Results 111 to 120 of about 5,074 (270)

Fourth Cranial Nerve Palsy and Brown Syndrome: Two Interrelated Congenital Cranial Dysinnervation Disorders? [PDF]

open access: yes, 2018
Based on neuroimaging data showing absence of the trochlear nerve, congenital superior oblique palsy is now classified as a congenital cranial dysinnervation disorder.
Brodsky, Michael   +1 more
core  

The use of the Newcastle Control Score in the management of intermittent exotropia [PDF]

open access: green, 2006
Deborah Buck   +6 more
openalex   +1 more source

Improvement in distance stereoacuity following surgery for intermittent exotropia [PDF]

open access: green, 2007
Wendy Adams   +6 more
openalex   +1 more source

Self-Reported Findings of the Korean Intermittent Exotropia Multicenter Study Questionnaire [PDF]

open access: yes
Purpose: To determine subjective symptoms and medical history of patients with intermittent exotropia in a large study population. Methods: The Korean Intermittent Exotropia Multicenter Study (KIEMS) is a nationwide, observational, cross-sectional ...
Gye, HJ   +8 more
core   +1 more source

Refractive Error Development in Children with Intermittent Exotropia [PDF]

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul
Background and Objective: Intermittent exotropia is the most common type of outward deviation of the eye in childhood. The association between myopia refractive error and intermittent exotropia has been shown in very few studies. This study was conducted
F Senobari   +4 more
doaj  

Socio-demographic distribution and clinical profile of exotropia in India: Electronic medical records-driven big data analytics report

open access: yesIndian Journal of Ophthalmology
Purpose: To describe the demographics and clinical profile of exotropia from patient data obtained from a multi-tiered ophthalmology hospital network in India.
Sampada Kulkarni   +4 more
doaj   +1 more source

Whole-exome sequencing uncovers the genetic basis of hereditary concomitant exotropia in ten Chinese pedigrees

open access: yesBMC Medical Genomics
Purpose To explore possible pathogenic genes for concomitant exotropia using whole-exome sequencing. Methods In this study, 47 individuals from 10 concomitant exotropia (including intermittent exotropia and constant exotropia) pedigrees were enrolled ...
Wenhua Duan   +4 more
doaj   +1 more source

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