Anomalías morfológicas de los leucocitos en el niño von O Fenneteau

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An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions von Clappier, E, Auclerc, M-F, Rapion, J, Bakkus, M, Caye, A, Khemiri, A, Giroux, C, Hernandez, L, Kabongo, E, Savola, S, Leblanc, T, Yakouben, K, Plat, G, Costa, V, Ferster, A, Girard, S, Fenneteau, O, Cayuela, J-M, Sigaux, F, Dastugue, N, Suciu, S, Benoit, Y, Bertrand, Y, Soulier, J, Cavé, H

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New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte Dehydration von Allegrini, B., Jedele, S., David Nguyen, L., Mignotet, M., Rapetti-Mauss, R., Etchebest, C., Fenneteau, O., Loubat, A., Boutet, A., Thomas, C., Durin, J., Petit, A., Badens, C., Garçon, L., Da Costa, L., Guizouarn, H.

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Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia von Pérez, B, Mechinaud, F, Galambrun, C, Ben Romdhane, N, Isidor, B, Philip, N, Derain-Court, J, Cassinat, B, Lachenaud, J, Kaltenbach, S, Salmon, A, Désirée, C, Pereira, S, Menot, M L, Royer, N, Fenneteau, O, Baruchel, A, Chomienne, C, Verloes, A, Cavé, H

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Performance evaluation of the Sysmex XN-1000 hematology analyzer in assessment of the white blood cell count differential in pediatric specimens von Becker, P.-H., Fenneteau, O., Da Costa, L.

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In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia von Strullu, M, Caye, A, Cassinat, B, Fenneteau, O, Touzot, F, Blauwblomme, T, Rodriguez, R, Latour, S, Petit, A, Barlogis, V, Galambrun, C, Leblanc, T, Baruchel, A, Chomienne, C, Cavé, H

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Is Acute Myeloblastic Leukemia in Children Under 2 Years of Age a Specific Entity? A Report from the FRENCH ELAM02 Study Group von Blais, S., Boutroux, H., Pasquet, M., Leblanc, T., Fenneteau, O., Gandemer, V., Bertrand, Y., Ducassou, S., Michel, G., Nelken, B., Petit, A., Cuccuini, W., Gouache, E., Renaut, Marceau‐A., Baruchel, A., Lapillonne, H., Leverger, G.

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Exploration d’une macrocytose : le point de vue du cytologiste von Lainey, E., Fenneteau, O.

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Evaluation of the CellaVision DM automated microscope in pediatrics von Billard, M, Lainey, E, Armoogum, P, Alberti, C, Fenneteau, O, Da Costa, L

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Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome von DONADIEU, Jean, FENNETEAU, Odile, PEROT, Christine, MICHEL, Gérard, FOUYSSAC, Fanny, PAILLARD, Catherine, GANDEMER, Virginie, BOUTARD, Patrick, SCHMITZ, Jacques, MORALI, Alain, LEBLANC, Thierry, BELLANNE-CHANTELOT, Christine, BEAUPAIN, Blandine, BEAUFILS, Sandrine, BELLANGER, Florence, MAHLAOUI, Nizar, LAMBILLIOTTE, Anne, ALADJIDI, Nathalie, BERTRAND, Yves, MIALOU, Valérie

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Bone marrow examination of inherited diseases in children von Fenneteau, O, Lainey, E

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Assessment of diagnostic methods for imported malaria in mainland France von Kamaliddin, C., Le Bouar, M., Berry, A., Fenneteau, O., Gillet, P., Godineau, N., Candolfi, E., Houzé, S.

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Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Stu... von Donadieu, J, Leblanc, T, Bader Meunier, B, Barkaoui, M, Fenneteau, O, Bertrand, Y, Maier-Redelsperger, M, Micheau, M, Stephan, JL, Phillipe, N, Bordigoni, P, Babin-Boilletot, A, Bensaid, P, Manel, AM, Vilmer, E, Thuret, I, Blanche, S, Gluckman, E, Fischer, A, Mechinaud, F, Joly, B, Lamy, T, Hermine, O, Cassinat, B, Bellanne-Chantelot, C, Chomienne, C, French Severe Chronic Neutropenia Study Group

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Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register von Bellanné-Chantelot, Christine, Clauin, Séverine, Leblanc, Thierry, Cassinat, Bruno, Rodrigues-Lima, Fernando, Beaufils, Sandrine, Vaury, Christelle, Barkaoui, Mohamed, Fenneteau, Odile, Maier-Redelsperger, Micheline, Chomienne, Christine, Donadieu, Jean

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Prospective Monitoring and Quantitation of Residual Blasts in Childhood Acute Lymphoblastic Leukemia by Polymerase Chain Reaction Study of δ and γ T-Cell Receptor Genes von Cavé, H., Guidal, C., Rohrlich, P., Delfau, M.H., Broyart, A., Lescoeur, B., Rahimy, C., Fenneteau, O., Monplaisir, N., d’Auriol, L., Elion, J., Vilmer, E., Grandchamp, B.

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B-Cell Acute Lymphoblastic Leukemia (B-ALL) with T (5;14)(Q31;Q32);IGH-IL3 Rearrangement and Eosinophilia: A Peculiar IGH-Rearranged B-ALL von Fournier, B., Balducci, E., Duployez, N., Clappier, E., Cuccuini, W., Cavé, H., Colomb, E. Bottollier-Lemallaz, Nebral, K., Derrieux, C., Cabannes-Hamy, A., Etancelin, P., Fenneteau, O., Gourmel, A., Loosveld, Marie, Gerard, M., Nadal, N., Reismueller, B., Attarbaschi, A., Lafage-Pochitaloff, M., Baruchel, A.

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Valeur diagnostique du myélogramme au cours des pathologies constitutionnelles de l'enfant von FENNETEAU, O, LAINEY, E

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Preferential expression of domain cassettes 4, 8 and 13 of Plasmodium falciparum erythrocyte membrane protein 1 in severe malaria imported in France von Argy, N., Bertin, G.I., Milet, J., Hubert, V., Clain, J., Cojean, S., Houzé, P., Tuikue-Ndam, N., Kendjo, E., Deloron, P., Houzé, S., Matheron, S., Casalino, E., Wolff, M., Delaval, A., Agnamey, P., Durand, R., Pilo, J.E., Rapp, C., Faucher, J.F., Cuisenier, B., Poilane, I., Bemba, D., Roide, A., Debourgogne, A., Thibault, M., Toubas, D., Patoz, P., De Gentile, L., Pons, D., Hurst, J.P., Lohmann, C., Bigel, M.L., Godineau, N., Thouvenin, M., Dunand, J., Ait-Ammar, N., Angoulvant, A., Dahane, N., Lefevre, M., Murat, J.B., Garnaud, C., Dannaoui, E., Botterel, F., Dutoit, E., Dardé, M.L., Ichou, H., Branger, C., Penn, P., Angebault, C., Morio, F., Bret, L., Thellier, M., Mouri, O., Cateau, E., Siriez, J.Y., Fenneteau, O., Revest, M., Belaz, S., Belkadi, G., Hamane, S., Bretagne, S., Aboubacar, A., Leloup, G., Develoux, M., Lapillonne, H., Eloy, O., Nevez, G., Raffenot, D., Buret, B., Desoubeaux, G., Goepp, A.

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Aspect cytologique normal et pathologique du sang chez le nouveau-né et le jeune enfant von FENNETEAU, O, HURTAUD-ROUX, M.-F, SCHLEGEL, N

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PF270 IS ACUTE MYELOBLASTIC LEUKEMIA IN CHILDREN UNDER TWO YEARS OF AGE A SPECIFIC ENTITY? A REPORT FROM THE FRENCH ELAM02 STUDY GROUP von Blais, S., Boutroux, H., Pasquet, M., Leblanc, T., Fenneteau, O., Gandemer, V., Bertrand, Y., Ducassou, S., Michel, G., Nelken, B., Petit, A., Cuccuini, W., Gouache, E., Marceau, A., Baruchel, A., Lapillonne, H., Leverger, G.

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