A5089915061- Sarcoma Diagnosis and Treatment
- Corneal surgery and disorders
- RNA Interference and Gene Delivery
- Body Image and Dysmorphia Studies
- Retinopathy of Prematurity Studies
- Lymphoma Diagnosis and Treatment
- Parasitic Diseases Research and Treatment
- Neonatal Health and Biochemistry
- Genomics and Chromatin Dynamics
- Glaucoma and retinal disorders
- Ophthalmology and Visual Impairment Studies
- Retinal and Optic Conditions
- Dermatological diseases and infestations
- Retinal Development and Disorders
- Lysosomal Storage Disorders Research
- Alcohol Consumption and Health Effects
- Ocular Diseases and Behçet’s Syndrome
- Neonatal Respiratory Health Research
- Drug-Induced Ocular Toxicity
- Alcoholism and Thiamine Deficiency
- Eosinophilic Disorders and Syndromes
- Intraocular Surgery and Lenses
University of Minnesota
2023-2025
University of Minnesota Medical Center
2023-2024
Horizon Therapeutics (United States)
2023
National Eye Institute
2023
Johns Hopkins University
2023
Georgetown University
2018
Purpose: To report rates of change and identify factors associated with late in refractive outcome after toric intraocular lens (IOL) implantation. Setting: Single-site study at the Minneapolis Veterans Affairs Health Care System, Minneapolis, MN, USA. Design: Retrospective cohort study. Methods: Study inclusion required uncomplicated posterior chamber Alcon SN6ATT IOL implantation from 2010 –2017 refractions 1 month 5 years surgery. Exclusion criteria were sulcus placement, subsequent or...
Purpose To investigate whether COVID-19 infection is a risk factor for incident ocular inflammatory disease.
A rare case of Thelazia californiensis ocular infestation was diagnosed and treated in an 11-month-old patient.The patient presented with a visual acuity 20/130 OU by Teller cards. Exam demonstrated white, mobile worm the inferomedial fornix right eye. The remainder exam otherwise normal. removed under anesthesia identified as Division Parasitic Diseases Malaria, at Centers for Disease Control Prevention.This demonstrates but important cause follicular conjunctivitis foreign bodies,...
Mucopolysaccharidosis I (MPS I) is a genetic disorder characterized by mutation in the gene for enzyme alpha-L- iduronidase, which results accumulation of glycosaminoglycans over time. Children with this will suffer from organ failure and cognitive defects if untreated. While bone marrow transplantation replacement therapy reduce symptoms, it still associated significant abnormal function. This particularly true central nervous system, where blood-brain barrier serves as to efficacy these...
Roston, Sydney R. BS; Carey, Andrew MDEditor(s): Avery, Robert DO; Golnik, Karl C. MD; Froment, Caroline MD, PhD; Wang, An-Guor MD Author Information