- idUS
- Listar por autor
Listar por autor "Ponte-Zuñiga, Beatriz"
Mostrando ítems 1-6 de 6
-
Artículo
Clinical Outcomes after Surgical Resection Combined with Brachytherapy for Uveal Melanomas
Relimpio López, Isabel; Garrido Hermosilla, Antonio Manuel; Espejo, Francisco; Gessa Sorroche, María; Coca, Lourdes; Domínguez, Belen; Ponte-Zuñiga, Beatriz; Terrón, José Antonio (MDPI, 2022)Currently, brachytherapy is the most commonly used therapeutic approach for uveal melanomas. Surgical resection by means ...
-
Artículo
Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy
García Delgado, Ana Belén; Valdes Sanchez, Lourdes; Morillo Sánchez, María José; Ponte-Zuñiga, Beatriz; Díaz-Corrales, Francisco J.; Cerda Haynes, Berta de la (BMC, 2021-05-17)Mutations in the EYS gene are one of the major causes of autosomal recessive retinitis pigmentosa. EYS-retinopathy presents ...
-
Artículo
Generation of a human iPS cell line (CABi003-A) from a patient with age-related macular degeneration carrying the CFH Y402H polymorphism
García Delgado, Ana Belén; Calado, Sofía M.; Valdés Sánchez, Lourdes; Montero Sánchez, Adoración; Ponte-Zuñiga, Beatriz; De la Cerda, Berta; Bhattacharya, Shom Shanker; Díaz Corrales, Francisco Javier (Elsevier, 2019)Age-related macular degeneration (AMD) is the leading cause of adult blindness in developed countries and is characterized ...
-
Artículo
Generation of a human iPS cell line from a patient with retinitis pigmentosa due to EYS mutation
Calado, Sofía M.; García Delgado, Ana Belén; Cerda, Berta De la; Ponte-Zuñiga, Beatriz; Bhattacharya, Shomi S.; Díaz Corrales, Francisco Javier (Elsevier, 2018-11-16)Retinitis pigmentosa (RP) is an inherited retinal degenerative disease. Mutations in EYS have been associated with autosomal ...
-
Artículo
Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene
Cañibano-Hernández, Alberto; Valdes Sanchez, Lourdes; García Delgado, Ana Belén; Ponte-Zuñiga, Beatriz; Díaz-Corrales, Francisco J.; Cerda Haynes, Berta de la (Elsevier, 2021-05)Retinal dystrophies associated to mutations in the CRB1 gene comprise a wide array of clinical presentations. A blood ...
-
Artículo
Identification of a PROM1 mutation in a Spanish family with inherited retinal dystrophies
Llavero-Valero, Pilar; Morillo-Sánchez, María José; Bravo-Gil, Nereida; Jiménez, Manuel Ramos; Ponte-Zuñiga, Beatriz; López-Domínguez, Mireia; Antiñolo Gil, Guillermo; Rodríguez de la Rúa Franch, Enrique (Bentham Open, 2021)Background: We report a Spanish family, comprising an affected mother and daughter, respectively diagnosed with retinitis ...