Resultats de la cerca - François Girodon
- Mostrar 1 - 20 resultats de 27
- Anar a la pàgina següent
-
1
-
2
-
3
-
4
Latent myeloproliferative disorder revealed by the JAK2-V617F mutation and endogenous megakaryocytic colonies in patients with splanchnic vein thrombosis per Marjorie Boissinot, Éric Lippert, François Girodon, Irène Dobo, Marc Fouassier, Claude Masliah, Vincent Praloran, Sylvie Hermouet
Publicat 2006Carta -
5
The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera per Éric Lippert, Marjorie Boissinot, Róbert Královics, François Girodon, Irène Dobo, Vincent Praloran, Nathalie Boiret‐Dupré, Radek C. Skoda, Sylvie Hermouet
Publicat 2006Artigo -
6
Usefulness of the eosin‐5′‐maleimide cytometric method as a first‐line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein elect... per François Girodon, Loïc Garçon, Emilie Bergoin, Marie Largier, J. Delaunay, Madeleine Fénéant‐Thibault, Marc Maynadié, Gérard Couillaud, Sophie Moreira, Thérèse Cynober
Publicat 2007Carta -
7
Leukemic blasts in transformed JAK2-V617F–positive myeloproliferative disorders are frequently negative for the JAK2-V617F mutation. per Alexandre Theocharides, Marjorie Boissinot, François Girodon, Richard Garand, Soon-Siong Teo, Éric Lippert, Pascaline Talmant, André Tichelli, Sylvie Hermouet, Radek C. Skoda
Publicat 2007Artigo -
8
Clonal analysis of deletions on chromosome 20q and JAK2-V617F in MPD suggests that del20q acts independently and is not one of the predisposing mutations for JAK2-V617F per Franz X. Schaub, Roland Jäger, Renate Looser, Hui Hao-Shen, Sylvie Hermouet, François Girodon, André Tichelli, Heinz Gisslinger, Róbert Královics, Radek C. Skoda
Publicat 2008Artigo -
9
Twenty-five years of epidemiological recording on myeloid malignancies: data from the specialized registry of hematologic malignancies of Cote d'Or (Burgundy, France) per Marc Maynadié, François Girodon, I. Manivet-Janoray, Morgane Mounier, Francine Mugneret, François Bailly, Bernardine Favre, D Caillot, Tony Petrella, M. Flesch, Paule‐Marie Carli
Publicat 2010Artigo -
10
Low rate of calreticulin mutations in refractory anaemia with ring sideroblasts and marked thrombocytosis per Julien Broséus, Éric Lippert, Ashot S. Harutyunyan, Sabine Jeromin, E. Zipperer, Lourdes Florensa, Jelena D. Milosevic Feenstra, Torsten Haferlach, Ulrich Germing, Elisa Luño, Susanne Schnittger, Róbert Královics, François Girodon
Publicat 2014Carta -
11
Paroxysmal nocturnal hemoglobinuria and pregnancy before the eculizumab era: the French experience per Sophie de Guibert, Régis Peffault de Latour, Nathalie Varoqueaux, Hélène Labussière, Bernard Rio, Dominique Jaulmes, Jean‐Richard Eveillard, Stéphanie Dulucq, Anne Marie Stoppa, Didier Bouscary, François Girodon, Bernard Bonnotte, D. Laskri, Gèrard Socié, Thierry Lamy
Publicat 2011Artigo -
12
Monoclonal IgG in MGUS and multiple myeloma targets infectious pathogens per Adrien Bosseboeuf, Delphine Féron, Anne Tallet, Cédric Rossi, Cathy Charlier, Laurent Garderet, Denis Caillot, Philippe Moreau, Marina Cardó‐Vila, Renata Pasqualini, Wadih Arap, Alfreda D. Nelson, Bridget S. Wilson, Hélène Perreault, Éric Piver, Pierre Weigel, François Girodon, Jean Harb, Edith Bigot‐Corbel, Sylvie Hermouet
Publicat 2017Artigo -
13
Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?) per Celeste Bento, Helena Almeida, Tabita Maia, Luís Relvas, Ana Catarina Oliveira, Cédric Rossi, François Girodon, Carlos Fernández-Lago, Ascension Aguado‐Diaz, Cristina Fraga, Ricardo Marques da Costa, Ana Luiza Rosa de Araújo, João S. Silva, Helena Vitória, Natalina Miguel, Maria Pedro Silveira, Guillermo Martín–Núñez, Letícia Ribeiro
Publicat 2013Artigo -
14
Concordance of assays designed for the quantification of JAK2V617F: a multicenter study per Éric Lippert, François Girodon, E. Hammond, Jaroslav Jelı́nek, N. Scott Reading, Boris Fehse, Katy Hanlon, M. H. A. Hermans, C. Richard, Sabina Świerczek, Valérie Ugo, Serge Carillo, Véronique Harrivel, Christophe Marzac, Daniela Pietra, Marta Sobas, Morgane Mounier, Marina Migeon, Sian Ellard, Nicolaus Kröger, Richard Herrmann, Josef T. Prchal, Radek C. Skoda, Sylvie Hermouet
Publicat 2008Artigo -
15
Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution per Xénia Cabagnols, Jean‐Philippe Defour, Valérie Ugo, Jean‐Christophe Ianotto, Pascal Mossuz, Julie Mondet, François Girodon, Jean Alexandre, Olivier Mansier, Jean‐François Viallard, Éric Lippert, Anne Murati, Julien Mozziconacci, Pascale Saussoy, Marie-Christine Vekemans, L. Knoops, Florence Pasquier, Vincent Ribrag, Éric Solary, Isabelle Plo, Stefan N. Constantinescu, Nicole Casadevall, William Vainchenker, Christophe Marzac, Olivier Bluteau
Publicat 2014Carta -
16
Cohen syndrome is associated with major glycosylation defects per Laurence Duplomb, Sandrine Duvet, Damien Picot, Gaëtan Jégo, Salima El Chehadeh-Djebbar, Nathalie Marle, Nadège Gigot, Bernard Aral, Virginie Carmignac, Julien Thévenon, Estelle Lopez, Jean‐Baptiste Rivière, André Klein, Christophe Philippe, Nathalie Droin, Edward Blair, François Girodon, Jean Donadieu, Christine Bellanné‐Chantelot, Laurent Delva, Jean‐Claude Michalski, Éric Solary, Laurence Faivre, François Foulquier, Christel Thauvin‐Robinet
Publicat 2013Artigo -
17
Inferring the dynamics of mutated hematopoietic stem and progenitor cells induced by IFNα in myeloproliferative neoplasms per Matthieu Mosca, Gurvan Hermange, Amandine Tisserand, Robert Noble, Christophe Marzac, Caroline Marty, Cécile Le Sueur, Hugo Campario, Gaëlle Vertenoeil, Mira El-Khoury, Cyril Catelain, Philippe Rameau, Cyril Gella, Julien Lenglet, Nicole Casadevall, Rémi Favier, Éric Solary, Bruno Cassinat, Jean‐Jacques Kiladjian, Stefan N. Constantinescu, Florence Pasquier, Michael Hochberg, Hana Raslová, Jean‐Luc Villeval, François Girodon, William Vainchenker, Paul-Henry Cournède, Isabelle Plo
Publicat 2021Artigo -
18
A prognostic model to predict survival in 867 World Health Organization–defined essential thrombocythemia at diagnosis: a study by the International Working Group on Myelofibrosis... per Francesco Passamonti, Jürgen Thiele, François Girodon, Elisa Rumi, Alessandra Carobbio, Heinz Gisslinger, Hans Michael Kvasnicka, Marco Ruggeri, Maria Luigia Randi, Naseema Gangat, Alessandro M. Vannucchi, Andrea Gianatti, Bettina Gisslinger, Leonhard Müllauer, Francesco Rodeghiero, Emanuele S. G. d'Amore, Irene Bertozzi, Curtis A. Hanson, Emanuela Boveri, Filippo Marino, Margherita Maffioli, Domenica Caramazza, Elisabetta Antonioli, Valentina Carrai, Veronika Buxhofer‐Ausch, Cristiana Pascutto, Mario Cazzola, Tiziano Barbui, Ayalew Tefferi
Publicat 2012Artigo -
19
Clinical features and course of refractory anemia with ring sideroblasts associated with marked thrombocytosis per Julien Broséus, Lourdes Florensa, E. Zipperer, Susanne Schnittger, Luca Malcovati, Steven Richebourg, Éric Lippert, Jaroslav Čermák, J. D. Evans, Morgane Mounier, José María Raya, François Bailly, Norbert Gattermann, Torsten Haferlach, Richard Garand, Kaoutar Allou, Carlos Besses, Ulrich Germing, Claudia Haferlach, Erica Travaglino, Elisa Luño, M.A. Piñán, Leonor Arenillas, Marı́a Rozman, M. L. Perez Sirvent, Bernardine Favre, Julien Guy, Esther Alonso, Nuri Ahwij, A. Jerez, Sylvie Hermouet, Marc Maynadié, M. Cazzola, François Girodon
Publicat 2012Artigo -
20
Splanchnic vein thromboses associated with myeloproliferative neoplasms: An international, retrospective study on 518 cases per Emanuela Sant’Antonio, Paola Guglielmelli, Lisa Pieri, Massimo Primignani, Maria Luigia Randi, Claudia Santarossa, Elisa Rumi, Francisco Cervantes, Federica Delaini, Alessandra Carobbio, Silvia Betti, Elena Rossi, Noa Lavi, Claire Harrison, Natalia Curto‐García, Heinz Gisslinger, Bettina Gisslinger, Giorgina Specchia, Alessandra Ricco, Nicola Vianelli, Nicola Polverelli, Maya Koren‐Michowitz, Marco Ruggeri, François Girodon, Martin Ellis, Alessandra Iurlo, Francesco Mannelli, Lara Mannelli, Benedetta Sordi, Giuseppe Gaetano Loscocco, Mario Cazzola, Valerio De Stefano, Tiziano Barbui, Ayalew Tefferi, Alessandro M. Vannucchi
Publicat 2019Artigo
Eines de cerca:
Matèries relacionades
Medicine
Biology
Genetics
Internal medicine
Gene
Immunology
Bone marrow
Mutation
Essential thrombocythemia
Myelofibrosis
Polycythemia vera
Gastroenterology
Cancer research
Myeloproliferative Disorders
JAK2 V617F
Molecular biology
Surgery
Thrombosis
Endoplasmic reticulum
Hematology
Leukemia
Myeloid leukemia
Pathology
Pediatrics
Physics
Biochemistry
Calreticulin
Cohort
Haematopoiesis
Incidence (geometry)