Publicaciones (26) Publicaciones de MARTA GALDÓS IZTUETA

2023

  1. Brain Degeneration in Synucleinopathies Based on Analysis of Cognition and Other Nonmotor Features: A Multimodal Imaging Study

    Biomedicines, Vol. 11, Núm. 2

2022

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

    Proteomes, Vol. 10, Núm. 1

  2. Spatial characterization of the effect of age and sex on macular layer thicknesses and foveal pit morphology

    PLoS ONE, Vol. 17, Núm. 12 December

2021

  1. Foveal pit morphology characterization: A quantitative analysis of the key methodological steps

    Entropy, Vol. 23, Núm. 6

  2. Retinal Thickness Predicts the Risk of Cognitive Decline in Parkinson Disease

    Annals of Neurology, Vol. 89, Núm. 1, pp. 165-176

  3. Visual dysfunction is associated with cognitive impairment in Parkinson's disease

    Parkinsonism and Related Disorders, Vol. 92, pp. 22-25

2020

  1. Macular ganglion cell complex thinning in children with visual field defects due to central nervous system pathology

    Eye (Basingstoke), Vol. 34, Núm. 9, pp. 1570-1576

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

  2. HGF -rs12536657 and Ocular Biometric Parameters in Hyperopic Children, Emmetropic Adolescents, and Young Adults: A Multicenter Quantitative Trait Study

    Journal of Ophthalmology, Vol. 2019

  3. Parafoveal thinning of inner retina is associated with visual dysfunction in Lewy body diseases

    Movement Disorders, Vol. 34, Núm. 9, pp. 1315-1324

  4. Protocolos en neuro-oftalmología pediátrica

    Acta estrabológica: publicación oficial de la Sociedad Española de Estrabología, Pleóptica, Ortóptica, Visión Binocular, Reeducación y Rehabilitación Visual, Vol. 48, Núm. 2, pp. 165-180

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. Parental mosaicism in PAX6 causes intra-familial variability: Implications for genetic counseling of congenital aniridia and microphthalmia

    Frontiers in Genetics, Vol. 9, Núm. OCT

2015

  1. Metabolomics in non-arteritic anterior ischemic optic neuropathy patients by liquid chromatography–quadrupole time-of-flight mass spectrometry

    Metabolomics, Vol. 11, Núm. 2, pp. 468-476

  2. Retinal thickness measured by spectral-domain optical coherence tomography in eyes without retinal abnormalities: The beaver dam eye study

    American Journal of Ophthalmology

2014

  1. Multicenter macular ganglion cell analysis: Normative paediatric reference range

    Acta Ophthalmologica

2013

  1. Multicenter Spanish study of spectral-domain optical coherence tomography in normal children

    Acta Ophthalmologica, Vol. 91, Núm. 1

  2. Programa de cribado para la retinopatía del prematuro en España

    Archivos de la Sociedad Española de Oftalmologia, Vol. 88, Núm. 5, pp. 184-188

  3. Protocolo de tratamiento de la retinopatía del prematuro en España

    Archivos de la Sociedad Española de Oftalmologia, Vol. 88, Núm. 6, pp. 231-236

2012

  1. Morphology of retinal vessels in the optic disk in a Göttingen minipig experimental glaucoma model

    Veterinary Ophthalmology, Vol. 15, Núm. SUPPL.1, pp. 36-46