Results 61 to 70 of about 534,538 (278)
Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos +5 more
wiley +1 more source
PharmaceuticsObjectives: Insulin plays a crucial role in neuronal survival and oxidative stress modulation, making it a potential therapeutic target. This study investigates the effects of insulin in combination with a mesenchymal cell-derived secretome in patients ...
Paolo Giuseppe Limoli +2 more
doaj +1 more source
Oil droplet cataracts can mimic retinal disease
American Journal of Ophthalmology Case Reports, 2022 Purpose: Oil Droplet Cataracts in adults is an elusive diagnosis for ophthalmologist. It is difficult to diagnose, and patients can suffer for years with increasingly debilitating symptoms for what is a surgically curable condition.
Abraham Ifrah, MS, Janet S. Sunness, MD
doaj +1 more source
Optic neuropathy and low vision. XVII Convegno Low Vision Academy. [PDF]
, 2016 Organizzatore, moderatore e relatore nel Corso monotematico: “Malattie demielinizzanti e coinvolgimento oculare: classificazione, eziopatogenesi, diagnosi e clinica”
NEBBIOSO, Marcella
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Establishing the Service Potential of Secondary Level Low Vision Clinics [PDF]
, 2011 Purpose. To determine the proportion of people with low vision who can be adequately managed at a secondary level low vision clinic where only low to moderate magnification low vision devices (LVDs) and basic rehabilitation services are provided. Methods.
Elaine Y. H. Wong +5 more
core +1 more source
Comparative Effectiveness and Safety of Inebilizumab Versus Rituximab in AQP4‐IgG‐Positive NMOSD
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Rituximab (anti‐CD20, RTX) and inebilizumab (anti‐CD19, INE) represent B‐cell‐depleting therapies used for aquaporin‐4 antibody‐positive (AQP4‐IgG+) neuromyelitis optica spectrum disorder (NMOSD); however, direct comparative evidence remains limited.
Jie Lin +11 more
wiley +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
Annals 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
Widesight - a project aimed at improving peripheral vision [Elektronisk resurs] [PDF]
, 2000 Our group of researchers from a variety of backgrounds has been investigating the possibility of improving vision for patients with central scotoma. So far, these patients have only been offered enlarging devices and training.
Gustafsson, Jörgen,, Lund University.
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Multi-disciplinary low vision care [PDF]
, 2001 Case reports for three patients with low vision due to different ocular diseases are presented. In each case, a different rehabilitation professional was the main provider of the low vision care needed to meet the patient’s goals. However, in all cases
Lovie-Kitchin, Jan E. +3 more
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Annals 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