Zobrazeno 1 - 7
of 7
pro vyhledávání: '"José María Raya"'
Autor:
Jesús M. Hernández, Blanca Xicoy, Joan Bargay, Elisa Luño, Benet Nomdedeu, Carme Pedro, Guillermo Sanz, Carmen Sanzo, José María Raya, Rosa Collado, Felix Carbonell, Miguel A. Gallart, Consuelo del Cañizo, Silvia Saumell, Leonor Arenillas, Francesc Solé, José Cervera, Luis Belloch, Lourdes Florensa, Teresa Vallespi
Publikováno v:
British Journal of Haematology. 159:311-321
Trisomy 8 is the most common chromosomal gain in myelodysplastic syndromes (MDS), however, little is known about the features of MDS with isolated trisomy 8 and the influence of additional cytogenetic aberrations. We determined the characteristics an
Autor:
Fernando Ramos, Guillermo Sanz, Beatriz Arrizabalaga, José María Raya, Esther Alonso, David Valcárcel, Alicia Bailen, María Díez-Campelo, Leonor Arenillas, Lourdes Florensa, Xavier Calvo, Mar Tormo, María Teresa Ardanaz, Elisa Luño, Carmen Pedro
Publikováno v:
Blood. 126:2866-2866
Introduction: Based on the 2008 World Health Organization classification (WHO 2008), erythroleukemia is defined by the presence of ≥50% erythroid precursors in bone marrow (BM) and ≥20% myeloblasts in the non-erythroid cell population. Multilinea
Autor:
Fernando Ramos, María Consuelo del Cañizo, Carmen Pedro, Esther Alonso, Beatriz Arrizabalaga, Lourdes Florensa, Alicia Bailen, Guillermo Sanz, Xavier Calvo, José María Raya, David Valcárcel, Mar Tormo, María Teresa Ardanaz, Elisa Luño, Leonor Arenillas
Publikováno v:
Blood. 126:2894-2894
Introduction: WHO classification of MDS is based on cytopenias, dysplasia, percentage of blasts in PB and BM, and cytogenetics. IPSS-R establishes BM blast subgroups (≤2%,2-10%) with independent impact in OS. Erythroid hyperplasia (≥50% of total
Autor:
Helena Pomares, Montserrat Arnan, Julia Montoro, Juan D. Rodríguez-Gambarte, Carmen Sanzo, Eduardo Ríos, Andres Jerez, Teresa Giménez, Elisa Luño, Carme Pedro, Raquel de Paz, Blanca Espinet, Judith Sánchez-Castro, Francesc Solé, Beatriz Arrizabalaga, Silvia Saumell, David Valcárcel, María Rodríguez-Rivera, José María Raya, Lourdes Florensa, Leonor Arenillas, Ana Maria Barral de Martinez
Publikováno v:
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
PLoS ONE
PLoS ONE, Vol 10, Iss 6, p e0129375 (2015)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS ONE
PLoS ONE, Vol 10, Iss 6, p e0129375 (2015)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
Isolated trisomy 8 is not considered presumptive evidence of myelodysplastic syndrome (MDS) in cases without minimal morphological criteria. One reason given is that trisomy 8 (+8) can be found as a constitutional mosaicism (cT8M). We tried to clarif
Autor:
María Consuelo del Cañizo, Albert Perez-Ladaga, Vera Adema, Joaquin Sanchez-Garcia, Carmen Sanzo, Mònica Bayés, Blanca Xicoy, Francesc Solé, Eduardo Rios, Rosario López, Rafael Bejar, Elisa Luño, Mar Mallo, Lurdes Zamora, Carmen Pedro, María Díez-Campelo, Leonor Arenillas, Paula Gomez-Marzo, Montserrat Arnan, Shawn Yost, Ivo Gut, Laura Palomo, Raquel de Paz, Angelina Lemes, Lourdes Florensa, José María Raya
Publikováno v:
Blood. 124:4635-4635
INTRODUCTION Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal myeloid stem cell disorders that are highly prevalent in elderly populations. MDS are characterized by inefficient hematopoiesis, peripheral blood (PB) cytopenias, and i
Autor:
Eduardo Rios, Laura Palomo, Rosario López, Vera Adema, Carmen Pedro, José María Raya, Shawn Yost, Consuelo del Cañizo, Albert Perez-Ladaga, Joaquín Sánchez, Angelina Lemes, Lourdes Florensa, Carmen Sanzo, Montserrat Arnan, Elisa Luño, Blanca Xicoy, Chun-Pei Cheng, Raquel de Paz, Leonor Arenillas, Mar Mallo, María Díez-Campelo, Francesc Solé, Lurdes Zamora, Olivier Harismendy, Rafael Bejar
Publikováno v:
Blood. 122:1551-1551
Introduction Myelodysplastic Syndromes (MDS) are a heterogeneous group of clonal myeloid stem cells disorders with high prevalence in the elderly characterized by inefficient hematopoiesis, peripheral blood (PB) cytopenias, and an increased risk of t
Autor:
Mario Cazzola, Esther Zipperer, Sylvie Hermouet, Susanne Schnittger, Lourdes Florensa, Julien Broséus, Marc Maynadié, Jyoti Nangalia, Morgane Mounier, Carlos Besses, Steven Richebourg, Torsten Haferlach, Eric Lippert, François Girodon, José María Raya, Norbert Gattermann, Claudia Haferlach, Erica Travaglino, Ulrich Germing, Luca Malcovati, Allou Kaoutar, Jaroslav Cermak, Richard Garand
Publikováno v:
Blood. 116:4113-4113
Abstract 4113 Introduction: Most of the data related to RARS-T, a rare disorder, involve small cohorts of patients. We aimed to analyze more patients also considering a variety of myelodysplastic or myeloproliferative disorders. Objective: To compare