Early treatment of neonatal diabetes with oral glibenclamide in an extremely preterm infant von Galderisi, Alfonso, Kermorvant‐Duchemin, Elsa, Daruich, Alejandra, Bonnard, Adeline Alice, Lapillonne, Alexandre, Aubelle, Marie‐Stéphanie, Perrella, Bruna, Vial, Yoann, Cave, Héléne, Berdugo, Marianne, Jarreau, Pierre‐Henri, Polak, Michel, Beltrand, Jacques

Volltext

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients von Donadieu, Jean, Lamant, Marie, Fieschi, Claire, de Fontbrune, Flore Sicre, Caye, Aurélie, Ouachee, Marie, Beaupain, Blandine, Bustamante, Jacinta, Poirel, Hélène A, Isidor, Bertrand, Van Den Neste, Eric, Neel, Antoine, Nimubona, Stanislas, Toutain, Fabienne, Barlogis, Vincent, Schleinitz, Nicolas, Leblanc, Thierry, Rohrlich, Pierre, Suarez, Felipe, Ranta, Dana, Chahla, Wadih Abou, Bruno, Bénédicte, Terriou, Louis, Francois, Sylvie, Lioure, Bruno, Ahle, Guido, Bachelerie, Françoise, Preudhomme, Claude, Delabesse, Eric, Cave, Hélène, Bellanné-Chantelot, Christine, Pasquet, Marlène

Volltext

Efficacy of tyrosine kinase inhibitors in Ph-like acute lymphoblastic leukemia harboring ABL-class rearrangements von Tanasi, Ilaria, Ba, Ibrahima, Sirvent, Nicolas, Braun, Thorsten, Cuccuini, Wendy, Ballerini, Paola, Duployez, Nicolas, Tanguy-Schmidt, Aline, Tamburini, Jérôme, Maury, Sébastien, Doré, Eric, Himberlin, Chantal, Duclos, Cédric, Chevallier, Patrice, Rousselot, Philippe, Bonifacio, Massimiliano, Cavé, Hélène, Baruchel, André, Dombret, Hervé, Soulier, Jean, Landman-Parker, Judith, Boissel, Nicolas, Clappier, Emmanuelle

Volltext

Favorable outcome of NUTM1-rearranged infant and pediatric B cell precursor acute lymphoblastic leukemia in a collaborative international study von Boer, Judith M., Valsecchi, Maria Grazia, Hormann, Femke M., Antić, Željko, Zaliova, Marketa, Schwab, Claire, Cazzaniga, Giovanni, Arfeuille, Chloé, Cavé, Hélène, Attarbaschi, Andishe, Strehl, Sabine, Escherich, Gabriele, Imamura, Toshihiko, Ohki, Kentaro, Grüber, Tanja A., Sutton, Rosemary, Pastorczak, Agata, Lammens, Tim, Lambert, Frédéric, Li, Chi Kong, Carrillo de Santa Pau, Enrique, Hoffmann, Steve, Möricke, Anja, Harrison, Christine J., Den Boer, Monique L., De Lorenzo, Paola, Stam, Ronald W., Bergmann, Anke K., Pieters, Rob

Volltext

Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome von Cordeddu, Viviana, Yin, Jiani C., Gunnarsson, Cecilia, Virtanen, Carl, Drunat, Séverine, Lepri, Francesca, De Luca, Alessandro, Rossi, Cesare, Ciolfi, Andrea, Pugh, Trevor J., Bruselles, Alessandro, Priest, James R., Pennacchio, Len A., Lu, Zhibin, Danesh, Arnavaz, Quevedo, Rene, Hamid, Alaa, Martinelli, Simone, Pantaleoni, Francesca, Gnazzo, Maria, Daniele, Paola, Lissewski, Christina, Bocchinfuso, Gianfranco, Stella, Lorenzo, Odent, Sylvie, Philip, Nicole, Faivre, Laurence, Vlckova, Marketa, Seemanova, Eva, Digilio, Cristina, Zenker, Martin, Zampino, Giuseppe, Verloes, Alain, Dallapiccola, Bruno, Roberts, Amy E., Cavé, Hélène, Gelb, Bruce D., Neel, Benjamin G., Tartaglia, Marco

Volltext

Clinical characteristics and outcomes of B-ALL with ZNF384 rearrangements: a retrospective analysis by the Ponte di Legno Childhood ALL Working Group von Hirabayashi, Shinsuke, Butler, Ellie R., Ohki, Kentaro, Kiyokawa, Nobutaka, Bergmann, Anke K., Möricke, Anja, Boer, Judith M., Cavé, Hélène, Cazzaniga, Giovanni, Yeoh, Allen Eng Juh, Sanada, Masashi, Imamura, Toshihiko, Inaba, Hiroto, Mullighan, Charles, Loh, Mignon L., Norén-Nyström, Ulrika, Pastorczak, Agata, Shih, Lee-Yung, Zaliova, Marketa, Pui, Ching-Hon, Haas, Oskar A., Harrison, Christine J., Moorman, Anthony V., Manabe, Atsushi

Volltext

Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications von Lissewski, Christina, Chune, Valérie, Pantaleoni, Francesca, De Luca, Alessandro, Capri, Yline, Brinkmann, Julia, Lepri, Francesca, Daniele, Paola, Leenders, Erika, Mazzanti, Laura, Scarano, Emanuela, Radio, Francesca Clementina, Kutsche, Kerstin, Kuechler, Alma, Gérard, Marion, Ranguin, Kara, Legendre, Marine, Vial, Yoann, van der Burgt, Ineke, Rinne, Tuula, Andreucci, Elena, Mastromoro, Gioia, Digilio, Maria Cristina, Cave, Hélène, Tartaglia, Marco, Zenker, Martin

Volltext

Determinants of CD19-positive vs CD19-negative relapse after tisagenlecleucel for B-cell acute lymphoblastic leukemia von Dourthe, Marie-Emilie, Rabian, Florence, Yakouben, Karima, Chevillon, Florian, Cabannes-Hamy, Aurélie, Méchinaud, Françoise, Grain, Audrey, Chaillou, Delphine, Rahal, Ilhem, Caillat-Zucman, Sophie, Lesprit, Emmanuelle, Naudin, Jérôme, Roupret-Serzec, Julie, Parquet, Nathalie, Brignier, Anne, Guérin-El Khourouj, Valérie, Lainey, Elodie, Caye-Eude, Aurélie, Cavé, Hélène, Clappier, Emmanuelle, Mathis, Stéphanie, Azoulay, Elie, Dalle, Jean Hugues, Dhédin, Nathalie, Madelaine, Isabelle, Larghero, Jérôme, Boissel, Nicolas, Baruchel, André

Volltext

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome von Capri, Yline, Flex, Elisabetta, Krumbach, Oliver H.F., Carpentieri, Giovanna, Cecchetti, Serena, Lißewski, Christina, Rezaei Adariani, Soheila, Schanze, Denny, Brinkmann, Julia, Piard, Juliette, Pantaleoni, Francesca, Lepri, Francesca R., Goh, Elaine Suk-Ying, Chong, Karen, Stieglitz, Elliot, Meyer, Julia, Kuechler, Alma, Bramswig, Nuria C., Sacharow, Stephanie, Strullu, Marion, Vial, Yoann, Vignal, Cédric, Kensah, George, Cuturilo, Goran, Kazemein Jasemi, Neda S., Dvorsky, Radovan, Monaghan, Kristin G., Vincent, Lisa M., Cavé, Hélène, Verloes, Alain, Ahmadian, Mohammad R., Tartaglia, Marco, Zenker, Martin

Volltext

Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature von Siegfried, Aurore, Cances, Claude, Denuelle, Marie, Loukh, Najat, Tauber, Maïté, Cavé, Hélène, Delisle, Marie‐Bernadette

Volltext

Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL–USP2 fusions von Meyer, Claus, Lopes, Bruno A., Caye-Eude, Aurélie, Cavé, Hélène, Arfeuille, Chloé, Cuccuini, Wendy, Sutton, Rosemary, Venn, Nicola C., Oh, Seung Hwan, Tsaur, Grigory, Escherich, Gabriele, Feuchtinger, Tobias, Kosasih, Hansen J., Khaw, Seong L., Ekert, Paul G., Pombo-de-Oliveira, Maria S., Bidet, Audrey, Djahanschiri, Bardya, Ebersberger, Ingo, Zaliova, Marketa, Zuna, Jan, Zermanova, Zuzana, Juvonen, Vesa, Grümayer, Renate Panzer, Fazio, Grazia, Cazzaniga, Gianni, Larghero, Patrizia, Emerenciano, Mariana, Marschalek, Rolf

Volltext

Predictive value of minimal residual disease in Philadelphia-chromosome-positive acute lymphoblastic leukemia treated with imatinib in the European intergroup study of post-inducti... von Cazzaniga, Giovanni, De Lorenzo, Paola, Alten, Julia, Röttgers, Silja, Hancock, Jeremy, Saha, Vaskar, Castor, Anders, Madsen, Hans O, Gandemer, Virginie, Cavé, Hélène, Leoni, Veronica, Köhler, Rolf, Ferrari, Giulia M, Bleckmann, Kirsten, Pieters, Rob, van der Velden, Vincent, Stary, Jan, Zuna, Jan, Escherich, Gabriele, Stadt, Udo Zur, Aricò, Maurizio, Conter, Valentino, Schrappe, Martin, Valsecchi, Maria Grazia, Biondi, Andrea

Volltext

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Dia... von Polak, Michel, Dechaume, Aurélie, Cavé, Hélène, Nimri, Revital, Crosnier, Hélène, Sulmont, Véronique, de Kerdanet, Marc, Scharfmann, Raphael, Lebenthal, Yael, Froguel, Philippe, Vaxillaire, Martine

Volltext

The polymerase chain reaction, so simple, so clever: the discovery that made minimal residual disease come true von Cavé, Hélène

Volltext

Acute lymphoblastic leukemia in children with Down syndrome: a retrospective analysis from the Ponte di Legno study group von Buitenkamp, Trudy D., Izraeli, Shai, Zimmermann, Martin, Forestier, Erik, Heerema, Nyla A., van den Heuvel-Eibrink, Marry M., Pieters, Rob, Korbijn, Carin M., Silverman, Lewis B., Schmiegelow, Kjeld, Liang, Der-Cheng, Horibe, Keizo, Arico, Maurizio, Biondi, Andrea, Basso, Giuseppe, Rabin, Karin R., Schrappe, Martin, Cario, Gunnar, Mann, Georg, Morak, Maria, Panzer-Grümayer, Renate, Mondelaers, Veerle, Lammens, Tim, Cavé, Hélène, Stark, Batia, Ganmore, Ithamar, Moorman, Anthony V., Vora, Ajay, Hunger, Stephen P., Pui, Ching-Hon, Mullighan, Charles G., Manabe, Atsushi, Escherich, Gabriele, Kowalczyk, Jerzy R., Whitlock, James A., Zwaan, C. Michel

Volltext

Germline bi-allelic SH2B3/LNK alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder von Arfeuille, Chloé, Vial, Yoann, Cadenet, Margaux, Caye-Eude, Aurélie, Fenneteau, Odile, Neven, Quentin, Bonnard, Adeline A, Pizzi, Simone, Carpentieri, Giovanna, Capri, Yline, Girardi, Katia, Pedace, Lucia, Macchiaiolo, Marina, Boudhar, Kamel, Khaled, Monia Ben, Chahla, Wadih Abou, Lutun, Anne, Fahd, Mony, Drunat, Séverine, Flex, Elisabetta, Dalle, Jean-Hugues, Strullu, Marion, Locatelli, Franco, Tartaglia, Marco, Cavé, Hélène

Volltext

Differential activation of basal and IL-7-induced PI3K/Akt/ mTOR and JAK/STAT5 signaling distinguishes pediatric from adult acute lymphoblastic leukemia von Fernandes, Marta B, Gomes, A Margarida, Oliveira, Mariana L, Caldas, Joana, Lúcio, Paulo, Kim, Rathana, Caye-Eude, Aurélie, Pereira, Filomena, De Sousa, Aida B, De Stefano, Alessia, Follo, Matilde Y, Soares, Maria V, Lacerda, João F, Desterro, Joana, Cavé, Hélène, Clappier, Emmanuelle, Duarte, Ximo, Ribeiro, Patrícia, Barata, João T

Volltext

LIN28B overexpression defines a novel fetal-like subgroup of juvenile myelomonocytic leukemia von Helsmoortel, Hetty H., Bresolin, Silvia, Lammens, Tim, Cavé, Hélène, Noellke, Peter, Caye, Aurélie, Ghazavi, Farzaneh, de Vries, Andrica, Hasle, Henrik, Labarque, Veerle, Masetti, Riccardo, Stary, Jan, van den Heuvel-Eibrink, Marry M., Philippé, Jan, Van Roy, Nadine, Benoit, Yves, Speleman, Frank, Niemeyer, Charlotte, Flotho, Christian, Basso, Giuseppe, te Kronnie, Geertruy, Van Vlierberghe, Pieter, De Moerloose, Barbara

Volltext

Dexamethasone (6 mg/m2/day) and prednisolone (60 mg/m2/day) were equally effective as induction therapy for childhood acute lymphoblastic leukemia in the EORTC CLG 58951 randomized... von Domenech, Carine, Suciu, Stefan, De Moerloose, Barbara, Mazingue, Françoise, Plat, Geneviève, Ferster, Alina, Uyttebroeck, Anne, Sirvent, Nicolas, Lutz, Patrick, Yakouben, Karima, Munzer, Martine, Röhrlich, Pierre, Plantaz, Dominique, Millot, Frederic, Philippet, Pierre, Dastugue, Nicole, Girard, Sandrine, Cavé, Hélène, Benoit, Yves, Bertrandfor, Yves

Volltext

Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic Leukemia von Mulero-Navarro, Sonia, Sevilla, Ana, Roman, Angel C., Lee, Dung-Fang, D’Souza, Sunita L., Pardo, Sherly, Riess, Ilan, Su, Jie, Cohen, Ninette, Schaniel, Christoph, Rodriguez, Nelson A., Baccarini, Alessia, Brown, Brian D., Cavé, Hélène, Caye, Aurélie, Strullu, Marion, Yalcin, Safak, Park, Christopher Y., Dhandapany, Perundurai S., Yongchao, Ge, Edelmann, Lisa, Bahieg, Sawsan, Raynal, Patrick, Flex, Elisabetta, Tartaglia, Marco, Moore, Kateri A., Lemischka, Ihor R., Gelb, Bruce D.

Volltext