Results 71 to 80 of about 69,648 (309)
Strabismic syndromes and syndromic strabismus - a brief review [PDF]
arXiv, 2015 Strabismus can be found in association with congenital heart diseases, for examples, in velocardiofacial (DiGeorge) syndrome, Down syndrome, mild dysmorphic features, in CHARGE association, Turner syndrome, Ullrich-Turner syndrome, cardiofaciocutaneous syndrome.1-4 Some types of strabismus is heritable (e.g.
arxiv
Heroin withdrawal as a possible cause of acute concomitant esotropia in adults [PDF]
, 2001 Aim: To report the possible effects of heroin withdrawal on binocular vision. Methods: To present a case series of patients in whom esotropia developed on cessation of heroin use.
Firth, A.Y.
core
Orthoptic status before and immediately after heroin detoxification [PDF]
, 2004 Aim: To determine whether changes in orthoptic status take place during withdrawal from heroin and/or methadone. Method: A prospective study of patients, using a repeated measures design, attending a 5 day naltrexone compressed opiate detoxification ...
Beaini, A.Y. +3 more
core +2 more sources
Veterinary Record Case Reports, EarlyView.Abstract This case report describes a 6‐year‐old, mixed‐breed dog presenting with a non‐healing superficial corneal ulcer in the left eye, 5 years after undergoing surgical correction of the prolapsed gland of the third eyelid (‘cherry eye’). The ulcer was initially misinterpreted as a spontaneous chronic corneal epithelial defect due to its ...
Lionel Sebbag
wiley +1 more source
An active efficient coding model of the optokinetic nystagmus [PDF]
arXiv, 2016 Optokinetic nystagmus (OKN) is an involuntary eye movement responsible for stabilizing retinal images in the presence of relative motion between an observer and the environment. Fully understanding the development of optokinetic nystagmus requires a neurally plausible computational model that accounts for the neural development and the behavior.
arxiv
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis. [PDF]
, 2011 We present the case of an 18-month-old boy with dysmorphic facial features, developmental delay, growth retardation, bilateral clubfeet, thrombocytopenia, and strabismus, whose array CGH analysis revealed concurrent de novo trisomy 10p11.22p15.3 and ...
Dipple, Katrina M +3 more
core +2 more sources
World Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.ABSTRACT Spasmodic dysphonia is a laryngeal dystonia that can present as adductor, abductor, or mixed types, with or without tremor. The etiology is not understood fully. Comprehensive evaluation is required to establish the diagnosis. Treatments include voice therapy, medications, botulinum toxin injection, laryngeal surgery, deep brain stimulation ...
Aaron J. Jaworek, Robert T. Sataloff
wiley +1 more source
Evaluation of Corneal Endothelium in Adolescents with Juvenile Glaucoma
Journal of Ophthalmology, 2015 Purpose. To evaluate the endothelial cell density (ECD) and central corneal thickness (CCT) in adolescents with juvenile open-angle glaucoma (JOAG) and ocular hypertension (OH) and to investigate the influence of topical antiglaucoma medications on ECD ...
Beata Urban +3 more
doaj +1 more source
Artificial Intelligence for Pediatric Ophthalmology [PDF]
arXiv, 2019 PURPOSE OF REVIEW: Despite the impressive results of recent artificial intelligence (AI) applications to general ophthalmology, comparatively less progress has been made toward solving problems in pediatric ophthalmology using similar techniques. This article discusses the unique needs of pediatric ophthalmology patients and how AI techniques can ...
arxiv
Genetic and environmental contributions to strabismus and phoria: Evidence from twins [PDF]
, 2009 The causes of manifest (strabismus) and latent (phoria) misalignment of the visual axes are incompletely understood. We calculated genetic and environmental contributions to strabismus based upon a critical review and quantitative meta-analysis of ...
Backus, Benjamin T., Wilmer, Jeremy B.
core +1 more source