Results 11 to 20 of about 311,762 (300)
Corneal Nerve Abnormalities in Painful Dry Eye Disease Patients
Biomedicines, 2021 Background: This study aimed to compare the corneal nerve structural abnormalities detected using in vivo confocal microscopy (IVCM) in patients with neuropathic corneal pain (NCP) secondary to primary meibomian gland dysfunction (MGD) or autoimmune dry ...
Adrian Guerrero-Moreno +8 more
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Eye Movement Abnormalities in Multiple Sclerosis: Pathogenesis, Modeling, and Treatment
Frontiers in Neurology, 2018 Multiple sclerosis (MS) commonly causes eye movement abnormalities that may have a significant impact on patients’ disability. Inflammatory demyelinating lesions, especially occurring in the posterior fossa, result in a wide range of disorders, spanning ...
Alessandro Serra +2 more
doaj +3 more sources
Genetic Dissection of the Drosophila Nervous System by means of Mosaics [PDF]
, 1970 Given a mutant having abnormal behavior, the anatomical domain responsible for the deficit may be identified by the use of genetic mosaicism. Individuals may be produced in which a portion of the body is mutant male while the rest is normal female.
Benzer, Seymour, Hotta, Yoshiki
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Comparison of eye movements in schizophrenia and autism spectrum disorder
Neuropsychopharmacology Reports, 2020 Aim Eye movement abnormalities are often associated with psychiatric illness. Subjects with either schizophrenia or autism spectrum disorder (ASD) have been reported to show eye movement abnormalities.
Tomoko Shiino +7 more
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Creativity, Eye-Movement Abnormalities, and Aesthetic Appreciation of Magritte’s Paintings
Brain Sciences, 2022 Dyslexic children have been shown to be more creative than their non-dyslexic counterparts. They have also been shown to have an abnormal oculomotor profile while viewing targets in free space, making vergence or saccadic eye movements while reading or ...
Lindsey M Ward, Zoi Kapoula
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Arquivos de Neuro-Psiquiatria, 2010 OBJECTIVE: To describe the central nervous system (CNS) alterations present in a sample of oculo-auriculo-vertebral spectrum (OAVS) patients, trying to correlate them with other clinical features.
Rafael Fabiano Machado Rosa +5 more
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Eye abnormalities in Fryns syndrome [PDF]
American Journal of Medical Genetics Part A, 2003 AbstractFryns syndrome is a rare, generally lethal, autosomal recessive multiple congenital anomaly (MCA) syndrome first described in 1979. Patients with the syndrome present with the classical findings of cloudy cornea, brain malformations, diaphragmatic defects, and distal limb deformities. Over 70 patients have been reported revealing a wide variety
Diane M, Pierson +2 more
openaire +2 more sources
Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers. [PDF]
, 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
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Traumatic Lens Dislocation in an Eye with Anterior Megalophthalmos
Case Reports in Ophthalmological Medicine, 2022 Anterior megalophthalmos is a rare, bilateral, nonprogressive, hereditary, congenital disorder characterized by the enlargement of all anterior segment structures of the eye, with megalocornea, iris atrophy, and zonular abnormalities. We report a case of
Huda AlGhadeer
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Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
BMC Biology, 2023 Background Microphthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in nature,
Justine M. Chee +34 more
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