Respiratory distress and sudden death of a patient with GSDIb chronic neutropenia: possible role of pegfilgrastim

Por Donadieu, Jean, Beaupain, Blandine, Rety-Jacob, Frédérique, Nove-Josserand, Raphaelle
Publicado em 2009

Congenital neutropenia: diagnosis, molecular bases and patient management

Por Donadieu, Jean, Fenneteau, Odile, Beaupain, Blandine, Mahlaoui, Nizar, Chantelot, Christine Bellanné
Publicado em 2011

Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5

Por Duan, Zhijun, Person, Richard E., Lee, Hu-Hui, Huang, Shi, Donadieu, Jean, Badolato, Raffaele, Grimes, H. Leighton, Papayannopoulou, Thalia, Horwitz, Marshall S.
Publicado em 2007

Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome

Por Badolato, Raffaele, Dotta, Laura, Tassone, Laura, Amendola, Giovanni, Porta, Fulvio, Locatelli, Franco, Notarangelo, Lucia D., Bertrand, Yves, Bachelerie, Francoise, Donadieu, Jean
Publicado em 2012

Analysis of a French cohort of patients with large granular lymphocyte leukemia: a report on 229 cases

Por Bareau, Benoît, Rey, Jérôme, Hamidou, Mohamed, Donadieu, Jean, Morcet, Jeff, Reman, Oumedaly, Schleinitz, Nicolas, Tournilhac, Olivier, Roussel, Mikael, Fest, Thierry, Lamy, Thierry
Publicado em 2010

B-RAF Mutant Alleles Associated with Langerhans Cell Histiocytosis, a Granulomatous Pediatric Disease

Por Satoh, Takeshi, Smith, Alexander, Sarde, Aurelien, Lu, Hui-chun, Mian, Sophie, Trouillet, Celine, Mufti, Ghulam, Emile, Jean-Francois, Fraternali, Franca, Donadieu, Jean, Geissmann, Frederic
Publicado em 2012

Correction: B-RAF Mutant Alleles Associated with Langerhans Cell Histiocytosis, a Granulomatous Pediatric Disease

Por Satoh, Takeshi, Smith, Alexander, Sarde, Aurelien, Lu, Hui-chun, Mian, Sophie, Trouillet, Celine, Mufti, Ghulam, Emile, Jean-Francois, Fraternali, Franca, Donadieu, Jean, Geissmann, Frederic
Publicado em 2012

Langerhans Cell Histiocytosis (LCH): Guidelines for Diagnosis, Clinical Work-Up, and Treatment for Patients Till the Age of 18 Years

Por Haupt, Riccardo, Minkov, Milen, Astigarraga, Itziar, Schäfer, Eva, Nanduri, Vasanta, Jubran, Rima, Egeler, R Maarten, Janka, Gritta, Micic, Dragan, Rodriguez-Galindo, Carlos, Van Gool, Stefaan, Visser, Johannes, Weitzman, Sheila, Donadieu, Jean
Publicado no Pediatr Blood Cancer (2013)

Neutropenia-associated ELANE mutations disrupting translation initiation produce novel neutrophil elastase isoforms

Por Tidwell, Timothy, Wechsler, Jeremy, Nayak, Ramesh C., Trump, Lisa, Salipante, Stephen J., Cheng, Jerry C., Donadieu, Jean, Glaubach, Taly, Corey, Seth J., Grimes, H. Leighton, Lutzko, Carolyn, Cancelas, Jose A., Horwitz, Marshall S.
Publicado em 2014

Herpes-Virus Infection in Patients with Langerhans Cell Histiocytosis: A Case-Controlled Sero-Epidemiological Study, and In Situ Analysis

Por Jeziorski, Eric, Senechal, Brigitte, Molina, Thierry Jo, Devez, Francis, Leruez-Ville, Marianne, Morand, Patrice, Glorion, Christophe, Mansuy, Ludovic, Gaudelus, Joel, Debre, Marianne, Jaubert, Francis, Seigneurin, Jean-Marie, Thomas, Caroline, Joab, Irene, Donadieu, Jean, Geissmann, Frederic
Publicado em 2008

Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis

Por Jaeger, Baptiste N., Donadieu, Jean, Cognet, Céline, Bernat, Claire, Ordoñez-Rueda, Diana, Barlogis, Vincent, Mahlaoui, Nizar, Fenis, Aurore, Narni-Mancinelli, Emilie, Beaupain, Blandine, Bellanné-Chantelot, Christine, Bajénoff, Marc, Malissen, Bernard, Malissen, Marie, Vivier, Eric, Ugolini, Sophie
Publicado em 2012

Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study

Por Donadieu, Jean, Bernard, Frederic, van Noesel, Max, Barkaoui, Mohamed, Bardet, Odile, Mura, Rosella, Arico, Maurizio, Piguet, Christophe, Gandemer, Virginie, Armari Alla, Corinne, Clausen, Niels, Jeziorski, Eric, Lambilliote, Anne, Weitzman, Sheila, Henter, Jan Inge, Van Den Bos, Cor
Publicado no Blood (2015)

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome

Por Donadieu, Jean, Fenneteau, Odile, Beaupain, Blandine, Beaufils, Sandrine, Bellanger, Florence, Mahlaoui, Nizar, Lambilliotte, Anne, Aladjidi, Nathalie, Bertrand, Yves, Mialou, Valérie, Perot, Christine, Michel, Gérard, Fouyssac, Fanny, Paillard, Catherine, Gandemer, Virginie, Boutard, Patrick, Schmitz, Jacques, Morali, Alain, Leblanc, Thierry, Bellanné-Chantelot, Christine
Publicado em 2012

Expansion of Regulatory T Cells in Patients with Langerhans Cell Histiocytosis

Por Senechal, Brigitte, Elain, Gaelle, Jeziorski, Eric, Grondin, Virginie, Patey-Mariaud de Serre, Natacha, Jaubert, Francis, Beldjord, Kheira, Lellouch, Arielle, Glorion, Christophe, Zerah, Michel, Mary, Pierre, Barkaoui, Mohammed, Emile, Jean Francois, Boccon-Gibod, Liliane, Josset, Patrice, Debré, Marianne, Fischer, Alain, Donadieu, Jean, Geissmann, Frederic
Publicado em 2007

Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Por Thuret, Isabelle, Pondarré, Corinne, Loundou, Anderson, Steschenko, Dominique, Girot, Robert, Bachir, Dora, Rose, Christian, Barlogis, Vincent, Donadieu, Jean, de Montalembert, Mariane, Hagege, Isabelle, Pegourie, Brigitte, Berger, Claire, Micheau, Marguerite, Bernaudin, Françoise, Leblanc, Thierry, Lutz, Laurence, Galactéros, Frédéric, Siméoni, Marie-Claude, Badens, Catherine
Publicado em 2010

Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

Por Beaussant Cohen, Sarah, Fenneteau, Odile, Plouvier, Emmanuel, Rohrlich, Pierre-Simon, Daltroff, Gerard, Plantier, Isabelle, Dupuy, Alain, Kerob, Delphine, Beaupain, Blandine, Bordigoni, Pierre, Fouyssac, Fanny, Delezoide, Anne-Lise, Devouassoux, Gilles, Nicolas, Jean François, Bensaid, Philippe, Bertrand, Yves, Balabanian, Karl, Chantelot, Christine Bellanne, Bachelerie, Françoise, Donadieu, Jean
Publicado em 2012

Natural history of Barth syndrome: a national cohort study of 22 patients

Por Rigaud, Charlotte, Lebre, Anne-Sophie, Touraine, Renaud, Beaupain, Blandine, Ottolenghi, Chris, Chabli, Allel, Ansquer, Helene, Ozsahin, Hulya, Di Filippo, Sylvie, De Lonlay, Pascale, Borm, Betina, Rivier, Francois, Vaillant, Marie-Catherine, Mathieu-Dramard, Michèle, Goldenberg, Alice, Viot, Géraldine, Charron, Philippe, Rio, Marlene, Bonnet, Damien, Donadieu, Jean
Publicado em 2013

Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome

Por Finch, Andrew J., Hilcenko, Christine, Basse, Nicolas, Drynan, Lesley F., Goyenechea, Beatriz, Menne, Tobias F., González Fernández, África, Simpson, Paul, D'Santos, Clive S., Arends, Mark J., Donadieu, Jean, Bellanné-Chantelot, Christine, Costanzo, Michael, Boone, Charles, McKenzie, Andrew N., Freund, Stefan M.V., Warren, Alan J.
Publicado em 2011

Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry

Por 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
Publicado no Orphanet J Rare Dis (2014)

High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia

Por Pasquet, Marlène, Bellanné-Chantelot, Christine, Tavitian, Suzanne, Prade, Naïs, Beaupain, Blandine, LaRochelle, Olivier, Petit, Arnaud, Rohrlich, Pierre, Ferrand, Christophe, Van Den Neste, Eric, Poirel, Hélène A., Lamy, Thierry, Ouachée-Chardin, Marie, Mansat-De Mas, Véronique, Corre, Jill, Récher, Christian, Plat, Geneviève, Bachelerie, Françoise, Donadieu, Jean, Delabesse, Eric
Publicado em 2013