Publicaciones en colaboración con investigadores/as de Universidad de Castilla-La Mancha (13)

2020

  1. CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix

    Human Genetics, Vol. 139, Núm. 10, pp. 1209-1231

  2. Cataract extraction in patients with primary congenital glaucoma

    European Journal of Ophthalmology, Vol. 30, Núm. 3, pp. 525-532

  3. Normative Database of Peripapillary Vessel Density Measured by Optical Coherence Tomography Angiography and Correlation Study

    Current Eye Research, Vol. 45, Núm. 11, pp. 1430-1437

  4. Normative database and determinants of macular vessel density measured by optical coherence tomography angiography

    Clinical and Experimental Ophthalmology, Vol. 48, Núm. 1, pp. 44-52

2019

  1. Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma

    PLoS ONE, Vol. 14, Núm. 1

2017

  1. ANALYSIS of AGE-RELATED CHOROIDAL LAYERS THINNING in HEALTHY EYES USING SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY

    Retina, Vol. 37, Núm. 7, pp. 1305-1313

  2. Systemic Effects of Repeated Intraocular Dexamethasone Intravitreal Implant in Diabetic Patients: A Retrospective Study

    Diabetes Therapy, Vol. 8, Núm. 5, pp. 1087-1096

2015

  1. Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: Transactivation and phenotypic variability

    PLoS ONE, Vol. 10, Núm. 3

  2. The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations

    MicroRNA (Shāriqah, United Arab Emirates), Vol. 4, Núm. 1, pp. 50-56

2013

  1. Null CYP1B1 genotypes in primary congenital and nondominant juvenile glaucoma

    Ophthalmology, Vol. 120, Núm. 4, pp. 716-723

2012

  1. Recent patents and developments in glaucoma biomarkers

    Recent Patents on Endocrine, Metabolic and Immune Drug Discovery, Vol. 6, Núm. 3, pp. 224-234

2011

  1. WDR36 and P53 gene variants and susceptibility to primary open-angle glaucoma: Analysis of gene-gene interactions

    Investigative Ophthalmology and Visual Science, Vol. 52, Núm. 11, pp. 8467-8478

2009

  1. CYP1B1 mutations in Spanish patients with primary congenital glaucoma: Phenotypic and functional variability

    Molecular Vision, Vol. 15, pp. 417-431