Results 11 to 20 of about 95,483 (206)

Neurologic Complications of Intrauterine Herpes Simplex Virus Infection

open access: yesPediatric Neurology Briefs, 2011
Three case reports of intrauterine herpes simplex virus infection (HSV) and 61 cases published between 1963 and 2009 are reviewed by researchers at Baylor College of Medicine, Houston, TX.
J Gordon Millichap
doaj   +1 more source

Retrospective Analysis of the Results and Causes of Penetrating Keratoplasty with Native Donor Material in a Multidisciplinary Hospital (Along the Example of MCOC Botkin Hospital)

open access: yesOftalʹmologiâ, 2023
Penetrating keratoplasty (PC) is an operation of choice for urgent and planned conditions of the pathologic cornea. Moscow City Ophthalmological  Center “Botkin Hospital” together with the Moscow Coordination Center for  Organ Donation) over the past ...
G. Sh. Arzhimatova   +3 more
doaj   +1 more source

Inadvertent trypan blue staining of posterior capsule during cataract surgery associated with Argentinian flag event [PDF]

open access: yes, 2016
Trypan blue is common in visualizing the anterior capsule during cataract surgery. Inadvertent staining of the posterior capsule during phacoemulsification is a rare complication and there are few reports in the literature.
Alapati, Neeti M   +3 more
core   +4 more sources

Impact of tafluprost and tafluprost/timolol on the thickness of the retina in the macular area

open access: yesРоссийский офтальмологический журнал, 2019
Prostaglandin analogues (PAs) are the drugs of choice in the treatment of primary open-angle glaucoma (POAG). However, they have pro-inflammatory properties and may cause macular edema. Tafluprost is the first PA to be free of preservatives. The efficacy
N. I. Kurysheva   +3 more
doaj   +1 more source

Downbeat nystagmus: aetiology and comorbidity in 117 patients [PDF]

open access: yes, 2008
Objectives: Downbeat nystagmus (DBN) is the most common form of acquired involuntary ocular oscillation overriding fixation. According to previous studies, the cause of DBN is unsolved in up to 44% of cases.
Brandt, Thomas   +3 more
core   +1 more source

2-YEAR EXPERIENCE OF CORNEAL COLLAGEN CROSSLINKING IN KERATOCONUS TREATMENT

open access: yesOftalʹmologiâ, 2015
Aim. To assess reliability, efficacy, and stability of corneal collagen crosslinking (CXL) results for stage I‑II keratoconus.Patients and methods. 2‑year (2012-2014) results of CXL were analyzed. CXL was performed on 20 eyes of 15 patients (13 men and 2
D. D. Dement’ev   +2 more
doaj   +1 more source

Pathogenetic Aspects of the Development and Course of Rhegmatogenous Retinal Detachment against the Background of Proliferative Vitreoretinopathy. Literature Review

open access: yesOftalʹmologiâ, 2023
Retinal detachment (RD) is the most serious problem of modern ophthalmology, often leading to a decrease or irreversible loss of visual functions. The literature review is devoted to the latest trends in the study of the mechanisms of development and ...
J. V. Kudryavtseva, A. N. Semyonov
doaj   +1 more source

From variome to phenome : pathogenesis, diagnosis and management of ectopic mineralization disorders [PDF]

open access: yes, 2015
Ectopic mineralization - inappropriate biomineralization in soft tissues - is a frequent finding in physiological aging processes and several common disorders, which can be associated with significant morbidity and mortality.
De Vilder, eva, Vanakker, Olivier
core   +2 more sources

Visual pathway function and structure in Wolfram syndrome: Patient age, variation and progression [PDF]

open access: yes, 2018
Background/aimsTo report alterations in visual acuity and visual pathway structure over an interval of 1–3 years in a cohort of children, adolescents and young adults who have Wolfram syndrome (WFS) and to describe the range of disease severity evident ...
Al-Lozi, Amal   +6 more
core   +2 more sources

Rare diseases leading to childhood Glaucoma. epidemiology, pathophysiogenesis, and management [PDF]

open access: yes, 2015
Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of
Abdolrahimzadeh, Solmaz   +5 more
core   +10 more sources

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