Listar por autor "Blay Albors, Pilar"

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Are We Overestimating the Penetrance of Mutations in SDHB?

Schiavi, Francesca; Milne, Roger L.; Anda Apiñániz, Emma; Blay Albors, Pilar; Castellano, Maurizio; Opocher, Giuseppe; Robledo Batanero, Mercedes; Cascón Soriano, Alberto (2010)
Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

Bellido, Fernando; Sowada, N.; Mur, P.; Valdés Mas, Rafael María; Balbín Felechosa, Milagros; Blay Albors, Pilar (2018)
Delayed onset perforating folliculitis associated with sorafenib

Batalla Cebey, Ana; Menéndez, Lucía; Blay Albors, Pilar; Curto Iglesias, J. R. (2014)
Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma

Centeno Ramos, Irene; Blay Albors, Pilar; Santamaría Ruiz de Azúa, Íñigo; Astudillo González, María Aurora; Sánchez Pitiot, Ana Gloria; García Osorio, Fernando; González Arriaga, Patricia; Iglesias Llaca, Fernando; Menéndez Rodríguez, María Primitiva; Tardón García, Adonina; Pérez Freije, José María; Balbín Felechosa, Milagros (BioMed Central, 2011)
Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Seguí, Nuria; Mina, L. B.; Lázaro, Conxi; Valdés Mas, Rafael María; Balbín Felechosa, Milagros; Blay Albors, Pilar; Suárez Puente, Xosé Antón (2015)
Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree

Fernández Martínez, Lorena; Villegas, José Antonio; Santamaría Ruiz de Azúa, Íñigo; Sánchez Pitiot, Ana Gloria; González Alvarado, María Marta; Fernández, Soledad; Torres, Héctor; Paredes, Ángeles; Blay Albors, Pilar; Balbín Felechosa, Milagros (2017)
Impact of the incorporation of tyrosine kinase inhibitor agents on the treatment of patients with a diagnosis of advanced renal cell carcinoma: study based on experience at the Hospital Universitario Central de Asturias

Muriel López, Carolina; Esteban González, Emilio; Corral Blanco, Norberto Octavio; Jiménez Fonseca, Paula; Luque Cabal, María; Berros Fombella, José Pablo; Fernández Pérez, Yolanda; Blay Albors, Pilar; Fra Rodríguez, Joaquín; Villanueva Palicio, Noemí; Fernández de Sanmamed Gutiérrez, Miguel; Pardo Coto, Pablo; Izquierdo Manuel, Marta; Viéitez de Prado, José María; Estrada Hernández, Enrique; Jiménez Lacave, Ángel (2010)
Resultados oncológicos y funcionales del tratamiento no quirúrgico comparado con el quirúrgico en los carcinomas epidermoides de orofaringe

Díaz Molina, Juan Pablo; Rodrigo Tapia, Juan Pablo; Álvarez Marcos, César Antonio; Blay Albors, Pilar; Rúa Calderón, Ángeles de la; Estrada Hernández, Enrique; Alonso Pantiga, José Ramón (2012)

Listar por autor "Blay Albors, Pilar"

Are We Overestimating the Penetrance of Mutations in SDHB? ﻿

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer ﻿

Delayed onset perforating folliculitis associated with sorafenib ﻿

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma ﻿

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair ﻿

Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree ﻿

Impact of the incorporation of tyrosine kinase inhibitor agents on the treatment of patients with a diagnosis of advanced renal cell carcinoma: study based on experience at the Hospital Universitario Central de Asturias ﻿

Resultados oncológicos y funcionales del tratamiento no quirúrgico comparado con el quirúrgico en los carcinomas epidermoides de orofaringe ﻿

Are We Overestimating the Penetrance of Mutations in SDHB?

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

Delayed onset perforating folliculitis associated with sorafenib

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree

Impact of the incorporation of tyrosine kinase inhibitor agents on the treatment of patients with a diagnosis of advanced renal cell carcinoma: study based on experience at the Hospital Universitario Central de Asturias

Resultados oncológicos y funcionales del tratamiento no quirúrgico comparado con el quirúrgico en los carcinomas epidermoides de orofaringe