Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Marta, Santiago"'
Autor:
Pilar Solves, Ana Bataller, Ana Belén Gálvez, Pedro Asensi Cantó, Marta Santiago, María José Moreno, Inés Gómez-Seguí, Javier de la Rubia
Publikováno v:
Hemato, Vol 5, Iss 2, Pp 109-114 (2024)
Background: Selective IgA deficiency (IgA-D) has been historically considered a high-risk entity for developing allergic/anaphylactic reactions after blood transfusion (AATRs). However, it has been suggested that the IgA-D-related anaphylactic transf
Externí odkaz:
https://doaj.org/article/9e21afe870d144d0bb2a9c23bf699831
Autor:
José Vicente Gil, Alberto Miralles, Sandra de las Heras, Esperanza Such, Gayane Avetisyan, Álvaro Díaz-González, Marta Santiago, Carolina Fuentes, José María Fernández, Pilar Lloret, Irene Navarro, Pau Montesinos, Marta Llop, Eva Barragán
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Introduction: Acute lymphoblastic leukemia (ALL) is a prevalent childhood cancer with high cure rate, but poses a significant medical challenge in adults and relapsed patients. Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL) is a high-ri
Externí odkaz:
https://doaj.org/article/3a32d9f59b0341d4840faa5e7c3ee8d0
Autor:
Lucia Castilla, Jose Aspa, Jorge Martínez Nieto, Ángel Zúñiga Cabrera, Marta Santiago, Ana Garcia Feria, Josefa Esperanza Marco Buades, María Argüello Marina, Rosa María Ayala Diaz, Ricardo Sanchez, Rafael Del Orbe Barreto, Ana Lobo Olmedo, Julio Dávila-Valls, Sonia Martín-Pérez, Cristina Jativa Saez, Inés Hernández Rodriguez, Eduardo Salido, Valle Recasens, Lucía Guerrero Fernández, Maria Belén Moreno Risco, Ataulfo González Fernández, Montserrat Lopez Rubio
Publikováno v:
HemaSphere, Vol 7, p e6313050 (2023)
Externí odkaz:
https://doaj.org/article/eda95f35d3a94157acf2603bc7cba2c6
Autor:
Álvaro Díaz González, Gayane Avetisyan, Cristian Garcia-Ruiz, José Vicente Gil, Marta Santiago, Juan José Domínguez-García, Marta Llop, Eva Barragan, Maria Leonor Senent Peris, Javier DE LA Rubia, José Cervera, Esperanza Such
Publikováno v:
HemaSphere, Vol 7, p e8338249 (2023)
Externí odkaz:
https://doaj.org/article/3b8292ebcb154ed4a860dfb92a532b39
Autor:
Marta Santiago Romero
Publikováno v:
Talía, Vol 5 (2023)
El presente artículo pretende analizar el proyecto La autoficción frente al espejo de metodología transmedia que fue realizado entre los años 2018 y 2022. Dicho proyecto se plantea como un vehículo para analizar y acercarse a la dramaturgia actu
Externí odkaz:
https://doaj.org/article/df06cc1a6b2e464290691a115cbd7138
Autor:
Álvaro Díaz-González, Elvira Mora, Gayane Avetisyan, Santiago Furió, Rosalía De la Puerta, José Vicente Gil, Alessandro Liquori, Eva Villamón, Carmen García-Hernández, Marta Santiago, Cristian García-Ruiz, Marta Llop, Blanca Ferrer-Lores, Eva Barragán, Silvia García-Palomares, Empar Mayordomo, Irene Luna, Ana Vicente, Lourdes Cordón, Leonor Senent, Alberto Álvarez-Larrán, José Cervera, Javier De la Rubia, Juan Carlos Hernández-Boluda, Esperanza Such
Publikováno v:
Cancers, Vol 15, Iss 11, p 3039 (2023)
Cytogenetic assessment in myelofibrosis is essential for risk stratification and patient management. However, an informative karyotype is unavailable in a significant proportion of patients. Optical genome mapping (OGM) is a promising technique that
Externí odkaz:
https://doaj.org/article/fa5758d9140b48b5b6c6e6a95ce4868e
Autor:
Luis López-Fando, Marta Santiago, Mercedes Ruiz, Javier Casado Varela, Guillermo Celada Luis, Miguel Angel Bonillo, Bárbara Padilla-Fernández, David M. Castro-Díaz, Miguel Jiménez, Manuel Esteban, Salvador Arlandis
Publikováno v:
Continence, Vol 2, Iss , Pp 100026- (2022)
Introduction:: The 3-Day Bladder Diary (3dBD) has good feasibility, reliability and validity for the assessment of Lower Urinary Tract Symptoms (LUTS) in women. This study aims to evaluate the reliability of the first day of the 3dBD (fdBD) in the as
Externí odkaz:
https://doaj.org/article/0913c042fd934083bc5853d3ecef6f12
Publikováno v:
Cancers, Vol 15, Iss 5, p 1590 (2023)
Hereditary myeloid malignancy syndromes (HMMSs) are rare but are becoming increasingly significant in clinical practice. One of the most well-known syndromes within this group is GATA2 deficiency. The GATA2 gene encodes a zinc finger transcription fa
Externí odkaz:
https://doaj.org/article/5ce74ea0900e49c3b4ccacffca146764
Autor:
José Vicente Gil, Esperanza Such, Claudia Sargas, Javier Simarro, Alberto Miralles, Gema Pérez, Inmaculada de Juan, Sarai Palanca, Gayane Avetisyan, Marta Santiago, Carolina Fuentes, José María Fernández, Ana Isabel Vicente, Samuel Romero, Marta Llop, Eva Barragán
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4440 (2023)
The molecular landscape of acute lymphoblastic leukemia (ALL) is highly heterogeneous, and genetic lesions are clinically relevant for diagnosis, risk stratification, and treatment guidance. Next-generation sequencing (NGS) has become an essential to
Externí odkaz:
https://doaj.org/article/476dc8d186764a17a893d2f8236bf10e
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