Results 41 to 50 of about 63,524 (342)
Retinal and optic nerve degeneration in α-mannosidosis
Orphanet Journal of Rare Diseases, 2018 Background α-mannosidosis is a rare, autosomal-recessive, lysosomal storage disease caused by a deficient activity of α-mannosidase. Typical symptoms include intellectual, motor and hearing impairment, facial coarsening, and musculoskeletal abnormalities.
Juliane Matlach +5 more
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Frontiers 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
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Diplopia and eye movement disorders.
, 2004 Published ...
Danchaivijitr, C, Kennard, C
core +2 more sources
Vision problems following stroke: developing a best practice statement [PDF]
, 2015 An estimated 15 million people worldwide suffer a stroke each year, and in developed countries, survival is increasing. Of those who survive 30 days or more after their first event, many experience stroke-related vision and visual problems.
Stanley, Jennifer, Tolmie, Elizabeth
core +1 more source
Mitochondrial neurogastrointestinal encephalomyopathy: approaches to diagnosis and treatment [PDF]
, 2020 Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an ultra-rare disease caused by mutations in TYMP, the gene encoding for the enzyme thymidine phosphorylase.
Bax, BE
core +1 more source
A protocol to quantify cross-sectional and longitudinal differences in duction patterns
Frontiers in NeuroscienceCurrently, 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
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Differential profile of protein expression on human keratocytes treated with autologous serum and plasma rich in growth factors (PRGF) [PDF]
, 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
Eye Segmentation Method for Telehealth: Application to the Myasthenia Gravis Physical Examination
Sensors, 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
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Frontiers 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
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Diplopia After Coronary Revascularization
Acta 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
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