Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Vanessa, Segura"'
Autor:
Pablo Gargallo, Silvestre Oltra, Julia Balaguer, Honorio Barranco, Yania Yáñez, Vanessa Segura, Antonio Juan-Ribelles, Inés Calabria, Margarita Llavador, Victoria Castel, Adela Cañete
Publikováno v:
International Journal of Retina and Vitreous, Vol 7, Iss 1, Pp 1-6 (2021)
Abstract Background Patients with 13q-syndrome are at risk of retinoblastoma when the RB1 gene, located in the chromosomal band 13q14.2, is deleted. This syndrome is frequently associated with congenital malformations and developmental delay, althoug
Externí odkaz:
https://doaj.org/article/4854e37913d24021b79989892874bb73
Autor:
Vassilios Papadakis, Vanessa Segura, Massimo Conte, Dominique Plantaz, Andrea Di Cataldo, Gudrun Schleiermacher, Kate Wheeler, Jose D. Bermúdez, Shifra Ash, Bénédicte Brichard, Ruth Ladenstein, Valérie Combaret, Sabine Sarnacki, Anna Maria Fagnani, Claudio Granata, Adela Cañete
Publikováno v:
Cancers, Vol 14, Iss 16, p 4007 (2022)
Background: To assess whether expectant observation of infants ≤ 90 days old with small suprarenal masses (sSRMs) could avoid unnecessary surgery without impacting outcome. Methods: Infants ≤ 90 days with a ≤ 5 cm mass, without midline extensio
Externí odkaz:
https://doaj.org/article/8cf17913baeb4cc7b950838eec0b3758
Autor:
Pablo Gargallo, Jaime Font de Mora, Pablo Berlanga, Inés Calabria, Margarita Llavador, Laia Pedrola, Joaquín Panadero, Sandra Dolz, Ángel Zúñiga, Juan Silvestre Oltra, Paloma Escobar, Yania Yáñez, María José Aparisi, Marina Martinez-Matilla, Vanessa Segura, Carlos Esquembre, María Del Cañizo, María José Moreno, Catalina Márquez, Adela Cañete, Victoria Castel
Publikováno v:
Translational Medicine Communications, Vol 4, Iss 1, Pp 1-11 (2019)
Abstract Background Understanding pediatric cancer biology is a huge challenge in continuous development that is currently being implemented into the clinical practice thanks to the new high throughput technologies integrated by personalized medicine
Externí odkaz:
https://doaj.org/article/450f5e23d5b04eedb8440b7f871920b8
Autor:
Pablo Gargallo, Silvestre Oltra, Yania Yáñez, Antonio Juan-Ribelles, Inés Calabria, Vanessa Segura, Marián Lázaro, Julia Balaguer, Teresa Tormo, Sandra Dolz, José María Fernández, Carolina Fuentes, Bárbara Torres, Mara Andrés, María Tasso, Victoria Castel, Jaime Font de Mora, Adela Cañete
Publikováno v:
Cancers, Vol 13, Iss 21, p 5339 (2021)
Knowledge about genetic predisposition to pediatric cancer is constantly expanding. The categorization and clinical management of the best-known syndromes has been refined over the years. Meanwhile, new genes for pediatric cancer susceptibility are d
Externí odkaz:
https://doaj.org/article/a7f124bedf9f4451910c25d01f1eed0f
Autor:
Gladys G. Olivera, Andrea Urtasun, Luis Sendra, Salvador F. Aliño, Yania Yáñez, Vanessa Segura, Pablo Gargallo, Pablo Berlanga, Victoria Castel, Adela Cañete, María José Herrero
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 18, p 9815 (2021)
Pharmacogenetics is one of the cornerstones of Personalized Precision Medicine that needs to be implemented in the routine of our patients’ clinical management in order to tailor their therapies as much as possible, with the aim of maximizing effic
Externí odkaz:
https://doaj.org/article/a9d908f604834a96b61ab68f587d52cc
Autor:
Antonio Juan Ribelles, Pablo Gargallo, Pablo Berlanga, Vanessa Segura, Yania Yáñez, Bárbara Juan, Marta Salom, Margarita Llavador, Jaime Font de Mora, Victoria Castel, Adela Cañete
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 4, p 268 (2021)
Background: Bone and soft-tissue sarcomas represent 13% of all paediatric malignancies. International contributions to introduce next-generation sequencing (NGS) approaches into clinical application are currently developing. We present the results fr
Externí odkaz:
https://doaj.org/article/7766472dd96248638860e5f878e43c7e
Autor:
Pablo Gargallo, Silvestre Oltra, María Tasso, Julia Balaguer, Yania Yáñez, Sandra Dolz, Inés Calabria, Francisco Martínez, Vanessa Segura, Antonio Juan-Ribelles, Margarita Llavador, Victoria Castel, Adela Cañete, Jaime Font de Mora
Publikováno v:
EUROPEAN JOURNAL OF HUMAN GENETICS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
CTCF germline mutations have been related to MRD21. We report the first bilateral Wilms tumor suffered by a MRD21 patient carrying an unreported CTCF missense variant in a zinc finger domain of CTCF protein. We found that germline heterozygous varian
Autor:
Gladys G. Olivera, Yania Yáñez, Pablo Gargallo, Luis Sendra, Salvador F. Aliño, Vanessa Segura, Miguel Ángel Sanz, Adela Cañete, Victoria Castel, Jaime Font De Mora, David Hervás, Pablo Berlanga, María José Herrero
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 8, p 2714 (2020)
Single nucleotide polymorphisms (SNPs) in Pharmacogenetics can play an important role in the outcomes of the chemotherapy treatment in Neuroblastoma, helping doctors maximize efficacy and minimize toxicity. Employing AgenaBioscience MassArray, 96 SNP
Externí odkaz:
https://doaj.org/article/cf8f3fc0f20042af984058e4e6397564
Publikováno v:
Anales de Pediatría, Vol 90, Iss 1, Pp 54-55 (2019)
Externí odkaz:
https://doaj.org/article/e6965b0b93074314b3a16b48793bc0fc
Publikováno v:
Anales de Pediatría (English Edition), Vol 90, Iss 1, Pp 54-55 (2019)
Externí odkaz:
https://doaj.org/article/e8bbb3a6c16b47b68093cc66c4e3d25a