Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Óscar Fuster"'
Autor:
Eva Barragán, Pau Montesinos, Mireia Camos, Marcos González, Maria J. Calasanz, José Román-Gómez, Maria T. Gómez-Casares, Rosa Ayala, Javier López, Óscar Fuster, Dolors Colomer, Carmen Chillón, María J. Larrayoz, Pedro Sánchez-Godoy, José González-Campos, Félix Manso, Maria L. Amador, Edo Vellenga, Bob Lowenberg, Miguel A. Sanz
Publikováno v:
Haematologica, Vol 96, Iss 10 (2011)
Background Fms-like tyrosine kinase-3 (FLT3) gene mutations are frequent in acute promyelocytic leukemia but their prognostic value is not well established.Design and Methods We evaluated FLT3-internal tandem duplication and FLT3-D835 mutations in pa
Externí odkaz:
https://doaj.org/article/61645e85ddeb4ab1890368d26a4ce8fe
Publikováno v:
International Journal of Family & Community Medicine. 6:94-97
Hairy cell leukemia (HCL) is a relatively rare chronic B-cell malignancy that involves the bone marrow, spleen and peripheral blood. Monocytopenia could represent a clue for the suspicion of HCL with complete blood counts (CBCs) and careful assessmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49ec6c2c9e80d0326cd7e0fc1841edc0
https://doi.org/10.15406/ijfcm.2022.06.00271
https://doi.org/10.15406/ijfcm.2022.06.00271
Autor:
de Juan Jiménez, Inmaculada, Cardeñosa, Eva Esteban, Suela, Sarai Palanca, González, Eva Barragán, Trejo, Dolores Salas, Lluch, Oscar Fuster, Gilabert, Pascual Bolufer
Publikováno v:
In Clinica Chimica Acta 2011 412(7):578-582
Publikováno v:
In International Journal of Antimicrobial Agents November 2012 40(5):475-477
Autor:
Inés Gómez-Seguí, Dolors Sánchez-Izquierdo, Eva Barragán, Esperanza Such, Irene Luna, María López-Pavía, Mariam Ibáñez, Eva Villamón, Carmen Alonso, Iván Martín, Marta Llop, Sandra Dolz, Oscar Fuster, Pau Montesinos, Carolina Cañigral, Blanca Boluda, Claudia Salazar, Jose Cervera, Miguel A Sanz
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100245 (2014)
Acute promyelocytic leukemia (APL) is characterized by the t(15;17)(q22;q21), but additional chromosomal abnormalities (ACA) and other rearrangements can contribute in the development of the whole leukemic phenotype. We hypothesized that some ACA not
Externí odkaz:
https://doaj.org/article/38079d609c6f4593990562fca5b858ba
Autor:
Ana Valencia, José Cervera, Esperanza Such, Eva Barragán, Pascual Bolufer, Oscar Fuster, Rosa Collado, Jesús Martínez, Miguel A. Sanz
Publikováno v:
Advances in Hematology, Vol 2009 (2009)
The Philadelphia (Ph1) chromosome arising from the reciprocal t(9;22) translocation is found in more than 90% of chronic myeloid leukemia (CML) patients and results in the formation of the chimeric fusion gene BCR-ABL. However, a small proportion of
Externí odkaz:
https://doaj.org/article/1f134c0f13f44c348e7ea4c8130e99c3