Publicacións nas que colabora con María José Blanco Teijeiro (9)

2010

  1. Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: Homology with the nmf28/nmf28 mice model

    Clinical Genetics

2008

  1. Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa

    British Journal of Ophthalmology, Vol. 92, Núm. 10, pp. 1419-1423

2007

  1. Complement Factor H**This work was supported by the Fondo de Investigaciones Sanitarias de España Network (grant no. C03-13 received from the Spanish government).

    Ophthalmology

2003

  1. Ultrasound biomicroscopic findings in a cavitary melanocytoma of the ciliary body

    Canadian Journal of Ophthalmology, Vol. 38, Núm. 6, pp. 501-503

1999

  1. Transthyretin-related amyloidosis affecting the vitreous: Genetic diagnosis and therapy in a case

    Annals of Ophthalmology - Glaucoma, Vol. 31, Núm. 4-5, pp. 266-268

1998

  1. 160Thr mutation in the rhodopsin gene associated with retinitis pigmentosa

    Human Heredity, Vol. 48, Núm. 5, pp. 237-240

  2. Estudio epidemiológico, clínico y genético (rodopsina y cromosoma X) de la retinosis pigmentaria en Galicia

    Estudio epidemiológico, clínico y genético (rodopsina y cromosoma X) de la retinosis pigmentaria en Galicia

  3. Linkage analysis in a large Spanish family with X-linked retinitis pigmentosa: Phenotype-genotype correlation

    Clinical Genetics, Vol. 54, Núm. 1, pp. 26-32

1996

  1. Polymorphism within the exon 1 of the rhodopsin gene in the galician population

    Investigative Ophthalmology and Visual Science, Vol. 37, Núm. 3