Výsledky vyhledávání - "Carole Conejero"

Akademický článek

Positive impact of molecular analysis on prognostic scores in essential thrombocythemia: a single center prospective cohort experience

Autor: Damien Luque Paz, Olivier Mansier, Jérémie Riou, Carole Conejero, Lydia Roy, Célia Belkhodja, Valérie Ugo, Stéphane Giraudier

Publikováno v: Haematologica, Vol 104, Iss 4 (2019)

Externí odkaz: https://doaj.org/article/7f8126029435413b8090e08908ddf6f7

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Emergence of MPLW515 mutation in a patient with CALR deletion: Evidence of secondary acquisition of MPL mutation in the CALR clone

Autor: Catherine Cordonnier, Julien Moroch, Quentin Barathon, Stéphane Giraudier, Nicolas Partouche, Michel Tulliez, Carole Conejero

Publikováno v: Hematological Oncology. 36:336-339

Myeloproliferative neoplasms are characterized by transduction pathway recognized as mutually exclusive molecular abnormalities such as BCR-ABL translocation, JAK2V617F or JAK2 exon 12 mutations, MPL w515, and CALR mutations. However, in some rare ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c0aec34debc78e31e981c99aa1fc1569
https://doi.org/10.1002/hon.2431

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Positive impact of molecular analysis on prognostic scores in essential thrombocythemia: a single center prospective cohort experience

Autor: Jérémie Riou, Stéphane Giraudier, Damien Luque Paz, Célia Belkhodja, Olivier Mansier, Valérie Ugo, Lydia Roy, Carole Conejero

Publikováno v: Haematologica
Haematologica, 2019, 104 (4), pp.e134-e137. ⟨10.3324/haematol.2018.197699⟩
Haematologica, Ferrata Storti Foundation, 2019, 104 (4), pp.e134-e137. ⟨10.3324/haematol.2018.197699⟩

DLP, OM and JR contributed equally to this work.; International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecd56c342d5b25947f65492e1f9275b3
https://www.hal.inserm.fr/inserm-02516720/document

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Clinical and biological characterization of MPN patients harboring two driver mutations, a French intergroup of myeloproliferative neoplasms (FIM) study

Autor: Jean-François Viallard, Jasmine Chauzeix, Didier Adiko, Valérie Ugo, Jean-Christophe Ianotto, Olivier Fitoussi, Mohamed Touati, Stéphane Giraudier, Olivier Mansier, Françoise Boyer, Yannick Le Bris, Damien Luque Paz, Jérémie Riou, Eric Lippert, Marie C. Béné, Aurélie Chauveau, Carole Conejero

Publikováno v: American Journal of Hematology
American Journal of Hematology, 2018, 93 (4), pp.E84-E86. ⟨10.1002/ajh.25014⟩
American Journal of Hematology, Wiley, 2018, 93 (4), pp.E84-E86. ⟨10.1002/ajh.25014⟩
American Journal of Hematology, Wiley, 2018, 93 (4), pp.E84-E86. 〈10.1002/ajh.25014〉

International audience; no abstract

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07c1b941872e09bf75b017687c0bfb94
https://www.hal.inserm.fr/inserm-01813777

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Unexplained thrombocytosis: association of Baltimore polymorphism with germline MPL nonsense mutation

Autor: Gil Letort, Stéphane Giraudier, Emmanuelle Verger, Bruno Cassinat, Carole Conejero, Christine Chomienne

Publikováno v: British Journal of Haematology. 175:167-169

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::799efd4688ffdcc71fd630e5a612af98
https://doi.org/10.1111/bjh.13840

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Essential thrombocythemias without V617F JAK2 mutation are clonal hematopoietic stem cell disorders

Autor: J J Kiladjian, Jean Briere, Bernard Grandchamp, Stéphane Giraudier, Nicole Balitrand, Carole Conejero, N. Elkassar, Pierre Fenaux, Gilles Hetet, Bruno Cassinat, Christine Chomienne

Publikováno v: Leukemia. 20(6)

Essential thrombocythemias without V617F JAK2 mutation are clonal hematopoietic stem cell disorders

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b8bedba9d5e207c66cf8d39973239c6
https://pubmed.ncbi.nlm.nih.gov/16598303

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GATA 1: pArg202Thr, a New GATA 1 Mutation Involved in a Severe Dyserythropoietic Phenotype

Autor: Chadia Mekki, Lydie Da Costa, Stephane Giraudier, Valentine Brousse, Serge Pissard, Mariane de Montalembert, Carole Conejero, Serge Hovhannisyan

Publikováno v: Blood. 124:1343-1343

Intro: Dyserythropoiesis is a growing class of inherited diseases of various severities in which genes encoding for proteins involved in cellular trafficking, chromatin dynamic or transacting factors restricted to red cells maturation, are mutated. B

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d7258c2dd8e1000c945ac69da516204
https://doi.org/10.1182/blood.v124.21.1343.1343

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Akademický článek

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Analysis of JAK2 Mutation in Essential Thrombocythemia (ET) Patients with Monoclonal and Polyclonal X-Chromosome Inactivation Patterns (XCIPs)

Autor: Carole Conejero, Gilles Hetet, Stéphane Giraudier, Jean-Jacques Kiladjian, Pierre Fenaux, Nicole Balitrand, Bruno Cassinat, N. Elkassar, Claude Gardin, Christine Chomienne, Bernard Grandchamp

Publikováno v: Blood. 106:2603-2603

Background: ET is considered as a hematopoietic stem cell disorder, closely related to polycythemia vera (PV). Several studies in female ET patients, using XCIPs analysis, have shown the persistence of polyclonal patterns in a subset of patients, the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a5922af1018d1fe6fd97257e92af7d4e
https://doi.org/10.1182/blood.v106.11.2603.2603

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