De Carli, Emilie, Pellier, Isabelle, Rialland, Xavier, Coutant, Regis

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Long-term visual acuity in patients with optic pathway glioma treated during childhood with up-front BB-SFOP chemotherapy—Analysis of a French pediatric historical cohort per Rakotonjanahary, Josué, Gravier, Nicolas, Lambron, Julien, De Carli, Emilie, Toulgoat, Frédérique, Delion, Matthieu, Pellier, Isabelle, Rialland, Xavier

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HGG-40. EXCEPTIONAL SYNCHRONOUS OCCURENCE OF A BRAF V600E MUTANT GLIOBLASTOMA AND A H3.3K27M MUTANT DIFFUSE INTRINSIC PONTINE GLIOMA: A CASE REPORT per De Carli, Emilie, Boisselier, Blandine, Fournier, Luc Le, Supiot, Stéphane, Mallebranche, Coralie, Proust-Houdemont, Stéphanie, Duplan, Mylène, Pellier, Isabelle, Rousseau, Audrey

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A cohort of French pediatric patients with primary immunodeficiencies: are patient preferences regarding replacement immunotherapy fulfilled in real-life conditions? per Pasquet, Marlène, Pellier, Isabelle, Aladjidi, Nathalie, Auvrignon, Anne, Cherin, Patrick, Clerson, Pierre, Cozon, Gregoire Jacques Noël, Jaussaud, Roland, Bienvenu, Boris, Hoarau, Cyrille

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Depicting the genetic architecture of pediatric cancers through an integrative gene network approach per Savary, Clara, Kim, Artem, Lespagnol, Alexandra, Gandemer, Virginie, Pellier, Isabelle, Andrieu, Charlotte, Pagès, Gilles, Galibert, Marie-Dominique, Blum, Yuna, de Tayrac, Marie

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Evaluation of health related quality of life in children with immune thrombocytopenia with the PedsQL™ 4.0 Generic Core Scales: a study on behalf of the pays de Loire pediatric hem... per Strullu, Marion, Rakotonjanahary, Josué, Tarral, Eliane, Savagner, Christophe, Thomas, Caroline, Méchinaud, Françoise, Reguerre, Yves, Poignant, Sylvaine, Boutet, Arnaud, Bassil, Joachim, Médinger, Dominique, Quemener, Emmanuel, Young, Nancy L, Rachieru, Petronela, Klaassen, Robert J, Pellier, Isabelle

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French “real life” experience of clofarabine in children with refractory or relapsed acute lymphoblastic leukaemia per Trioche, Pascale, Nelken, Brigitte, Michel, Gérard, Pellier, Isabelle, Petit, Arnaud, Bertrand, Yves, Rohrlich, Pierre, Schmitt, Claudine, Sirvent, Nicolas, Boutard, Patrick, Margueritte, Geneviève, Pautard, Brigitte, Ducassou, Stéphane, Plantaz, Dominique, Robert, Alain, Thomas, Caroline, Desseaux, Kristell, Chevret, Sylvie, Baruchel, André

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Persistent osteoarticular pain in children: early clinical and laboratory findings suggestive of acute lymphoblastic leukemia (a multicenter case-control study of 147 patients) per Louvigné, Mathilde, Rakotonjanahary, Josué, Goumy, Laurence, Tavenard, Aude, Brasme, Jean-François, Rialland, Fanny, Baruchel, André, Auclerc, Marie-Françoise, Despert, Véronique, Desgranges, Marie, Jean, Sylvie, Faye, Albert, Meinzer, Ulrich, Lorrot, Mathie, Job-Deslandre, Chantal, Bader-Meunier, Brigitte, Gandemer, Virginie, Pellier, Isabelle

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Hydroxychloroquine in mild-to-moderate coronavirus disease 2019: a placebo-controlled double blind trial per Dubée, Vincent, Roy, Pierre-Marie, Vielle, Bruno, Parot-Schinkel, Elsa, Blanchet, Odile, Darsonval, Astrid, Lefeuvre, Caroline, Abbara, Chadi, Boucher, Sophie, Devaud, Edouard, Robineau, Olivier, Rispal, Patrick, Guimard, Thomas, d’Anglejean, Emma, Diamantis, Sylvain, Custaud, Marc-Antoine, Pellier, Isabelle, Mercat, Alain

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Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry per Desplantes, Claire, Fremond, Marie Louise, Beaupain, Blandine, Harousseau, Jean Luc, Buzyn, Agnès, Pellier, Isabelle, Roques, Gaelle, Morville, Pierre, Paillard, Catherine, Bruneau, Julie, Pinson, Lucile, Jeziorski, Eric, Vannier, Jean Pierre, Picard, Capucine, Bellanger, Florence, Romero, Norma, de Pontual, Loïc, Lapillonne, Hélène, Lutz, Patrick, Chantelot, Christine Bellanné, Donadieu, Jean

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Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infection per Fournier, Benjamin, Boutboul, David, Bruneau, Julie, Miot, Charline, Boulanger, Cécile, Malphettes, Marion, Pellier, Isabelle, Dunogué, Bertrand, Terrier, Benjamin, Suarez, Felipe, Blanche, Stéphane, Castelle, Martin, Winter, Sarah, Delecluse, Henri-Jacques, Molina, Thierry, Picard, Capucine, Ehl, Stephan, Moshous, Despina, Galicier, Lionel, Barlogis, Vincent, Fischer, Alain, Neven, Bénédicte, Latour, Sylvain

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A novel syndrome with congenital neutropenia caused by mutations in G6PC3 per Boztug, Kaan, Appaswamy, Giridharan, Ashikov, Angel, Schäffer, Alejandro A., Salzer, Ulrich, Diestelhorst, Jana, Germeshausen, Manuela, Brandes, Gudrun, Lee-Gossler, Jacqueline, Noyan, Fatih, Gatzke, Anna-Katherina, Minkov, Milen, Greil, Johann, Kratz, Christian, Petropoulou, Theoni, Pellier, Isabelle, Bellanné-Chantelot, Christine, Rezaei, Nima, Mönkemöller, Kirsten, Irani-Hakimeh, Noha, Bakker, Hans, Gerardy-Schahn, Rita, Zeidler, Cornelia, Grimbacher, Bodo, Welte, Karl, Klein, Christoph

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Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort per Aladjidi, Nathalie, Fernandes, Helder, Leblanc, Thierry, Vareliette, Amélie, Rieux-Laucat, Frédéric, Bertrand, Yves, Chambost, Hervé, Pasquet, Marlène, Mazingue, Françoise, Guitton, Corinne, Pellier, Isabelle, Roqueplan-Bellmann, Françoise, Armari-Alla, Corinne, Thomas, Caroline, Marie-Cardine, Aude, Lejars, Odile, Fouyssac, Fanny, Bayart, Sophie, Lutz, Patrick, Piguet, Christophe, Jeziorski, Eric, Rohrlich, Pierre, Lemoine, Philippe, Bodet, Damien, Paillard, Catherine, Couillault, Gérard, Millot, Frédéric, Fischer, Alain, Pérel, Yves, Leverger, Guy

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Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden per Pincez, Thomas, Fernandes, Helder, Leblanc, Thierry, Michel, Gérard, Barlogis, Vincent, Bertrand, Yves, Neven, Bénédicte, Chahla, Wadih Abou, Pasquet, Marlène, Guitton, Corinne, Marie-Cardine, Aude, Pellier, Isabelle, Armari-Alla, Corinne, Benadiba, Joy, Blouin, Pascale, Jeziorski, Eric, Millot, Frédéric, Paillard, Catherine, Thomas, Caroline, Cheikh, Nathalie, Bayart, Sophie, Fouyssac, Fanny, Piguet, Christophe, Deparis, Marianna, Briandet, Claire, Doré, Eric, Picard, Capucine, Rieux-Laucat, Frédéric, Landman-Parker, Judith, Leverger, Guy, Aladjidi, Nathalie

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Invasive Pneumococcal Disease in Children Can Reveal a Primary Immunodeficiency per Gaschignard, Jean, Levy, Corinne, Chrabieh, Maya, Boisson, Bertrand, Bost-Bru, Cécile, Dauger, Stéphane, Dubos, François, Durand, Philippe, Gaudelus, Joël, Gendrel, Dominique, Gras Le Guen, Christèle, Grimprel, Emmanuel, Guyon, Gaël, Jeudy, Catherine, Jeziorski, Eric, Leclerc, Francis, Léger, Pierre-Louis, Lesage, Fabrice, Lorrot, Mathie, Pellier, Isabelle, Pinquier, Didier, de Pontual, Loïc, Sachs, Philippe, Thomas, Caroline, Tissières, Pierre, Valla, Frédéric V., Desprez, Philippe, Frémeaux-Bacchi, Véronique, Varon, Emmanuelle, Bossuyt, Xavier, Cohen, Robert, Abel, Laurent, Casanova, Jean-Laurent, Puel, Anne, Picard, Capucine

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Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency per Ciancanelli, Michael J., Huang, Sarah X. L., Luthra, Priya, Garner, Hannah, Itan, Yuval, Volpi, Stefano, Lafaille, Fabien G., Trouillet, Céline, Schmolke, Mirco, Albrecht, Randy A., Israelsson, Elisabeth, Lim, Hye Kyung, Casadio, Melina, Hermesh, Tamar, Lorenzo, Lazaro, Leung, Lawrence W., Pedergnana, Vincent, Boisson, Bertrand, Okada, Satoshi, Picard, Capucine, Ringuier, Benedicte, Troussier, Françoise, Chaussabel, Damien, Abel, Laurent, Pellier, Isabelle, Notarangelo, Luigi D., García-Sastre, Adolfo, Basler, Christopher F., Geissmann, Frédéric, Zhang, Shen-Ying, Snoeck, Hans-Willem, Casanova, Jean-Laurent

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Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome per Bellanné-Chantelot, Christine, Schmaltz-Panneau, Barbara, Marty, Caroline, Fenneteau, Odile, Callebaut, Isabelle, Clauin, Séverine, Docet, Aurélie, Damaj, Gandhi-Laurent, Leblanc, Thierry, Pellier, Isabelle, Stoven, Cécile, Souquere, Sylvie, Antony-Debré, Iléana, Beaupain, Blandine, Aladjidi, Nathalie, Barlogis, Vincent, Bauduer, Frédéric, Bensaid, Philippe, Boespflug-Tanguy, Odile, Berger, Claire, Bertrand, Yves, Carausu, Liana, Fieschi, Claire, Galambrun, Claire, Schmidt, Aline, Journel, Hubert, Mazingue, Françoise, Nelken, Brigitte, Quah, Thuan Chong, Oksenhendler, Eric, Ouachée, Marie, Pasquet, Marlène, Saada, Véronique, Suarez, Felipe, Pierron, Gérard, Vainchenker, William, Plo, Isabelle, Donadieu, Jean

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Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency per Campbell, Tessa Mollie, Liu, Zhiyong, Zhang, Qian, Moncada-Velez, Marcela, Covill, Laura E., Zhang, Peng, Alavi Darazam, Ilad, Bastard, Paul, Bizien, Lucy, Bucciol, Giorgia, Lind Enoksson, Sara, Jouanguy, Emmanuelle, Karabela, Şemsi Nur, Khan, Taushif, Kendir-Demirkol, Yasemin, Arias, Andres Augusto, Mansouri, Davood, Marits, Per, Marr, Nico, Migeotte, Isabelle, Moens, Leen, Ozcelik, Tayfun, Pellier, Isabelle, Sendel, Anton, Şenoğlu, Sevtap, Shahrooei, Mohammad, Smith, C.I. Edvard, Vandernoot, Isabelle, Willekens, Karen, Kart Yaşar, Kadriye, Bergman, Peter, Abel, Laurent, Cobat, Aurélie, Casanova, Jean-Laurent, Meyts, Isabelle, Bryceson, Yenan T.

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Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage per Angulo, Ivan, Vadas, Oscar, Garçon, Fabien, Banham-Hall, Edward, Plagnol, Vincent, Leahy, Timothy R., Baxendale, Helen, Coulter, Tanya, Curtis, James, Wu, Changxin, Blake-Palmer, Katherine, Perisic, Olga, Smyth, Deborah, Maes, Mailis, Fiddler, Christine, Juss, Jatinder, Cilliers, Deirdre, Markelj, Gašper, Chandra, Anita, Farmer, George, Kielkowska, Anna, Clark, Jonathan, Kracker, Sven, Debré, Marianne, Picard, Capucine, Pellier, Isabelle, Jabado, Nada, Morris, James A., Barcenas-Morales, Gabriela, Fischer, Alain, Stephens, Len, Hawkins, Phillip, Barrett, Jeffrey C., Abinun, Mario, Clatworthy, Menna, Durandy, Anne, Doffinger, Rainer, Chilvers, Edwin, Cant, Andrew J., Kumararatne, Dinakantha, Okkenhaug, Klaus, Williams, Roger L., Condliffe, Alison, Nejentsev, Sergey

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BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy per Héritier, Sébastien, Emile, Jean-François, Barkaoui, Mohamed-Aziz, Thomas, Caroline, Fraitag, Sylvie, Boudjemaa, Sabah, Renaud, Florence, Moreau, Anne, Peuchmaur, Michel, Chassagne-Clément, Catherine, Dijoud, Frédérique, Rigau, Valérie, Moshous, Despina, Lambilliotte, Anne, Mazingue, Françoise, Kebaili, Kamila, Miron, Jean, Jeziorski, Eric, Plat, Geneviève, Aladjidi, Nathalie, Ferster, Alina, Pacquement, Hélène, Galambrun, Claire, Brugières, Laurence, Leverger, Guy, Mansuy, Ludovic, Paillard, Catherine, Deville, Anne, Armari-Alla, Corinne, Lutun, Anne, Gillibert-Yvert, Marion, Stephan, Jean-Louis, Cohen-Aubart, Fleur, Haroche, Julien, Pellier, Isabelle, Millot, Frédéric, Lescoeur, Brigitte, Gandemer, Virginie, Bodemer, Christine, Lacave, Roger, Hélias-Rodzewicz, Zofia, Taly, Valérie, Geissmann, Frédéric, Donadieu, Jean

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