Showing 1 - 5 results of 5 for search 'Lourdes Florensa', query time: 0.03s Refine Results
  1. 1
    TET2 gene is not deleted in chronic myelomonocytic leukemia: a FISH retrospective study

    TET2 gene is not deleted in chronic myelomonocytic leukemia: a FISH retrospective study by Mar Mallo, Gemma Osca, Julia Solórzano, Leonor Arenillas, Lourdes Florensa, Francesc Solé

    Published 2010-10-01
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  2. 2
    Reproducibility of the World Health Organization 2008 criteria for myelodysplastic syndromes

    Reproducibility of the World Health Organization 2008 criteria for myelodysplastic syndromes by Leonor Senent, Leonor Arenillas, Elisa Luño, Juan C. Ruiz, Guillermo Sanz, Lourdes Florensa

    Published 2013-04-01
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  3. 3
    Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis

    Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis by Susana Rives, Heike L. Pahl, Lourdes Florensa, Beatriz Bellosillo, Andrea Neusuess, Jesus Estella, Klaus-Michael Debatin, Elisabeth Kohne, Klaus Schwarz, Holger Cario

    Published 2007-05-01
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  4. 4
    Clinical features and course of refractory anemia with ring sideroblasts associated with marked thrombocytosis

    Clinical features and course of refractory anemia with ring sideroblasts associated with marked thrombocytosis by Julien Broseus, Lourdes Florensa, Esther Zipperer, Susanne Schnittger, Luca Malcovati, Steven Richebourg, Eric Lippert, Jaroslav Cermak, Jyoti Evans, Morgane Mounier, José Maria Raya, François Bailly, Norbert Gattermann, Torsten Haferlach, Richard Garand, Kaoutar Allou, Carlos Besses, Ulrich Germing, Claudia Haferlach, Erica Travaglino, Elisa Luno, Maria Angeles Pinan, Leonor Arenillas, Maria Rozman, Maria Luz Perez Sirvent, Bernardine Favre, Julien Guy, Esther Alonso, Nuhri Ahwij, Andrés Jerez, Sylvie Hermouet, Marc Maynadié, Mario Cazzola, François Girodon

    Published 2012-07-01
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  5. 5
    Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-

    Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q- by Mar Mallo, Leonor Arenillas, Blanca Espinet, Marta Salido, Jesús Mª Hernández, Eva Lumbreras, Mónica del Rey, Eva Arranz, Soraya Ramiro, Patricia Font, Olga González, Mónica Renedo, José Cervera, Esperanza Such, Guillermo F. Sanz, Elisa Luño, Carmen Sanzo, Miriam González, María José Calasanz, José Mayans, Carlos García-Ballesteros, Victoria Amigo, Rosa Collado, Isabel Oliver, Félix Carbonell, Encarna Bureo, Andrés Insunza, Lucrecia Yañez, María José Muruzabal, Elena Gómez-Beltrán, Rafael Andreu, Pilar León, Valle Gómez, Ángeles Sanz, Natalia Casasola, Esperanza Moreno, Adrián Alegre, María Luisa Martín, Carmen Pedro, Sergi Serrano, Lourdes Florensa, Francesc Solé

    Published 2008-07-01
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