Envíos recientes

Aviso: Si va a participar en la campaña de sexenios 2024, le recomendamos que deposite en UVaDoc de forma preferente las aportaciones que vaya a presentar a dicha convocatoria (opción Autoarchivo). El resto de sus publicaciones podrá subirlas al repositorio en cualquier otro momento. Gracias.

Mostrando ítems 1-5 de 84

A comparison of stem cell-related gene expression in the progenitor-rich limbal epithelium and the differentiating central corneal epithelium

Nieto Miguel, Teresa ; Calonge, Margarita ; De La Mata Sampedro, Ana ; López Paniagua, Marina ; Galindo de la Rosa, Sara ; de la Paz, María Fideliz; Corrales, Rosa María (2011)
Reduction in the risk of peripheral neuropathy and lower decrease in kidney function with metformin, linagliptin or their fixed-dose combination compared to placebo in prediabetes: a randomized controlled trial

Gabriel, Rafael; Boukichou Abdelkader, Nisa; Gilis-Januszewska, Aleksandra; Makrilakis, Konstantinos; Gómez Huelgas, Ricardo; Kamenov, Zdravko; Paulweber, Bernhard; Satman, Ilhan; Djordjevic, Predrag; Alkandari, Abdullah; Mitrakou, Asimina; Lalic, Nebojsa; Egido, Jesús; Más Fontao, Sebastián; Calvet, Jean Henri; Pastor Jimeno, José Carlos ; Lindström, Jaana; Lind, Marcus; Acosta, Tania; Silva, Luis; Tuomilehto, Jaakko (2023)
Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

Puertas Neyra, Kevin Louis; Coco Martín, Rosa María ; Hernández Rodríguez, Leticia Adriana; Gobelli, Dino Joaquin ; García Ferrer, Yenisey; Palma Vecino, Raicel; Tellería Orriols, Juan José ; Simarro Grande, María ; Fuente García, Miguel Ángel de la ; Fernández Bueno, Iván (2024-07-02)
Clinical and genetic characterization of patients with eye diseases included in the Spanish Rare Diseases Patient Registry

López de la Rosa, Alberto; Tellería Orriols, Juan José ; Posada de la Paz, Manuel; Hermosilla-Gimeno, Isabel M.; Rivas, Miren Agurtzane; Gilabert, Raul; Coco Martín, Rosa María (2024-06-13)
Protocolo de tratamiento del edema macular quístico asociado a retinosis pigmentaria y otras distrofias hereditarias de la retina

Català-Mora, J.; Santamaría Álvarez, J.F.; Kyriakou, D.; Alforja, S.; Barraso Rodrigo, M.; Blasco Palacio, P.B.; Casaroli-Marano, R.; Cobos Martín, E.; Coco Martín, Rosa María ; Esmerado, C.; García Tirado, A; García, P; Gómez-Benlloch, A; Rodriguez Fernandez, C.A.; Vilaplana Mira, F (2024-02)

Instituto Universitario de Oftalmobiología Aplicada (IOBA): Envíos recientes

A comparison of stem cell-related gene expression in the progenitor-rich limbal epithelium and the differentiating central corneal epithelium ﻿

Reduction in the risk of peripheral neuropathy and lower decrease in kidney function with metformin, linagliptin or their fixed-dose combination compared to placebo in prediabetes: a randomized controlled trial ﻿

Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes ﻿

Clinical and genetic characterization of patients with eye diseases included in the Spanish Rare Diseases Patient Registry ﻿

Protocolo de tratamiento del edema macular quístico asociado a retinosis pigmentaria y otras distrofias hereditarias de la retina ﻿

A comparison of stem cell-related gene expression in the progenitor-rich limbal epithelium and the differentiating central corneal epithelium

Reduction in the risk of peripheral neuropathy and lower decrease in kidney function with metformin, linagliptin or their fixed-dose combination compared to placebo in prediabetes: a randomized controlled trial

Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes

Clinical and genetic characterization of patients with eye diseases included in the Spanish Rare Diseases Patient Registry

Protocolo de tratamiento del edema macular quístico asociado a retinosis pigmentaria y otras distrofias hereditarias de la retina