Results 51 to 60 of about 88,010 (311)

The neuro-ophthalmological examination.

open access: yes, 2011
The neuro-ophthalmological examination constitutes one of the most refined and exact components of the clinical examination, often allowing precise diagnosis and formulation of a treatment plan even within the compass of the first visit.
R. John Leigh   +2 more
core   +1 more source

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro   +6 more
wiley   +1 more source

Partial Vitrectomy in the Treatment of Asteroid Hyalosis

open access: yesOftalʹmologiâ
The article discusses the results of a comparative analysis of surgical treatment of patients with asteroid hyalosis and the presence of kataract or artificial lens.
A. A. Veselov   +9 more
doaj   +1 more source

Estudo do comportamento da PIO de 24 horas e frequência de glaucoma em pacientes com síndrome da apnéia obstrutiva do sono Study on 24 hours IOP study and glaucoma frequency in patients with obstructive sleep apnea syndrome

open access: yesRevista Brasileira de Oftalmologia, 2009
OBJETIVO: Determinar a frequência de glaucoma e avaliar o comportamento da pressão intraocular (PIO) de 24 horas em pacientes portadores da síndrome da apnéia obstrutiva do sono (SAOS).
Maria Rosa Bet de Moraes Silva   +1 more
doaj   +1 more source

Femto-LASIK after Deep Anterior Lamellar Keratoplasty to Correct Residual Astigmatism: A Long-Term Case Series Study

open access: yesMedicina, 2022
Purpose: To evaluate the long-term outcomes of femtosecond laser-assisted in situ keratomileusis (Femto-LASIK) to correct residual astigmatism after deep anterior lamellar keratoplasty (DALK).
Belén Alfonso-Bartolozzi   +4 more
doaj   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru   +13 more
wiley   +1 more source

Dry eye masky syndrome: degree of expression and possibilities of correction

open access: yesРоссийский офтальмологический журнал, 2022
To prevent the spread of COVID-19, to ensure the safety of ourselves and others, personal protective equipment — various types of masks — has firmly entered our daily lives.
S. I. Makogon   +3 more
doaj   +1 more source

Subclinical Optic Nerve Involvement in Radiologically Isolated Syndrome: Multimodal Detection and Diagnostic Impact

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We aimed to determine the frequency of subclinical optic nerve (ON) lesions using MRI, optical coherence tomography (OCT), and visual evoked potentials (VEP) in radiologically isolated syndrome (RIS), and to assess their diagnostic and prognostic significance.
Christine Lebrun‐Frenay   +13 more
wiley   +1 more source

Ophthalmological situation of the patients with chronic renal failure undergoing haemodialysis [PDF]

open access: yes, 2021
Introduction: Haemodialysis (HD) is the unique treatment modality for end stage chronic renal failure (ESCRF) patients. In these patients, refractive changes, dry eye, increased tear osmolarity, conjunctival calcium deposits, band keratopathy, corneal ...
Ulusoy, Mahmut Oğuz   +3 more
core   +1 more source

Ophthalmological Findings in Joubert Syndrome and Related Disorders

open access: yes, 2022
Joubert syndrome (JS) is a rare genetic condition characterized by congenital malformation of the mid-hindbrain, cerebellar ataxia, hypotonia, oculomotor apraxia, hypoplasia of the cerebellar vermis resulting in breathing defects, ataxia, and delayed ...
Francesca Granata   +23 more
core   +1 more source

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