Results 21 to 30 of about 345 (159)

Equine glaucoma [PDF]

open access: yes, 2013
Glaucoma is a group of eye diseases characterized by functional damage to the optic nerve and ganglion cells of the retina, usually due to a transient or permanent elevation in intraocular pressure (IOP).
REGNIER, Alain
core   +1 more source

Novel OCRL mutations in children with Lowe Syndrome [PDF]

open access: yes, 2020
Background: Lowe syndrome is a rare X-linked recessive hereditary disease caused by mutations of the OCRL gene, which encodes an inositol polyphosphate-5-phosphatase.
Ding J   +5 more
core  

“A Textbook on Ophthalmology” by Ι.L. Bistis, Athens, 1908 [PDF]

open access: yes, 2010
In 1908, John L. Bistis wrote a textbook on Ophthalmology in order to provide the students of Medicine of his time with the appropriate material and facilitate his teaching. The book is divided in two parts.
Christopoulou-Aletra, Helen   +2 more
core   +1 more source

Viral-Antibody Complexes in Canine Adenovirus Type I (CAV-1) Ocular Lesion: Leukocyte Chemotaxis and Enzyme Release [PDF]

open access: yes, 1975
Canine adenovirus-type 1 (CAV-1)-antibody complexes caused severe anterior uveitis with corneal edema ( blue eye ) when injected into the anterior chamber of normal dogs.
Aguirre, Gustavo D   +3 more
core   +1 more source

OCULAR FINDINGS IN SLOTH BEARS (MELURSUS URSINUS) RESCUED FROM THE DANCING BEAR TRADE IN INDIA [PDF]

open access: yes
The aim of this study was to descriptively characterize the ophthalmic findings identified in 43 adult sloth bears (Melursus ursinus) rescued from the dancing bear trade in India and examined at two sloth bear rehabilitation centers in Agra and ...
Arun, Attur Shanmugam   +8 more
core   +2 more sources

Corneal Changes Assessed Using Confocal Microscopy in Patients With Unilateral Buphthalmos [PDF]

open access: yes, 2020
Citation: Mahelková G, Filouš A, Odehnal M, Cendelín J. Corneal changes assessed using confocal microscopy in patients with unilateral buphthalmos. Invest Ophthalmol Vis Sci. 2013;54:4048-4053. DOI:10. 1167/iovs.12-11165 PURPOSE.
Aleš Filouš   +4 more
core  

Lowe Syndrome (Oculo-cerebro-renal Syndrome of Lowe): A Case Report from Eastern India [PDF]

open access: yes, 2014
Lowe syndrome (the oculocerebrorenal syndrome of Lowe, OCRL) is a rare X-linked recessive metabolic disorder that primarily affects eyes, kidneys and brain. It is caused by the deficiency of enzyme phosphatidylinositol 4, 5-bisphosphate 5-phosphatase.
Dipankar Das   +2 more
core  

Impaired neural development in a zebrafish model for Lowe syndrome [PDF]

open access: yes, 2011
Solid state NMR/Biophysical Organic ...
Alia, A.   +7 more
core   +2 more sources

A scoping review of patients' barriers to eye care for glaucoma and keratitis. [PDF]

open access: yesSurv Ophthalmol, 2023
Hicks PM   +7 more
europepmc   +1 more source

A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome [PDF]

open access: yes, 2013
Oculocerebrorenal syndrome, also known as Lowe syndrome, is an X-linked recessive disorder that predominantly affects males and is characterized by growth and mental retardation, congenital cataract and renal Fanconi syndrome.
Ali Kanık   +5 more
core   +1 more source

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