Results 81 to 90 of about 25,332 (224)

Síndrome de isquemia ocular: manifestaciones clínicas, diagnóstico y evolución tras el tratamiento

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba, 2019
Ocular ischemia syndrome is caused by ocular chronic hypoperfusion due to stenosis or occlusion of the ipsilateral common or internal carotid artery. We present the case of a 58-year-old male with recurrent unilateral amaurosis fugax, ophthalmological ...
Abel Alejandro Sanabria Sanchinel   +3 more
doaj   +1 more source

Using induced pluripotent stem cells to understand retinal ciliopathy disease mechanisms and develop therapies [PDF]

open access: yes, 2016
The photoreceptor cells in the retina have a highly specialised sensory cilium, the outer segment (OS), which is important for detecting light. Mutations in cilia-related genes often result in retinal degeneration.
Cheetham, ME   +6 more
core   +1 more source

Internal carotid artery thrombosis and its evolution documented by computed tomography angiography

open access: yesClinics and Practice, 2011
A case of a 79-year-old man, affected by persistent right eye blindness after multiple episodes of transient left hemiparesis and right eye amaurosis. Brain computed tomography (Angio CT) well documented right internal carotid artery (ICA) plaque with a ...
Silvia Olivato   +3 more
doaj   +1 more source

Assessing the painful, uninflamed eye in primary care [PDF]

open access: yes, 2015
We acknowledge the important contributions of Professor Amada J Lee, University of Aberdeen, Division of Statistics, for assistance with analysing the data from the patient survey.
Dick, Andrew   +2 more
core   +1 more source

From amaurosis fugax to asymptomatic bithalamic infarct [PDF]

open access: yes, 2018
Bilateral paramedian thalamic infarctions are usually associated with impaired consciousness, oculomotor disturbances and neuropsychological changes. A 44-year-old healthy woman presented with amaurosis fugax of the right eye immediately after a Valsalva
Emond, H., Landis, T., Perren, F.
core  

Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7 [PDF]

open access: yes, 2016
BackgroundThe reduced cost and improved efficiency of whole genome sequencing (WGS) is drastically improving the development of cats as biomedical models.
Alhaddad, Hasan   +8 more
core   +3 more sources

Comprehensive structure-function analysis of causative variants in retinal pigment epithelium specific 65 kDa protein associated Leber Congenital Amaurosis

open access: yesNon-coding RNA Research, 2019
A recent study published to screen RPE65 in 187 families with Leber Congenital Amaurosis (LCA) by Zilin Zhong in 2019. There are seven novel variants were identified in RPE65, which was associated with LCA, but among only five were missense mutations [(c.
Zainularifeen Abduljaleel
doaj   +1 more source

Translational Retinal Research and Therapies. [PDF]

open access: yes, 2018
The following review summarizes the state of the art in representative aspects of gene therapy/translational medicine and evolves from a symposium held at the School of Veterinary Medicine, University of Pennsylvania on November 16, 2017 honoring Dr ...
Aguirre, Gustavo D   +7 more
core   +1 more source

Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA

open access: yesMolecular Therapy: Nucleic Acids, 2018
Ocular gene therapy with recombinant adeno-associated virus (AAV) has shown vector-mediated gene augmentation to be safe and efficacious in the retina in one set of diseases (retinitis pigmentosa and Leber congenital amaurosis (LCA) caused by RPE65 ...
Scott J. Dooley   +5 more
doaj   +1 more source

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