CARMEN DORA
MÉNDEZ HERNÁNDEZ
Profesora asociada de Ciencias de la Salud
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Instituto de Salud Carlos III
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Salud Carlos III (14)
2024
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The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease
International Journal of Molecular Sciences, Vol. 25, Núm. 11
2023
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Agreement between Five Experts and the Laguna ONhE Automatic Colourimetric Application Interpreting the Glaucomatous Aspect of the Optic Nerve
Journal of Clinical Medicine, Vol. 12, Núm. 17
2021
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Agreement between rebound (Icare ic200) and applanation tonometry (Perkins) in patients with primary congenital glaucoma
Acta Ophthalmologica, Vol. 99, Núm. 6, pp. 663-668
2020
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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
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Ocular vascular changes in mild alzheimer’s disease patients: Foveal avascular zone, choroidal thickness, and onh hemoglobin analysis
Journal of Personalized Medicine, Vol. 10, Núm. 4, pp. 1-13
2019
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Retinal nerve fiber layer thickness in children with primary congenital glaucoma measured by spectral domain optical coherence tomography
Journal of AAPOS, Vol. 23, Núm. 2, pp. 94.e1-94.e4
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Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
PLoS ONE, Vol. 14, Núm. 1
2018
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Intraocular pressure following intrastromal corneal ring segments
Acta Ophthalmologica
2017
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Measuring intraocular pressure in patients with keratoconus with and without intrastromal corneal ring segments
Journal of Glaucoma, Vol. 26, Núm. 1, pp. 71-76
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Preliminary study of the differences in optic nerve head hemoglobin measures between patients with and without childhood glaucoma
Journal of Pediatric Ophthalmology and Strabismus, Vol. 54, Núm. 6, pp. 387-394
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Tonometry after Intrastromal Corneal Ring Segments for Keratoconus
Optometry and Vision Science, Vol. 94, Núm. 10, pp. 986-992
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Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Scientific Reports, Vol. 7
2016
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Rare FOXC1 variants in congenital glaucoma: Identification of translation regulatory sequences
European Journal of Human Genetics, Vol. 24, Núm. 5, pp. 672-680
2015
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Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: Transactivation and phenotypic variability
PLoS ONE, Vol. 10, Núm. 3