Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ana Eugenia Rodríguez-Vicente"'
Autor:
Jesús María Hernández-Sánchez, José María Bastida, Diego Alonso-López, Rocío Benito, José Ramón González-Porras, Javier De Las Rivas, Jesús María Hernández Rivas, Ana Eugenia Rodríguez-Vicente
Publikováno v:
Platelets, Vol 31, Iss 8, Pp 993-1000 (2020)
In the last years, the use of thrombopoietin receptor agonists (TPO-RA), eltrombopag and romiplostim, has improved the management of immune thrombocytopenia (ITP). Moreover, eltrombopag is also active in patients with aplastic anemia and myelodysplas
Externí odkaz:
https://doaj.org/article/1d058db6f211498e816e3ec8ee6e8695
Autor:
Inmaculada Serramito-Gómez, Kathryn M. Clarke, Ana Eugenia Rodríguez-Vicente, Julie E. McGimpsey, María Abáigar, Carlos Barranquero Díez, Rocío Benito, Lars Bullinger, Ken I. Mills, Jesús María Hernández Rivas
Publikováno v:
HemaSphere, Vol 5, Iss 3, p e541 (2021)
Externí odkaz:
https://doaj.org/article/85780076835943e3956a4a40756d5f73
Autor:
José Ángel Hernández, María Hernández-Sánchez, Ana Eugenia Rodríguez-Vicente, Vera Grossmann, Rosa Collado, Cecilia Heras, Anna Puiggros, Ana África Martín, Noemí Puig, Rocío Benito, Cristina Robledo, Julio Delgado, Teresa González, José Antonio Queizán, Josefina Galende, Ignacio de la Fuente, Guillermo Martín-Núñez, José María Alonso, Pau Abrisqueta, Elisa Luño, Isabel Marugán, Isabel González-Gascón, Francesc Bosch, Alexander Kohlmann, Marcos González, Blanca Espinet, Jesús María Hernández-Rivas, Grupo Cooperativo Español de Citogenética Hematológica (GCECGH) and Grupo Español de Leucemia Linfática Crónica (GELLC)
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0143073 (2015)
To analyze the impact of the 11q deleted (11q-) cells in CLL patients on the time to first therapy (TFT) and overall survival (OS), 2,493 patients with CLL were studied. 242 patients (9.7%) had 11q-. Fluorescence in situ hybridization (FISH) studies
Externí odkaz:
https://doaj.org/article/6572f0a44cbe4c42af91d0ad5ea4aa40
Autor:
Claudia Pérez‐Carretero, María Hernández‐Sánchez, Teresa González, Miguel Quijada‐Álamo, Marta Martín‐Izquierdo, Sandra Santos‐Mínguez, Cristina Miguel‐García, María‐Jesús Vidal, Alfonso García‐De‐Coca, Josefina Galende, Emilia Pardal, Carlos Aguilar, Manuel Vargas‐Pabón, Julio Dávila, Isabel Gascón‐Y‐Marín, José‐Ángel Hernández‐Rivas, Rocío Benito, Jesús‐María Hernández‐Rivas, Ana‐Eugenia Rodríguez‐Vicente
Publikováno v:
American Journal of Hematology. 97:903-914
Interstitial 14q32 deletions involving IGH gene are infrequent events in chronic lymphocytic leukemia (CLL), affecting less than 5% of patients. To date, little is known about their clinical impact and molecular underpinnings, and its mutational land
Autor:
Jesús María Hernández-Rivas, Diego Alonso López, Eva Lumbreras, María Abáigar, Beatriz Arrizabalaga, Ana A. Martín, Teresa González, María Díez-Campelo, Jesús María Hernández Sánchez, Sara Erquiaga, Mónica del Rey, Raquel de Paz, Ana Eugenia Rodríguez Vicente
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The iron chelator deferasirox is widely used in patients with iron overload. Patients with low-grade myelodysplastic syndromes (MDS) get transfusion dependency and need to be treated with deferasirox to avoid iron overload. Moreover, in some patients
Autor:
José María Bastida, María Jesús Vidal-Manceñido, Josefina Galende, Ana-Eugenia Rodríguez-Vicente, Jesús María Hernández-Rivas, Ignacio García-Tuñón, Marta Martín-Izquierdo, Jose Angel Hernandez-Rivas, Isabel González-Gascón y Marín, José Antonio Queizán, Alberto Rodríguez-Sánchez, Miguel Quijada-Álamo, José Luis Ordóñez, Verónica Alonso-Pérez, Carlos Aguilar, Rocío Benito, Claudia Pérez-Carretero, María Hernández-Sánchez
Publikováno v:
Blood Cancer Journal
Blood Cancer Journal, Vol 11, Iss 7, Pp 1-11 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Blood Cancer Journal, Vol 11, Iss 7, Pp 1-11 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
© The Author(s) 2021.
BIRC3 is monoallelically deleted in up to 80% of chronic lymphocytic leukemia (CLL) cases harboring del(11q). In addition, truncating mutations in the remaining allele of this gene can lead to BIRC3 biallelic inactivation,
BIRC3 is monoallelically deleted in up to 80% of chronic lymphocytic leukemia (CLL) cases harboring del(11q). In addition, truncating mutations in the remaining allele of this gene can lead to BIRC3 biallelic inactivation,
Autor:
Mónica del Rey, Jesús María Hernández-Rivas, Rocío Benito, Alfonso García de Coca, Ana‐Belén Herrero, Araceli Rubio-Martinez, Julio Dávila‐Valls, Helen Parker, Jonathan C. Strefford, Ana-Eugenia Rodríguez-Vicente, María Hernández-Sánchez, José‐Luis Ordóñez, Sandra Santos-Mínguez, Miguel Quijada-Álamo, Teresa González, J.M. Hernández-Sánchez, Claudia Pérez-Carretero, Jose Angel Hernandez-Rivas, Marta Martín-Izquierdo
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 2, Pp n/a-n/a (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Clinical and Translational Medicine
Digital.CSIC. Repositorio Institucional del CSIC
instname
Clinical and Translational Medicine
© 2021 The Authors.
[Background]: Several genetic alterations have been identified as driver events in chronic lymphocytic leukemia (CLL) pathogenesis and oncogenic evolution. Concurrent driver alterations usually coexist within the same tumora
[Background]: Several genetic alterations have been identified as driver events in chronic lymphocytic leukemia (CLL) pathogenesis and oncogenic evolution. Concurrent driver alterations usually coexist within the same tumora
Autor:
Isabel González-Gascón-Y-Marín, Ana-Eugenia Rodríguez-Vicente, Victoria Ramos-Ascanio, Miguel Quijada-Álamo, Jose Angel Hernandez-Rivas, María Hernández-Sánchez, Claudia Pérez-Carretero, Carolina Muñoz-Novas
Publikováno v:
E-Prints Complutense. Archivo Institucional de la UCM
instname
Cancers, Vol 13, Iss 1782, p 1782 (2021)
Cancers
instname
Cancers, Vol 13, Iss 1782, p 1782 (2021)
Cancers
© 2021 by the authors.
Chronic lymphocytic leukemia (CLL) is an extremely heterogeneous disease. With the advent of oral targeted agents (Tas) the treatment of CLL has undergone a revolution, which has been accompanied by an improvement in pati
Chronic lymphocytic leukemia (CLL) is an extremely heterogeneous disease. With the advent of oral targeted agents (Tas) the treatment of CLL has undergone a revolution, which has been accompanied by an improvement in pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acd9e4013cdf2dcf0742b322054c146d
https://eprints.ucm.es/id/eprint/70923/1/cancers-13-01782.pdf
https://eprints.ucm.es/id/eprint/70923/1/cancers-13-01782.pdf
Autor:
Jesús María Hernández-Rivas, Ana-Eugenia Rodríguez-Vicente, Cecilia Heras, María Hernández-Sánchez, Isabel González-Gascón y Marín, María Poza-Santaella, José-Ángel Hernández, Maria‐Stefania Infante, Carolina Muñoz-Novas, Karen Marín, Maria Angeles Foncillas
Publikováno v:
BioMed Research International
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
BioMed Research International, Vol 2018 (2018)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
BioMed Research International, Vol 2018 (2018)
Digital.CSIC. Repositorio Institucional del CSIC
instname
In recent years, new prognostic indexes (PIs) for chronic lymphocytic leukemia (CLL), which include clinical, biological, and genetic variables, have been validated, highlighting the MD Anderson Cancer Center prognostic index (MDACC PI), the CLL-inte
Autor:
Maria Luisa Bernal, Luis Rojas, Maria José Herrero Cervera, Ana M. Peiró, Ana Eugenia Rodríguez Vicente
Publikováno v:
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Research and innovation in personalized medicine (PM) are extensive and expanding, with several pharmacogenetic/pharmacogenomic (PGx) testing options currently available for a wide range of health problems. However, PGx-guided therapy faces many barr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd84fd4e68d5d342cdc89855cb781938
http://hdl.handle.net/10261/245022
http://hdl.handle.net/10261/245022