Search Results - "Perot, Christine"

Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study by Balgobind, Brian V., Raimondi, Susana C., Harbott, Jochen, Zimmermann, Martin, Alonzo, Todd A., Auvrignon, Anne, Beverloo, H. Berna, Chang, Myron, Creutzig, Ursula, Dworzak, Michael N., Forestier, Erik, Gibson, Brenda, Hasle, Henrik, Harrison, Christine J., Heerema, Nyla A., Kaspers, Gertjan J.L., Leszl, Anna, Litvinko, Nathalia, Nigro, Luca Lo, Morimoto, Akira, Perot, Christine, Pieters, Rob, Reinhardt, Dirk, Rubnitz, Jeffrey E., Smith, Franklin O., Stary, Jan, Stasevich, Irina, Strehl, Sabine, Taga, Takashi, Tomizawa, Daisuke, Webb, David, Zemanova, Zuzana, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M.

“…Translocations involving chromosome 11q23 frequently occur in pediatric acute myeloid leukemia (AML) and are associated with poor prognosis. In most cases, the…”
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Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome by 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

“…Patients with the Shwachman-Diamond syndrome often develop hematologic complications. No risk factors for these complications have so far been identified. The…”
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High resolution genome-wide analysis of chromosomal alterations in Burkitt's lymphoma by Toujani, Saloua, Dessen, Philippe, Ithzar, Nathalie, Danglot, Gisèle, Richon, Catherine, Vassetzky, Yegor, Robert, Thomas, Lazar, Vladimir, Bosq, Jacques, Da Costa, Lydie, Pérot, Christine, Ribrag, Vincent, Patte, Catherine, Wiels, Jöelle, Bernheim, Alain

“…Additional chromosomal abnormalities are currently detected in Burkitt's lymphoma. They play major roles in the progression of BL and in prognosis. The genes…”
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Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogénétique Hématologique study by Coyaud, Etienne, Struski, Stephanie, Prade, Nais, Familiades, Julien, Eichner, Ruth, Quelen, Cathy, Bousquet, Marina, Mugneret, Francine, Talmant, Pascaline, Pages, Marie-Pierre, Lefebvre, Christine, Penther, Dominique, Lippert, Eric, Nadal, Nathalie, Taviaux, Sylvie, Poppe, Bruce, Luquet, Isabelle, Baranger, Laurence, Eclache, Virginie, Radford, Isabelle, Barin, Carole, Mozziconacci, Marie-Joëlle, Lafage-Pochitaloff, Marina, Antoine-Poirel, Hélène, Charrin, Christiane, Perot, Christine, Terre, Christine, Brousset, Pierre, Dastugue, Nicole, Broccardo, Cyril

“…PAX5 is the main target of somatic mutations in acute B lymphoblastic leukemia (B-ALL). We analyzed 153 adult and child B-ALL harboring karyotypic…”
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Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study by Coenen, Eva A., Raimondi, Susana C., Harbott, Jochen, Zimmermann, Martin, Alonzo, Todd A., Auvrignon, Anne, Beverloo, H. Berna, Chang, Myron, Creutzig, Ursula, Dworzak, Michael N., Forestier, Erik, Gibson, Brenda, Hasle, Henrik, Harrison, Christine J., Heerema, Nyla A., Kaspers, Gertjan J.L., Leszl, Anna, Litvinko, Nathalia, Lo Nigro, Luca, Morimoto, Akira, Perot, Christine, Reinhardt, Dirk, Rubnitz, Jeffrey E., Smith, Franklin O., Stary, Jan, Stasevich, Irina, Strehl, Sabine, Taga, Takashi, Tomizawa, Daisuke, Webb, David, Zemanova, Zuzana, Pieters, Rob, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M.

“…We previously demonstrated that outcome of pediatric 11q23/MLL-rearranged AML depends on the translocation partner (TP). In this multicenter international…”
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Neurofibromatosis‐1 gene deletions and mutations in de novo adult acute myeloid leukemia by Boudry‐Labis, Elise, Roche‐Lestienne, Catherine, Nibourel, Olivier, Boissel, Nicolas, Terre, Christine, Perot, Christine, Eclache, Virginie, Gachard, Nathalie, Tigaud, Isabelle, Plessis, Ghislaine, Cuccuini, Wendy, Geffroy, Sandrine, Villenet, Céline, Figeac, Martin, Leprêtre, Frederic, Renneville, Aline, Cheok, Meyling, Soulier, Jean, Dombret, Hervé, Preudhomme, Claude

“…Germline heterozygous alterations of the tumor‐suppressor gene neurofibromatosis‐1 (NF1) lead to neurofibromatosis type 1, a genetic disorder characterized by…”
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High WT1 Expression After Induction Therapy Predicts High Risk of Relapse and Death in Pediatric Acute Myeloid Leukemia by LAPILLONNE, Hélène, RENNEVILLE, Aline, DEHEE, Axelle, BELLMAN, Francoise, ADAM, Mircéa, LABOPIN, Myriam, DOUAY, Luc, LEVERGER, Guy, PREUDHOMME, Claude, LANDMAN-PARKER, Judith, AUVRIGNON, Anne, FLAMANT, Cyril, BLAISE, Annick, PEROT, Christine, LAI, Jean-Luc, BALLERINI, Paola, MAZINGUE, Francoise, FASOLA, Sylvie

“…To determine whether minimal residual disease (MRD) measured by Wilms' tumor gene 1 (WT1) expression is a prognostic marker in pediatric acute myeloid leukemia…”
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Unimpaired terminal erythroid differentiation and preserved enucleation capacity in myelodysplastic 5q(del) clones: a single cell study by GARDERET, Laurent, KOBARI, Ladan, MAZURIER, Christelle, DE WITTE, Caroline, GIARRATANA, Marie-Catherine, PEROT, Christine, CLAUDE GORIN, Norbert, LAPILLONNE, Hélène, DOUAY, Luc

“…Anemia is a characteristic of myelodysplastic syndromes, such as the rare 5q- syndrome, but its mechanism remains unclear. In particular, data are lacking on…”
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Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH) by Dastugue, Nicole, Lafage-Pochitaloff, Marina, Pagès, Marie-Pierre, Radford, Isabelle, Bastard, Christian, Talmant, Pascaline, Mozziconacci, Marie Joelle, Léonard, Claude, Bilhou-Nabéra, Christelle, Cabrol, Christine, Capodano, Anne-Marie, Cornillet-Lefebvre, Pascale, Lessard, Michel, Mugneret, Francine, Pérot, Christine, Taviaux, Sylvie, Fenneteaux, Odile, Duchayne, Eliane, Berger, Roland

“…To draw the cytogenetic profile of childhood and adult acute megakaryoblastic leukemia (M7), the Groupe Français de Cytogénétique Hématologique collected 53…”
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t(6;9)(p22;q34)/DEK-NUP214-rearranged pediatric myeloid leukemia: an international study of 62 patients by Sandahl, Julie Damgaard, Coenen, Eva A, Forestier, Erik, Harbott, Jochen, Johansson, Bertil, Kerndrup, Gitte, Adachi, Souichi, Auvrignon, Anne, Beverloo, H Berna, Cayuela, Jean-Michel, Chilton, Lucy, Fornerod, Maarten, de Haas, Valérie, Harrison, Christine J, Inaba, Hiroto, Kaspers, Gertjan J L, Liang, Der-Cherng, Locatelli, Franco, Masetti, Riccardo, Perot, Christine, Raimondi, Susana C, Reinhardt, Katarina, Tomizawa, Daisuke, von Neuhoff, Nils, Zecca, Marco, Zwaan, C Michel, van den Heuvel-Eibrink, Marry M, Hasle, Henrik

“…Acute myeloid leukemia with t(6;9)(p22;q34) is listed as a distinct entity in the 2008 World Health Organization classification, but little is known about the…”
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SPRED1 disorder and predisposition to leukemia in children by Pasmant, Eric, Ballerini, Paola, Lapillonne, Helene, Perot, Christine, Vidaud, Dominique, Leverger, Guy, Landman-Parker, Judith

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Cytogenetics in the management of children and adult acute lymphoblastic leukemia (ALL): an update by the Groupe francophone de cytogénétique hématologique (GFCH) by Baranger, Laurence, Cuccuini, Wendy, Lefebvre, Christine, Luquet, Isabelle, Perot, Christine, Radford, Isabelle, Lafage-Pochitaloff, Marina

“…Cytogenetic analyses (karyotype and, if necessary, appropriate complementary FISH analyses) are mandatory at diagnosis in acute lymphoblastic leukemia (ALL) as…”
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Interest of the Association Azacitidine-Lenalidomide As Front Line Therapy in High-Risk Myelodysplasia (MDS) or Acute Myeloid Leukemia (AML) with Complex Karyotype by Scherman, Elodie, Malak, Sandra, Perot, Christine, Gorin, Norbert C., Rubio, Marie T, Isnard, Françoise

“…Abstract 5035 Results of intensive chemotherapy (ICT) in myelodysplasia (MDS) or secondary acute myeloid leukaemia (sAML) are poor, particularly in the…”
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Interest of cytogenetic and FISH evaluation for prognosis evaluation in 198 patients with acute myeloid leukemia in first complete remission in a single institution by Hirsch, Pierre, Labopin, Myriam, Viguié, Frank, Perot, Christine, Isnard, Françoise, Mamez, Anne-Claire, Bilhou-Nabera, Chrystèle, Marzac, Christophe, Delhommeau, François, Lapusan, Simona, Marie, Jean Pierre, Mohty, Mohamad, Legrand, Ollivier

“…Highlights • Cytogenetic complete remission is not associated with prognosis in 198 AML patients. • FISH remission is associated with prognosis in 52 AML…”
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HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis by Ballerini, Paola, Blaise, Annick, Busson-Le Coniat, Maryvonne, Su, Xin Ying, Zucman-Rossi, Jessica, Adam, Mircea, van den Akker, Jacqueline, Perot, Christine, Pellegrino, Beatrice, Landman-Parker, Judith, Douay, Luc, Berger, Roland, Bernard, Olivier A.

“…The most frequent oncogenic activation events characterized in childhood T acute lymphoblastic leukemia (T-ALL) result in the transcriptional activation of…”
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Translocation t(6;9)(p22;q34)/DEK-NUP214 rearranged Pediatric AML: A Retrospective International Study by Sandahl, Julie Damgaard, Coenen, Eva A., Forestier, Erik, Harbott, Jochen, Johansson, Bertil, Kerndrup, Gitte, Adachi, Souichi, Auvrignon, Anne, Beverloo, H. Berna, Chilton, Lucy, de Haas, Valerie, Harrison, Christine J, Inaba, Hiroto, Kaspers, Gertjan J.L., Liang, Der-Cherng, Lin, Kuo-Sin, Masetti, Riccardo, Perot, Christine, Pession, Andrea, Raimondi, Susana C., Reinhardt, Katarina, Tomizawa, Daisuke, von Neuhoff, Nils, Zecca, Marco, van den Heuvel-Eibrink, Marry M., Hasle, Henrik

“…Abstract 538 The cytogenetic subgroup t(6;9)(p22;q34), previously often reported as a breakpoint in 6p23, is defined as a distinct entity in the 2008 WHO…”
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A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL) by Charrin, Christiane, Thomas, Xavier, Ffrench, Martine, Le, Quoc-Hung, Andrieux, Joris, Mozziconacci, Marie-Joelle, Laï, Jean-Luc, Bilhou-Nabera, Chrystele, Michaux, Lucienne, Bernheim, Alain, Bastard, Christian, Mossafa, Hossein, Perot, Christine, Maarek, Odile, Boucheix, Claude, Lheritier, Véronique, Delannoy, André, Fière, Denis, Dastugue, Nicole

“…To reveal the relationship between hypodiploidy with 30 to 39 chromosomes and near-triploidy in acute lymphoblastic leukemia (ALL), we studied 24 patients…”
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Deletion of the Tumor Suppressor Gene NF1 Is Found In 3.5% of 485 De Novo Adult Myeloid Leukemia and Is Correlated with Unfavourable Cytogenetic: On Behalf of the ALFA Group by Labis, Elise, Roche-Lestienne, Catherine, Nibourel, Olivier, Boissel, Nicolas, Roumier, Christophe, Terre, Christine, Perot, Christine, Eclache, Virginie, Gachard, Nathalie, Tigaud, Isabelle, Plessis, Ghislaine, Cuccuini, Wendy, Geffroy, Sandrine, Helevaut, Nathalie, Quief, Sabine, Figeac, Martin, Renneville, Aline, Cheok, Meyling, Quesnel, Bruno, Dombret, Herve, Preudhomme, Claude

“…Abstract 4171 NF1 acts as a tumor-suppressor gene by encoding neurofibromin1, a GTPase-activating protein (GAP) inhibiting Ras signaling pathway. Germline…”
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Clinical Impact of Additional Cytogenetic Aberrations and Complex Karyotype In Pediatric 11q23/MLL-Rearranged AML: Results from an International Retrospective Study by Coenen, Eva A, Raimondi, Susana C., Harbott, Jochen, Martin, Zimmermann, Balgobind, Brian V, Alonzo, Todd A., Auvrignon, Anne, Beverloo, Berna, Chang, Myron, Creutzig, Ursula, Dworzak, Michael, Forestier, Erik, Gibson, Brenda, Hasle, Henrik, Harrison, Christine J, Heerema, Nyla A., Kaspers, Gertjan J., Leszl, Anna, Litvinko, Nathalia, Nigro, Luca lo, Morimoto, Akira, Perot, Christine, Reinhardt, Dirk, Rubnitz, Jeffrey, Smith, Franklin O., Stary, Jan, Stasevich, Irina, Strehl, Sabine, Taga, Takashi, Tomizawa, Daisuke, Webb, David, Zemanova, Zuzana, Pieters, Rob, Zwaan, C. Michel, Heuvel-Eibrink, Marry van den

“…Abstract 762 Pediatric AML is a heterogeneous disease. We showed that differential outcomes of 11q23/MLL-rearranged AML depend on the fusion partner involved…”
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Prognostic Significance of SALL4 Expression Levels in Paediatric Acute Myeloid Leukaemia (AML) by Ballerini, Paola, Boelle, Pierre-Yves, Deswarte, Caroline, Auvrignon, Anne, Couchy, Gabrielle, Parker, Judith Landman, Robert, Alain, Nelken, Brigitte, Adam, Mircea, Lapillonne, Helene, Delabesse, Eric, Perot, Christine, Lai, Jean Luc, Dastugue, Nicole, Preudhomme, Claude, Zucman-Rossi, Jessica, Leverger, Guy

“…Pediatric AML still represent an unfavourable disease resulting from the heterogeneous clonal expansion of malignant transformed haematopoietic stem or…”
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