Platelet Counting: Ugly Traps and Good Advice. Proposals from the French-Speaking Cellular Hematology Group (GFHC)

por Baccini, Véronique, Geneviève, Franck, Jacqmin, Hugues, Chatelain, Bernard, Girard, Sandrine, Wuilleme, Soraya, Vedrenne, Aurélie, Guiheneuf, Eric, Toussaint-Hacquard, Marie, Everaere, Fanny, Soulard, Michel, Lesesve, Jean-François, Bardet, Valérie
Publicado 2020

Platelet caspase‐1 and Bruton tyrosine kinase activation in patients with COVID‐19 is associated with disease severity and reversed in vitro by ibrutinib

por Claude, Livia, Martino, Frédéric, Hermand, Patricia, Chahim, Bassel, Roger, Pierre‐Marie, de Bourayne, Marie, Garnier, Yohann, Tressieres, Benoit, Colin, Yves, Le Van Kim, Caroline, Romana, Marc, Baccini, Véronique
Publicado 2022

Acquired TET2 mutation in one patient with familial platelet disorder with predisposition to AML led to the development of pre‐leukaemic clone resulting in T2‐ALL and AML‐M0

por Manchev, Vladimir T., Bouzid, Hind, Antony‐Debré, Iléana, Leite, Betty, Meurice, Guillaume, Droin, Nathalie, Prebet, Thomas, Costello, Régis T., Vainchenker, William, Plo, Isabelle, Diop, M'boyba, Macintyre, Elizabeth, Asnafi, Vahid, Favier, Rémi, Baccini, Véronique, Raslova, Hana
Publicado 2016

Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders

por Latger-Cannard, Veronique, Philippe, Christophe, Bouquet, Alexandre, Baccini, Veronique, Alessi, Marie-Christine, Ankri, Annick, Bauters, Anne, Bayart, Sophie, Cornillet-Lefebvre, Pascale, Daliphard, Sylvie, Mozziconacci, Marie-Joelle, Renneville, Aline, Ballerini, Paola, Leverger, Guy, Sobol, Hagay, Jonveaux, Philippe, Preudhomme, Claude, Nurden, Paquita, Lecompte, Thomas, Favier, Remi
Publicado 2016

Perls’ Stain Guidelines from the French-Speaking Cellular Hematology Group (GFHC)

por Lours, Camille, Cottin, Laurane, Wiber, Margaux, Andrieu, Valérie, Baccini, Véronique, Baseggio, Lucile, Brouzes, Chantal, Chatelain, Bernard, Daliphard, Sylvie, Fenneteau, Odile, Geneviève, Franck, Girard, Sandrine, Leymarie, Vincent, Maloum, Karim, Rieu, Jean-Baptiste, Sebahoun, Gérard, Sudaka, Isabelle, Troussard, Xavier, Wagner-Ballon, Orianne, Wuilleme, Soraya, Bardet, Valérie, Lesesve, Jean-François
Publicado 2022

Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features

por Saultier, Paul, Vidal, Léa, Canault, Matthias, Bernot, Denis, Falaise, Céline, Pouymayou, Catherine, Bordet, Jean-Claude, Saut, Noémie, Rostan, Agathe, Baccini, Véronique, Peiretti, Franck, Favier, Marie, Lucca, Pauline, Deleuze, Jean-François, Olaso, Robert, Boland, Anne, Morange, Pierre Emmanuel, Gachet, Christian, Malergue, Fabrice, Fauré, Sixtine, Eckly, Anita, Trégouët, David-Alexandre, Poggi, Marjorie, Alessi, Marie-Christine
Publicado 2017

The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11

por Lafage-Pochitaloff, Marina, Gerby, Bastien, Baccini, Véronique, Largeaud, Laetitia, Fregona, Vincent, Prade, Naïs, Juvin, Pierre-Yves, Jamrog, Laura, Bories, Pierre, Hébrard, Sylvie, Lagarde, Stéphanie, Mansat-De Mas, Véronique, Dovey, Oliver M., Yusa, Kosuke, Vassiliou, George S., Jansen, Joop H., Tekath, Tobias, Rombaut, David, Ameye, Geneviève, Barin, Carole, Bidet, Audrey, Boudjarane, John, Collonge-Rame, Marie-Agnès, Gervais, Carine, Ittel, Antoine, Lefebvre, Christine, Luquet, Isabelle, Michaux, Lucienne, Nadal, Nathalie, Poirel, Hélène A., Radford-Weiss, Isabelle, Ribourtout, Bénédicte, Richebourg, Steven, Struski, Stéphanie, Terré, Christine, Tigaud, Isabelle, Penther, Dominique, Eclache, Virginie, Fontenay, Michaela, Broccardo, Cyril, Delabesse,, Eric
Publicado 2022