Search Results - "Ivars, David"

Fluorescence in situ hybridization analysis does not increase detection rate for trisomy 8 in chronic myelomonocytic leukemia by Saumell, Sílvia, Florensa, Lourdes, Rodríguez-Rivera, María, Pedro, Carme, Hernández-Rivas, Jesús María, Lumbreras, Eva, Abáigar, María, Collado, Rosa, Ivars, David, Carbonell, Félix, Marugán, Isabel, Tormo, Mar, Botia, Mercedes, Piñan, María Ángeles, Ancín, Idoia, González, Teresa, Varela, Nicolás Díaz, Grau, Javier, Granada, Isabel, Ruiz, Neus, Martín, María Luisa, Fernández-Guijarro, Manuela, Duarte, José-Joaquín, Calasanz, María José, Larrayoz, María José, Solé, Francesc

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Oxidative imbalance in low/intermediate-1-risk myelodysplastic syndrome patients: The influence of iron overload by Ivars, David, Orero, María Teresa, Javier, Karla, Díaz-Vico, Laura, García-Giménez, José Luis, Mena, Salvador, Tormos, Carmen, Egea, Mercedes, Pérez, Pedro Luis, Arrizabalaga, Beatriz, Ruiz, María Ángeles, Yagüe, Nuria, Tormo, Mar, Sancho-Tello, Reyes, Gomes, Angela, Algueró, Carmen, O'Connor, José Enrique, Sáez, Guillermo T., Carbonell, Félix, Collado, Rosa

“…To assess the generation of reactive oxygen species (ROS) and the involvement of the main antioxidant pathways in low/intermediate-1-risk myelodysplastic…”
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Early ROS-mediated DNA damage and oxidative stress biomarkers in Monoclonal B Lymphocytosis by Collado, Rosa, Oliver, Isabel, Tormos, Carmen, Egea, Mercedes, Miguel, Amparo, Cerdá, Concha, Ivars, David, Borrego, Silvia, Carbonell, Felix, Sáez, Guillermo T

“…Abstract Monoclonal B Lymphocytosis (MBL) is defined as asymptomatic monoclonal B-cell expansion characterised by a CLL-phenotype, but with less than 5 × 109…”
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Chronic lymphocytic leukemia with isochromosome 17q: An aggressive subgroup associated with TP53 mutations and complex karyotypes by Collado, Rosa, Puiggros, Anna, López-Guerrero, José Antonio, Calasanz, Ma José, Larráyoz, Ma José, Ivars, David, García-Casado, Zaida, Abella, Eugènia, Orero, Ma Teresa, Talavera, Elisabet, Oliveira, Ana Carla, Hernández-Rivas, Jesús Ma, Hernández-Sánchez, María, Luño, Elisa, Valiente, Alberto, Grau, Javier, Portal, Inmaculada, Gardella, Santiago, Salgado, Anna Camino, Giménez, Ma Teresa, Ardanaz, Ma Teresa, Campeny, Andrea, Hernández, José Julio, Álvarez, Sara, Espinet, Blanca, Carbonell, Félix

“…Although i(17q) [i(17q)] is frequently detected in hematological malignancies, few studies have assessed its clinical role in chronic lymphocytic leukemia…”
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A two-step approach for sequencing spliceosome-related genes as a complementary diagnostic assay in MDS patients with ringed sideroblasts by Janusz, Kamila, del Rey, Mónica, Abáigar, María, Collado, Rosa, Ivars, David, Hernández-Sánchez, María, Valiente, Alberto, Robledo, Cristina, Benito, Rocío, Díez-Campelo, María, Ramos, Fernando, Kohlmann, Alexander, Cañizo, Consuelo del, Hernández-Rivas, Jesús María

“…Highlights • Mutations in spliceosome-related genes in 94.3% of MDS-RS. • Presence of double mutations in the splicing machinery genes. • Good prognosis of…”
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Impact of azacitidine on red blood cell alloimmunisation in myelodysplastic syndrome by Ortiz, Sebastián, Orero, Maria T, Javier, Karla, Villegas, Carolina, Luna, Irene, Pérez, Pedro, Roig, Mónica, López, María, Costa, Sofía, Carbonell, Félix, Collado, Rosa, Ivars, David, Linares, Mariano

“…The incidence of alloimmunisation in myelodysplastic syndromes (MDS) during the era of supportive treatment ranges from 9 to 56%. However, it is unknown if the…”
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Increased Oxidative Damage Associated with Unfavorable Cytogenetic Subgroups in Chronic Lymphocytic Leukemia by Collado, Rosa, Ivars, David, Oliver, Isabel, Tormos, Carmen, Egea, Mercedes, Miguel, Amparo, Sáez, Guillermo T., Carbonell, Félix

“…Oxidative stress contributes to genomic instability in chronic lymphocytic leukemia (CLL), but its relationship with the acquisition of specific chromosomal…”
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Chromosome 8 Abnormalities (8p Losses and 8q Gains) in Patients with Chronic Lymphocytic Leukemia (CLL) and Del(17p) by Blanco, Gonzalo, Puiggros, Anna, Rodríguez-Rivera, María, Melero, Carme, García-Malo, María Dolores, Collado, Rosa, Ortega, Margarita, Calasanz, María José, Luño, Elisa, Vargas, María Teresa, Grau, Javier, Martínez-Laperche, Carolina, Valiente, Alberto, Cervera, José, Piñán, Ángeles, Hernández-Rivas, Jose María, Batlle, Ana, Salido, Marta, Ortuño, Francisco, Ardanaz, MªTeresa, Ferrer, Ana, Ivars, David, Rodriguez, Alicia, Abrisqueta, Pau, Espinet, Blanca

“…Basis. Abnormalities in chromosome 8 (8p-/8q+) are observed in 2-5% of CLL patients. Microarray studies have revealed up to 30-40% of 8 alterations in del(17p)…”
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Clinical and Biological Characterization of Patients with Low/Intermediate-1 Risk Myelodysplastic Syndrome and Iron Overload by Ivars, David, Collado, Rosa, Alguero, Carmen, Tormos, M Carmen, Diaz, Laura, Garcia-Gimenez, Jose Luis, Arrizabalaga, Beatriz, Orero, Mayte, Perez, Pedro, Sanchez, Magdalena, Ruiz, M Angeles, Yagüe, Nuria, Sancho-Tello, Reyes, Regadera, Ana, Tormo, Mar, Egea, Mercedes, Vidal, Elena, O'Connor, J Enrique, Saez, Guillermo T, Carbonell, Felix

“…Abstract 4956 Patients with Myelodysplastic Syndrome (MDS) are susceptible to developing iron overload as a response to the red blood cell (RBC) transfusions…”
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Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: Does −7/7q− detection by FISH have prognostic value? by Ademà, Vera, Hernández, Jesús María, Abáigar, María, Lumbreras, Eva, Such, Esperanza, Calull, Anna, Dominguez, Esther, Arenillas, Leonor, Mallo, Mar, Cervera, José, Marugán, Isabel, Tormo, Mar, García, Francisca, González, Teresa, Luño, Elisa, Sanzo, Carmen, Martín, María Luisa, Fernández, Manuela, Costa, Dolors, Blázquez, Beatriz, Barreña, Beatriz, Marco, Fernando, Batlle, Ana, Buño, Ismael, Martínez-Laperche, Carolina, Noriega, Víctor, Collado, Rosa, Ivars, David, Carbonell, Félix, Vallcorba, Isabel, Melero, Josefa, Delgado, Elena, Vargas, María Teresa, Grau, Javier, Salido, Marta, Espinet, Blanca, Melero, Carme, Florensa, Lourdes, Pedro, Carmen, Solé, Francesc

“…Abstract Chromosomal abnormalities are detected in 40–60% of patients with de novo myelodysplastic syndromes (MDS). This study used the FISH technique in 773…”
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