Hospital Universitario Central de Asturias -ko ikertzaileekin lankidetzan egindako argitalpenak (6)

2024

  1. PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family

    Arquivos Brasileiros de Oftalmologia, Vol. 87, Núm. 5

2022

  1. Estudio retrospectivo de implante secundario de lentes de fijación retroiridiana en pacientes sin soporte capsular: resultados funcionales y complicaciones

    Archivos de la Sociedad Española de Oftalmologia, Vol. 97, Núm. 6, pp. 317-322

2012

  1. Long-term evolution of idiopathic lamellar macular holes and macular pseudoholes

    Canadian Journal of Ophthalmology, Vol. 47, Núm. 5, pp. 442-447

2010

  1. Autosomal recessive retinitis pigmentosa with early macular affectation caused by premature truncation in PROM1

    Investigative Ophthalmology and Visual Science, Vol. 51, Núm. 5, pp. 2656-2663

  2. Comprehensive SNP-chip for retinitis pigmentosa-Leber congenital amaurosis diagnosis: New mutations and detection of mutational founder effects

    European Journal of Human Genetics, Vol. 18, Núm. 1, pp. 118-124

2009

  1. Identification of an intronic single-point mutation in RP2 as the cause of semidominant X-linked retinitis pigmentosa

    Investigative Ophthalmology and Visual Science, Vol. 50, Núm. 11, pp. 5107-5114