Publicaciones en colaboración con investigadores/as de Instituto de Investigación Sanitaria Biogipuzkoa (19)

2023

  1. ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease

    Frontiers in Genetics, Vol. 14

  2. Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients

    Genes, Vol. 14, Núm. 8

2022

  1. Assessing the Utility and Patient Satisfaction of Virtual Retina Clinics During COVID-19 Pandemic

    Clinical Ophthalmology, Vol. 16, pp. 311-321

  2. Incidence and Risk Factors Affecting the Recurrence of Primary Retinal Detachment in a Tertiary Hospital in Spain

    Journal of Clinical Medicine, Vol. 11, Núm. 15

  3. Potential Tear Biomarkers for the Diagnosis of Parkinson’s Disease—A Pilot Study

    Proteomes, Vol. 10, Núm. 1

  4. Subretinal Injection Techniques for Retinal Disease: A Review

    Journal of Clinical Medicine, Vol. 11, Núm. 16

2021

  1. Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-y)

    Scientific Reports

  2. Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

    Scientific Reports, Vol. 11, Núm. 1

  3. Plasma Rich in Growth Factors (PRGF) Increases the Number of Retinal Müller Glia in Culture but Not the Survival of Retinal Neurons

    Frontiers in Pharmacology, Vol. 12

  4. The Effect of Plasma Rich in Growth Factors on Microglial Migration, Macroglial Gliosis and Proliferation, and Neuronal Survival

    Frontiers in Pharmacology, Vol. 12

2020

  1. Inhibition of microRNA 6937 delays photoreceptor and vision loss in a mouse model of retinitis pigmentosa

    Pharmaceutics, Vol. 12, Núm. 10, pp. 1-15

2019

  1. Author Correction: A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies (Scientific Reports, (2018), 8, 1, (15457), 10.1038/s41598-018-33810-3)

    Scientific Reports

2018

  1. A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies

    Scientific Reports, Vol. 8, Núm. 1

  2. Anterior and posterior capsule densitometry levels after femtosecond laser-assisted cataract surgery

    International Journal of Ophthalmology, Vol. 11, Núm. 4, pp. 623-628

2017

  1. High prevalence of mutations affecting the splicing process in a Spanish cohort with autosomal dominant retinitis pigmentosa

    Scientific Reports, Vol. 7

2016

  1. A Cost-Effective Mutation Screening Strategy for Inherited Retinal Dystrophies

    Ophthalmic Research, Vol. 56, Núm. 3, pp. 123-131

  2. Increased aquaporin 1 and 5 membrane expression in the lens epithelium of cataract patients

    Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1862, Núm. 10, pp. 2015-2021

2013

  1. Genetic high throughput screening in Retinitis Pigmentosa based on high resolution melting (HRM) analysis

    Experimental Eye Research, Vol. 116, pp. 386-394

2012

  1. Current mutation discovery approaches in Retinitis Pigmentosa

    Vision Research, Vol. 75, pp. 117-129