Results 31 to 40 of about 22,247 (288)

Eye Segmentation Method for Telehealth: Application to the Myasthenia Gravis Physical Examination

open access: yesSensors, 2023
Due to the precautions put in place during the COVID-19 pandemic, utilization of telemedicine has increased quickly for patient care and clinical trials.
Quentin Lesport   +6 more
doaj   +1 more source

Differential profile of protein expression on human keratocytes treated with autologous serum and plasma rich in growth factors (PRGF) [PDF]

open access: yes, 2018
Purpose The main objective of this study is to compare the protein expression of human keratocytes treated with Plasma rich in growth factors (PRGF) or autologous serum (AS) and previously induced to myofibroblast by TGF-beta 1 treatment.
Anitua Aldekoa, Eduardo   +7 more
core   +5 more sources

A protocol to quantify cross-sectional and longitudinal differences in duction patterns

open access: yesFrontiers in Neuroscience
Currently, there is no established system for quantifying patterns of ocular ductions. This poses challenges in tracking the onset and evolution of ocular motility disorders, as current clinical methodologies rely on subjective observations of individual
Kevin T. Willeford   +2 more
doaj   +1 more source

Diplopia After Coronary Revascularization

open access: yesActa Médica Portuguesa, 2020
Percutaneous coronary intervention is a coronary revascularization procedure that may rarely result in thromboembolic events. Although infrequent, ophthalmological complications of percutaneous interventions include a wide range of clinical presentations,
Joana Braga   +3 more
doaj   +1 more source

Reading networks in children with dyslexia compared to children with ocular motility disturbances revealed by fMRI

open access: yesFrontiers in Human Neuroscience, 2014
Developmental dyslexia is a neurological disorder whose underlying biological and cognitive causes are still being investigated, a key point of great significance, because it will determine the best therapeutic approach to use.Using functional magnetic ...
Ibone eSaralegui   +6 more
doaj   +1 more source

Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports

open access: yesFrontiers in Pediatrics, 2021
Introduction: Congenital muscular torticollis (CMT) is the most common cause of torticollis in infants; other causes, including osseous, ocular, and central nervous system torticollis can easily be overlooked.
Min-Wook Kim   +5 more
doaj   +1 more source

Vergence Neural Pathways: A Systematic Narrative Literature Review. [PDF]

open access: yes, 2016
Research in the neural pathway for vergence is less understood in comparison to the other four visual eye movements. The aim of this study was to review the literature on vergence neural pathways and associated disorders.
Rowe, Fiona J, Searle, Annabelle
core   +1 more source

Linking neurogenesis, oligodendrogenesis, and myelination defects to neurodevelopmental disruption in primary mitochondrial disorders

open access: yesFEBS Letters, EarlyView.
Mitochondrial remodeling shapes neural and glial lineage progression by matching metabolic supply with demand. Elevated OXPHOS supports differentiation and myelin formation, while myelin compaction lowers mitochondrial dependence, revealing mitochondria as key drivers of developmental energy adaptation.
Sahitya Ranjan Biswas   +3 more
wiley   +1 more source

Ocular sequelae from the illicit use of class A drugs [PDF]

open access: yes, 2004
Aim: To highlight the changes that may take place in the visual system of the class A drug abuser. Methods: A literature review was carried out of ocular/visual sequelae of the more common class A drugs.
Firth, A.Y.
core  

Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers. [PDF]

open access: yes, 2016
PurposeWe present a case of bilateral extensive peripapillary myelinated retinal nerve fibers (MRNF) in an individual with Crouzon syndrome, an inherited form of craniosynostosis caused by overactivation of fibroblast growth factor receptor 2.
Akil, Handan   +5 more
core   +3 more sources

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