Search Results - "M. Martín-Izquierdo"

P622: DOUBLE‐HIT TRAF3 DELETION AND MUTATION IDENTIFIED BY HIGH‐THROUGHPUT SEQUENCING DEFINE A NEW INDEPENDENT PROGNOSTIC FACTOR IN CHRONIC LYMPHOCYTIC LEUKEMIA by Perez‐Carretero, C., Hernández‐Sánchez, M., Quijada‐Álamo, M., González, T., Rodríguez‐Sánchez, A., Martín‐Izquierdo, M., Matías‐Martín, J., Rubio, A., Dávila, J., García de Coca, A., Galende, J., Jimenez‐Montero, P., Queizán, J.‐A., González‐Gascón y Marín, I., Hernández‐Rivas, J.‐Á., Benito, R., Hernández‐Rivas, J.‐M., Rodríguez‐Vicente, A.‐E.

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Ureteritis Cystica: Important Consideration in the Differential Diagnosis of Acute Renal Colic by B. Padilla-Fernández, FJ. Díaz-Alférez, M. Herrero-Polo, M. Martín-Izquierdo, JM. Silva-Abuín, MF. Lorenzo-Gómez

“…Ureteritis cystica is an uncommon cause of acute renal pain. The aetiology remains unclear and the diagnosis may be difficult to establish. We report the case…”
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P756: ALLOGENEIC STEM CELL TRANSPLANTATION IN MYELODYSPLASTIC SYNDROME/MYELOPROLIFERATIVE NEOPLASM (MDS/MPN) OVERLAP SYNDROMES. A SINGLE CENTER EXPERIENCE AND DISSECTION OF MUTATIONAL PROFILE by Avendaño Pita, A., Martín Izquierdo, M., Muntión Olave, S., Jímenez Solas, T., García Antúnez, M., Eva, L., Del Rey, M., Toribio Castelló, S., Yeguas Bermejo, A., González, T., Hernández‐Rivas, J. M., Martín López, A. Á., Cabrero, M., Pérez López, E., Cabero, A., Baile, M., Vázquez, L., López Corral, L., Sánchez‐Guijo, F., Caballero Barrigon, D., Cortés Rodríguez, M., Díez Campelo, M.

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Mutational and Clonal Dynamics During Progression from MDS to SAML by Whole-Exome and Targeted-Deep Sequencing by Martín Izquierdo, M, Abáigar, M, Hernández-Sánchez, J.M, Tamborero, D, Díez-Campelo, M, Hernández-Sánchez, M, Ramos, F, Megido, M, Aguilar, C, Lumbreras, E, Redondo-Guijo, A, Recio, I, Olivier, C, Benito, R, López-Bigas, N, del Cañizo, M.C, Hernández-Rivas, J.M

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PF357 A NOVEL REFINED PROGNOSTIC MODEL FOR CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS COMBINING IGH TRANSLOCATIONS AND NEXT‐GENERATION SEQUENCING by Pérez‐Carretero, C., Hernández‐Sánchez, M., González‐Martínez, T., Quijada‐Álamo, M., Martín‐Izquierdo, M., Hernández‐Sánchez, J.M., Santos‐Minguez, S., Vidal‐Manceñido, M.J., García‐Coca, A., Aguilar‐Franco, C., Vargas‐Pabon, M., Alonso‐Álvarez, S., Sierra‐Pacho, M., Rubio‐Martínez, A., Dávila‐Valls, J., Díaz‐Valdéz, J.R., Queizán‐Hernández, J.A., Hernández‐Rivas, J.A., Benito‐Sánchez, R., Rodríguez‐Vicente, A.E., Hernández‐Rivas, J.M.

“…Background: Chromosome 14q32 translocations involving the immunoglobulin heavy chain gene (IGH) are uncommon in chronic lymphocytic leukemia (CLL) patients…”
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PO-1156: The role of magnetic resonance imaging in prostate cancer by González Del Portillo, E., Gil Restrepo, C., Soria Carreras, P., Martín Izquierdo, M., Virseda Rodríguez, Á., García García, J., Gómez Veiga, F., Pérez Romasanta, L.A.

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Topic: AS04-MDS Biology and Pathogenesis/AS04i-Microenvironment and stem cell niche by Solas, T. Jiménez, Olave, S. Muntión, López, F., Herrera, R. Ortega, Izquierdo, M. Martín, Martínez, T. González, Janusz, K., Ezponda, T., Vilas, A., Alfonso, A., Prosper, F., Molero, A., Valcárcel, D., Sánchez-Guijo, F., Díez-Campelo, M.

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P36 - Topic: AS04-MDS Biology and Pathogenesis/AS04i-Microenvironment and stem cell niche: MESENCHYMAL STROMAL CELLS MAY ENHANCE RESIDUAL HEALTHY HAEMATOPOIESIS IN LOW-RISK MDS PATIENTS by Solas, T. Jiménez, Olave, S. Muntión, López, F., Herrera, R. Ortega, Izquierdo, M. Martín, Martínez, T. González, Janusz, K., Ezponda, T., Vilas, A., Alfonso, A., Prosper, F., Molero, A., Valcárcel, D., Sánchez-Guijo, F., Díez-Campelo, M.

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Topic: AS06-Prognosis/AS06a-Prognostic factors of outcome and risk assessment by Izquierdo, M. Martín, Díez-Campelo, M., Del Real, J. Sánchez, Sánchez, A. Hernández, Sánchez, J.M. Hernández, Janusz, K., López, F., Tormo, M., Megido, M., Olivier, C., Madinaveitia-Ochoa, A., Dávila, J., Sierra, M., Vargas, M., Mínguez, S. Santos, García, C. Miguel, Benito, R., Rivas, J.M. Hernández, Ramos, F., Abáigar, M.

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O20 - Topic: AS06-Prognosis/AS06a-Prognostic factors of outcome and risk assessment: INCORPORATION OF COHESIN MUTATIONAL DATA INTO CURRENT IPSS-R CLASSIFICATION REFINES THE PROGNOSTIC STRATIFICATION OF VERY LOW/LOW-RISK MYELODYSPLASTIC SYNDROMES by Izquierdo, M. Martín, Díez-Campelo, M., Del Real, J. Sánchez, Sánchez, A. Hernández, Sánchez, J.M. Hernández, Janusz, K., López, F., Tormo, M., Megido, M., Olivier, C., Madinaveitia-Ochoa, A., Dávila, J., Sierra, M., Vargas, M., Mínguez, S. Santos, García, C. Miguel, Benito, R., Rivas, J.M. Hernández, Ramos, F., Abáigar, M.

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TRAF3 alterations are frequent in del‐3′IGH chronic lymphocytic leukemia patients and define a specific subgroup with adverse clinical features by Pérez‐Carretero, Claudia, Hernández‐Sánchez, María, González, Teresa, Quijada‐Álamo, Miguel, Martín‐Izquierdo, Marta, Santos‐Mínguez, Sandra, Miguel‐García, Cristina, Vidal, María‐Jesús, García‐De‐Coca, Alfonso, Galende, Josefina, Pardal, Emilia, Aguilar, Carlos, Vargas‐Pabón, Manuel, Dávila, Julio, Gascón‐Y‐Marín, Isabel, Hernández‐Rivas, José‐Ángel, Benito, Rocío, Hernández‐Rivas, Jesús‐María, Rodríguez‐Vicente, Ana‐Eugenia

“…Interstitial 14q32 deletions involving IGH gene are infrequent events in chronic lymphocytic leukemia (CLL), affecting less than 5% of patients. To date,…”
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Telemonitorización con Claria-Sharesource en diálisis peritoneal durante la pandemia de COVID-19 by Martín-Izquierdo, Edduin M., García-Mendez, Isabel, Rodríguez-Álvarez, Carla, Alonso-Bethencourt, Alejandro, Macía-Heras, Manuel

“…Antecedentes/Objetivo: Describir el empleo de la herramienta de telemonitorización con Claria-Sharesource (CSS) durante el periodo de confinamiento por…”
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87 - Mutational and Clonal Dynamics During Progression from MDS to SAML by Whole-Exome and Targeted-Deep Sequencing by Martín Izquierdo, M., Abáigar, M., Hernández-Sánchez, J.M., Tamborero, D., Díez-Campelo, M., Hernández-Sánchez, M., Ramos, F., Megido, M., Aguilar, C., Lumbreras, E., Redondo-Guijo, A., Recio, I., Olivier, C., Benito, R., López-Bigas, N., del Cañizo, M.C., Hernández-Rivas, J.M.

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196 - Mutational Status of Mesenchymal Stem Cell in Myelodysplastic Syndromes Patients by Janusz, K., Muntion, S., Hernández-Sánchez, J.M., Izquierdo, M. Martín, Hernández-Sánchez, M., Abáigar, M., Robledo, C., López-Cadenas, F., del Rey, M., Caballero, J.C., Benito, R., Guijo, A. Redondo, Jimenez, T., Sánchez-Guijo, F., del Cañzo, C., Díez-Campelo, M., Hernández-Rivas, J.M.

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Mutational Status of Mesenchymal Stem Cell in Myelodysplastic Syndromes Patients by Janusz, K, Muntion, S, Hernández-Sánchez, J.M, Izquierdo, M. Martín, Hernández-Sánchez, M, Abáigar, M, Robledo, C, López-Cadenas, F, del Rey, M, Caballero, J.C, Benito, R, Guijo, A. Redondo, Jimenez, T, Sánchez-Guijo, F, del Cañzo, C, Díez-Campelo, M, Hernández-Rivas, J.M

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PB1654 COMPREHENSIVE AND SEQUENTIAL GENETIC ANALYSIS OF B‐CELL ALL REVEALS AN ARRAY OF CHANGES WITH A HIGH INCIDENCE OF TP53 MUTATIONS AND IKZF1 DELETIONS by Montaño, A., Forero‐Castro, M., Robledo, C., Coca, A. García‐de, Fuster, J. L., Heras, N., Olivier, C., Hernández‐Sánchez, M., Corchete‐Sánchez, L. A., Martín‐Izquierdo, M., Riesco, S., González, T., Ribera, J., Ribera, J. M., Benito, R., Hernández‐Rivas, J.M.

“…Background: B‐Cell Precursor Acute Lymphoblastic Leukemia (BCP‐ALL) is a disease with specific secondary genetic alterations such as mutations (eg…”
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S896 SYNTHETIC LETHAL EFFECTS OF DUAL BCR AND PARP INHIBITION IN PROLIFERATIVE DEL(11Q) CLL CELLS IN THE PRESENCE OF STROMAL STIMULATION by Quijada‐Álamo, M., Hernández‐Sánchez, M., Rodríguez‐Vicente, A.E., Martín‐Izquierdo, M., Hernández‐Sánchez, J.M., Bastida, J.M., González, T., Alonso‐Pérez, V., García‐Tuñón, I., Galende, J., Aguilar, C., Queizán, J.A., Vidal‐Manceñido, M.J., Benito, R., Ordóñez, J.L., Wu, C.J., Hernández‐Rivas, J.M.

“…Background: Loss of the long arm of chromosome 11, del(11q), is one of the most common alterations in CLL. ATM gene is mutated in the remaining allele in one…”
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MUTATIONS ON COHESIN COMPLEX ARE ASSOCIATED TO A POOR PROGNOSIS IN LOW-RISK MYELODYSPLASTIC SYNDROMES PATIENTS: PF533 by Martín-Izquierdo, M., López-Cadenas, F., del Real, Sánchez J., Hernández-Sánchez, A., Hernández-Sánchez, J. M., Janusz, K., Lumbreras, E., Díez-Campelo, M., Tormo, M., Megido, M., Olivier, C., Madinaveitia-Ochoa, A., Martín-Nuñez, G., Dávila, J., Aguilar, C., Rodríguez, J. N., Alonso, J. M., Sierra, M., Vargas, M., Santos-Mínguez, S., Miguel-García, C., Benito, R., Hernández-Rivas, J. M., Ramos, F., Abáigar, M.

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PB2080 ROLE OF SOMATIC MUTATIONS IN PATIENTS WITH HIGH‐RISK MYELODISPLASTIC SYNDROMES TREATED WITH INTENSIVE CHEMOTHERAPY by Caballero, J. C., Sánchez, J. M. Hernández, Abáigar, M., Cadenas, F. López, Janusz, K., Izquierdo, M. Martín, Robledo, C., Ramos, F., Chillón, C., Sierra, M., Dávila, J., Cuello, R., De Cabo, E., Zato, E., Rivas, J. M. Hernández, Del Cañizo, M. C., Campelo, M. Díez

“…Background: Next Generation Sequencing (NGS) identify somatic mutations in driver genes in up to 90% of patients with MDS. Intensive Chemotherapy (IC) is…”
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PF533 MUTATIONS ON COHESIN COMPLEX ARE ASSOCIATED TO A POOR PROGNOSIS IN LOW‐RISK MYELODYSPLASTIC SYNDROMES PATIENTS by Martín‐Izquierdo, M., López‐Cadenas, F., Sánchez del Real, J., Hernández‐Sánchez, A., Hernández‐Sánchez, J.M., Janusz, K., Lumbreras, E., Díez‐Campelo, M., Tormo, M., Megido, M., Olivier, C., Madinaveitia‐Ochoa, A., Martín‐Nuñez, G., Dávila, J., Aguilar, C., Rodríguez, J.N., Alonso, J.M., Sierra, M., Vargas, M., Santos‐Mínguez, S., Miguel‐García, C., Benito, R., Hernández‐Rivas, J.M., Ramos, F., Abáigar, M.

“…Background: Mutations in cohesin complex genes have been described commonly in several types of cancer, with an incidence of 8% in myeloid diseases and…”
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