Search Results - 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... by 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 by 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 by 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? by 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 by 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... by 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 by 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) by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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