Results 1 to 10 of about 345 (159)

Biomechanical homeostasis in ocular diseases: A mini-review. [PDF]

open access: yesFront Public Health, 2023
Diabetes mellitus-induced hyperglycemia is responsible for multiple pathological ocular alternations from vasculopathy to biomechanical dyshomeostasis.
Cheng Y, Ren T, Wang N.
europepmc   +3 more sources

Primary congenital glaucoma presenting with infantile nystagmus: a case report [PDF]

open access: yesPediatric Emergency Medicine Journal
Acute-onset nystagmus in pediatric patients is a rare but concerning presentation encountered in emergency departments. The differential diagnosis for pediatric nystagmus is broad.
Tessa R Meyer   +3 more
doaj   +3 more sources

INFLUENCE OF RESECTION OF THE CERVICAL SYMPATHETICIN OPTIC-NERVE ATROPHY, HYDROPHTHALMOS AND EXOPHTHALMIC GOITER. [PDF]

open access: yesJAMA - Journal of the American Medical Association, 1904
I. SYMPATHETICECTOMY IN OPTIC-NERVE ATROPHY. History. —Excision of the cervical portion of the sympathetic nerve for the relief of optic-nerve atrophy was proposed and executed by the writer in 1899. (The date of the first operation was June 24.) Report of Cases.
James Moores Ball
exaly   +3 more sources

EYE ENUCLEATION IN EUROPEAN BISON. CLINICAL CASE

open access: yesВетеринарная патология, 2021
Indications for enucleation of the eye in animals, as a rule, include chronic endophthalmitis or panophthalmitis, glaucoma leading to hydrophthalmos and buphthalmos, glaucoma-related retinal and optic nerve damage, intraocular neoplasms, and trauma ...
P. V. Aksenova
doaj   +1 more source

Ultrasound biomicroscopy of the anterior segment in patients with primary congenital glaucoma: a review of the literature

open access: yesActa Ophthalmologica, Volume 100, Issue 6, Page 605-613, September 2022., 2022
Abstract Purpose Primary congenital glaucoma (PCG) is a form of childhood glaucoma caused by maldevelopment of the anterior chamber. Disease severity differs greatly amongst patients. Ultrasound biomicroscopy (UBM) is a non‐invasive technique that can visualize the anterior segment in infants in vivo.
Robin Janssens   +4 more
wiley   +1 more source

Loss to follow-up barriers in care for Cornea Ulcers and Glaucoma: A Scoping Review Protocol [PDF]

open access: yes, 2021
To cite data: Saylor, K., Hicks, PM., Kang, L., Stagg, BC. Newman-Casey, PA., Woodward, MA., Literature search files for Loss to follow-up barriers in care for Cornea Ulcers and Glaucoma: A Scoping Review [Data set].
Hicks, Patrice   +5 more
core   +1 more source

Lowe syndrome: report of five cases [PDF]

open access: yes, 2010
INTRODUCTION: Lowe Syndrome, or Oculocerebrorenal Dystrophy (OCRL), has a recessive inheritance linked to X chromosome. It presents cataracts and glaucoma, delay in neuropsychomotor development, cognitive deficits, and renal Fanconi syndrome.
Andrade, Maria Cristina de   +5 more
core   +3 more sources

Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome [PDF]

open access: yes, 2015
Three international nosologies have been proposed for the diagnosis of Marfan syndrome (MFS): the Berlin nosology in 1988; the Ghent nosology in 1996 (Ghent-1); and the revised Ghent nosology in 2010 (Ghent-2).
Bannas, Peter   +13 more
core   +2 more sources

A role for OCRL in glomerular function and disease [PDF]

open access: yes, 2019
Background: Lowe syndrome and Dent-2 disease are caused by mutations in the OCRL gene, which encodes for an inositol 5-phosphatase. The renal phenotype associated with OCRL mutations typically comprises a selective proximal tubulopathy, which can ...
Bierzynska, Agnieszka   +6 more
core   +4 more sources

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