Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Xabier Aguirre"'
Autor:
Asier Achurra, Xabier Aguirre, Lñaki Bergera, Alberto Fernández, Paz Martín, Jesús Sanz, José-Mª Vázquez-Reina, Francisco-Javier Villarroel
Publikováno v:
Memoria de Proyectos. :11-29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9d9c6ab1724a8c319121938758e98d9
https://doi.org/10.15581/023.3.38154
https://doi.org/10.15581/023.3.38154
Autor:
Cristina Jimenez, Joan Bladé, Laura Rosiñol, Inmaculada Rapado, Rafael Feito Alonso, Beatriz Sanchez-Vega, Joaquin Martinez-Lopez, Teresa Cedena, Santiago Barrio, Maria-Victoria Mateos, Xabier Aguirre, Ramón García-Sanz, Isabel Cuenca, Yanira Ruiz-Heredia, Carlos Enrique Montenegro Marín, Juan José Lahuerta, Rosa Ayala, Bruno Paiva, Jesus San Miguel
Publikováno v:
Blood. 128:3283-3283
INTRODUCTION Minimal residual disease (MRD) assessment is an essential prognosis factor in multiple myeloma (MM). In this way different high-sensitivity quantification methods are being developed and improved using molecular or flow-cytometry approac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a846dd2336393a9c90cffc8e5ff75e68
https://doi.org/10.1182/blood.v128.22.3283.3283
https://doi.org/10.1182/blood.v128.22.3283.3283
Autor:
Laura Rosiñol, Keith Stewart, Beatriz Sanchez-Vega, Esteban Braggio, Joaquin Martinez-Lopez, Jesús Martín, Joan Bladé, Inmaculada Rapado, Maria-Victoria Mateos, Mercedes Gironella, Rafael Martínez, Xabier Aguirre, Jaime Pérez de Oteyza, M Asuncion Echeveste, Enrique M. Ocio, Jesus San Miguel, Rosa Ayala, Jose Carlos Martinez-Avila, Albert Oriol, Juan José Lahuerta, Ramón García-Sanz, Yanira Ruiz-Heredia, Joan Bargay, Cristina Jimenez
Publikováno v:
Blood. 128:2078-2078
Next-generation sequencing (NGS) has revealed new insight into the complexity of clonal and subclonal architecture of multiple myeloma (MM). The introduction of targeted studies allows the detection of mutations with very low allele frequencies at af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a050722a7639a08a7b99acecc9281f8
https://doi.org/10.1182/blood.v128.22.2078.2078
https://doi.org/10.1182/blood.v128.22.2078.2078
Autor:
Olga García, Elisa Luño, Alberto Valiente, Jaime Pérez-Oteyza, Jesús María Hernández-Rivas, Rosa Collado, Xabier Aguirre, Leonor Arenillas, Francesc Solé, Sara Alvarez, Paula Gomez-Marzo, Eva Lumbreras, Mar Mallo, Teresa Vallespi, Vera Adema, Ismael Buño, Laura Palomo, Carolina Martínez-Laperche, Calasanz Maria Jose, Beatriz Blazquez, Larrayoz Maria Jose, Ana Vicente, José Cervera, Ana Patiño-García
Publikováno v:
ResearcherID
Web of Science
Web of Science
INTRODUCTION Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal myeloid stem cell disorders highly prevalent in elderly populations. MDS are characterized by inefficient hematopoiesis, peripheral blood (PB) cytopenias, and increased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2206466fcb7736b86d6d0a6db2654ae5
https://doi.org/10.1182/blood.v124.21.1910.1910
https://doi.org/10.1182/blood.v124.21.1910.1910