Professor, Ophthalmology, Northwestern University Medical School
Ophthalmology
Dr. Marilyn Mets, MD
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Marilyn Mets works in the field of Ophthalmology. She graduated from George Washington University School of Medicine. George Washington University School of Medicine has a rank of 67 in research and a 0 in primary care She has 5 awards "America's Top Doctors", "Chicago Magazine: Top Doctors", "Top MD", "Super Doctor" and "Fellow (FAAO)". Doctor Marilyn Mets, MD is a published doctor and has 86 publications published. The lastest was: 'Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.'
Publications
- The Effect of Amblyopia on Visual-Auditory Speech Perception: Why Mothers May Say "Look At Me When I'm Talking To You"
- Reversible nyctalopia and retinopathy in a patient with metastatic cancer treated with anti-heat shock protein 90 therapy.
- MicroRNAs-449a and -449b exhibit tumor suppressive effects in retinoblastoma.
- Usher Syndrome: Characteristics and Outcomes of Pediatric Cochlear Implant Recipients.
- Differentially expressed miRNAs in retinoblastoma.
- Contact lenses in the management of myopic anisometropic amblyopia.
- Phenotypes and functions of lymphocytes in congenital toxoplasmosis.
- Tonic upgaze in infancy.
- Natural history of optic pathway Tumors in children with neurofibromatosis type 1: a longitudinal study.
- Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
- Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.
- Early and longitudinal evaluations of treated infants and children and untreated historical patients with congenital toxoplasmosis: the Chicago Collaborative Treatment...
- The child with congenital toxoplasmosis.
- Absence of sensorineural hearing loss in treated infants and children with congenital toxoplasmosis.
- Atypical persistence of tunica vasculosa lentis.
- Toxoplasmosis-associated neovascular lesions treated successfully with ranibizumab and antiParasitic therapy.
- Longitudinal study of new eye lesions in children with toxoplasmosis who were not treated during the first year of life.
- Management of high accommodative convergence/accommodation ratio Esotropia.
- Binocularity following surgical correction of strabismus in adults.
- Rhegmatogenous Retinal detachments in children: risk factors and surgical outcomes.
- Cataracts in congenital toxoplasmosis.
- Neisseria meningitidis endogenous Endophthalmitis presenting as anterior uveitis.
- Longitudinal study of new eye lesions in treated congenital toxoplasmosis.
- Outcomes of a two-drug chemotherapy regimen for intraocular retinoblastoma.
- Impact of Visual impairment on measures of cognitive function for children with congenital toxoplasmosis: implications for compensatory intervention strategies.
- Outcome of treatment for congenital toxoplasmosis, 1981-2004: the National Collaborative Chicago-Based, Congenital Toxoplasmosis Study.
- Crystalline retinopathy in primary hyperoxaluria.
- Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
- Anti-γ-enolase autoimmune retinopathy manifesting in early childhood.
- Congenital cataracts in two siblings with Wolfram syndrome.
- Imaging of congenital toxoplasmosis Macular scars with optical coherence tomography.
- Sudden dispersion of retinoblastoma shortly after initial chemotherapy treatment.
- Preventing corneal abrasions in critically ill children receiving neuromuscular blockade: a randomized, controlled trial.
- Ophthalmic outcomes after prenatal and postnatal treatment of congenital toxoplasmosis.
- Lymphocytic choriomeningitis virus: emerging fetal teratogen.
- Neural larva migrans caused by the raccoon roundworm Baylisascaris procyonis.
- When may the posterior capsule be preserved in pediatric intraocular lens surgery?
- Lymphocytic choriomeningitis virus: a new addition to the TORCH evaluation.
- Cornea and iris changes in congenital ectropion uvea after trabeculotomy.
- Congenital toxoplasmosis transmitted from an immunologically competent mother infected before conception.
- Eye manifestations of congenital toxoplasmosis.
- Early diagnosis of Usher syndrome in infants and children.
- Resolution of intracranial calcifications in infants with treated congenital toxoplasmosis.
- Necrotizing periorbital cellulitis.
- Bilateral diffuse iris nodular nevi. Clinical and histopathologic characterization.
- Neurologic and developmental outcome in treated congenital toxoplasmosis.
- Cochlear implants in young children with Usher's syndrome.
- Postnatal Retinal development as measured by the electroretinogram in premature infants.
- Normal endothelial cell density range in childhood.
- Cataract, hearing loss and hypercholesterolemia.
- Stiles-Crawford effect and color matching in Stargardt's Disease.
- The Wagner syndrome versus hereditary arthroophthalmopathy.
- Fenestrated sheen Macular dystrophy.
- Uveal colobomas and Klinefelter's syndrome.
- The eye and the chromosome.
- Probable autosomal dominant optic atrophy with hearing loss.
- Ocular deviation after Retinal detachment surgery.
- Leber's congenital amaurosis. Retrospective review of 43 cases and a new fundus finding in two cases.
- Anomalies of Retinal architecture in Aicardi syndrome.
- Hemorrhagic retinopathy following uncomplicated pediatric cataract extraction.
- Inheritance of congenital Esotropia.
- Ocular findings in partial trisomy 10q syndrome.
- Spatial frequency and orientation tuning of spatial Visual mechanisms in human albinos.
- Albino spatial vision as an instance of arrested Visual development.
- X-linked congenital stationary night blindness. Review and report of a family with hyperopia.
- Infantile glaucoma in Down's syndrome (trisomy 21).
- Human albinos can discriminate spatial frequency and phase as accurately as normal subjects.
- Bietti crystalline retinopathy and Juvenile retinoschisis in a family with a novel RS1 mutation.
- Eye manifestations of intrauterine infections.
- Spontaneous resolution of cytomegalovirus retinitis in an infant with congenital cytomegalovirus infection.
- Congenital lymphocytic choriomeningitis virus infection: decade of rediscovery.
- Early diagnosis of Usher syndrome in children.
- Histopathological features of ocular toxoplasmosis in the fetus and infant.
- Lymphocytic choriomeningitis virus Chorioretinitis mimicking ocular toxoplasmosis in two otherwise normal children.
- Lymphocytic choriomeningitis virus: an underdiagnosed cause of congenital Chorioretinitis.
- Childhood blindness and Visual loss: an assessment at two institutions including a "new" cause.
- Iridocorneal adhesions in patients with the Marfan syndrome.
- Lymphocytic choriomeningitis virus: pediatric pathogen and fetal teratogen.
- Ophthalmic disorders in children with Down syndrome.
- Microphthalmos with cyst and Edwards' syndrome.
- Trisomy 4q with morning glory disc anomaly.
- Eye manifestations of intrauterine infections and their impact on childhood blindness.
- The electroretinogram in children.
- The natural history of retinal Degeneration in association with cobalamin C (cbl C) disease.
- Eye findings of diffuse unilateral subacute neuroretinitis and multiple choroidal infiltrates associated with neural larva migrans due to Bbaylisascaris procyonis.
Schools
George Washington University School Of Medicine
Cleveland Clinic Foundation
National Chldns Hospital
Procedures Preformed
- Extraocular Muscle Surgery
Conditions Treated
- Chorioretinitis
- Diplopia
- Esotropia
- Exophoria
- View All
Doctors Specialties
- Ophthalmology
Accepted Insurances
Awards
- America's Top Doctors
- Chicago Magazine: Top Doctors
- Top MD
- Super Doctor
- Fellow (FAAO)
Education
-
Cleveland Clinic Foundation -
George Washington University School of Medicine
Hospital
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Lurie Children's Hospital of Chicago -
Northwestern Memorial Hospital -
Ann & Robert H. Lurie Children?
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