M. Mets

B. A. Haldi, M. Mets, Cynthia L. Beauchamp, 2004, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Longitudinal study of new eye lesions in treated congenital toxoplasmosis.

Annie F Kuo, R. McLeod, W. Mieler, 2008, Ophthalmology.

Outcome of treatment for congenital toxoplasmosis, 1981-2004: the National Collaborative Chicago-Based, Congenital Toxoplasmosis Study.

R. McLeod, P. Meier, T. Karrison, 2006, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Management Strategies of Ocular Abnormalities in Patients with Marfan Syndrome: Current Perspective

S. Ansari, H. Esfandiari, M. Mets, 2019, Journal of ophthalmic & vision research.

Biometry Characteristics in Adults and Children With Marfan Syndrome: From the Marfan Eye Consortium of Chicago.

I. Kassem, I. Maumenee, M. Mets, 2017, American journal of ophthalmology.

The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries

Z. J. Khan, Matthew W. Wilson, C. Strahlendorf, 2022, The Lancet. Global health.

Lymphocytic choriomeningitis virus: emerging fetal teratogen.

M. Mets, Cynthia L. Beauchamp, L. Barton, 2002, American journal of obstetrics and gynecology.

Lymphocytic choriomeningitis virus: a new addition to the TORCH evaluation.

R. Bechtel, K. Haught, M. Mets, 1997, Archives of ophthalmology.

Human albinos can discriminate spatial frequency and phase as accurately as normal subjects

H. Wilson, C. Yo, M. Mets, 1989, Vision Research.

Albino spatial vision as an instance of arrested visual development

H. Wilson, M. Mets, A. Kressel, 1988, Vision Research.

Lymphocytic choriomeningitis virus: an underdiagnosed cause of congenital chorioretinitis.

Ali S Khan, T. Ksiazek, T. Ksiazek, 2000, American journal of ophthalmology.

Childhood blindness and visual loss: an assessment at two institutions including a "new" cause.

M. Mets, 1999, Transactions of the American Ophthalmological Society.

Congenital lymphocytic choriomeningitis virus infection: decade of rediscovery.

M. Mets, L. Barton, 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Pediatric Nd:YAG laser capsulotomy in the operating room: review of 87 cases.

B. Rahmani, M. Mets, M. Kinori, 2019, International journal of ophthalmology.

Aplasia of the Optic Nerve: A Report of Seven Cases

Maura E. Ryan, B. Rahmani, M. Mets, 2019, Neuro-ophthalmology.

Cataract, hearing loss and hypercholesterolemia

P. Nucci, M. Mets, 1990, Acta ophthalmologica.

Comparative data on SD-OCT for the retinal nerve fiber layer and retinal macular thickness in a large cohort with Marfan syndrome

A. Fawzi, M. Durbin, I. Maumenee, 2017, Ophthalmic genetics.

Longitudinal study of new eye lesions in children with toxoplasmosis who were not treated during the first year of life.

Annie F Kuo, R. McLeod, W. Mieler, 2008, American journal of ophthalmology.

Toxoplasmosis-associated neovascular lesions treated successfully with ranibizumab and antiparasitic therapy.

R. McLeod, R. Jager, W. Mieler, 2008, Archives of ophthalmology.

Impact of Visual Impairment on Measures of Cognitive Function for Children With Congenital Toxoplasmosis: Implications for Compensatory Intervention Strategies

R. McLeod, P. Meier, T. Karrison, 2006, Pediatrics.

Resolution of intracranial calcifications in infants with treated congenital toxoplasmosis.

R. McLeod, P. Meier, J. Remington, 1996, Radiology.

Eye manifestations of congenital toxoplasmosis.

R. McLeod, P. Meier, J. Remington, 1996, American journal of ophthalmology.

Early and longitudinal evaluations of treated infants and children and untreated historical patients with congenital toxoplasmosis: the Chicago Collaborative Treatment Trial.

N. Roizen, M. Mets, J. McAuley, 1994, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Cataracts in congenital toxoplasmosis.

R. McLeod, W. Mieler, T. Karrison, 2007, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Ophthalmic outcomes after prenatal and postnatal treatment of congenital toxoplasmosis.

R. McLeod, A. Brézin, M. Mets, 2003, American journal of ophthalmology.

The child with congenital toxoplasmosis.

R. McLeod, P. Meier, T. Karrison, 2000, Current clinical topics in infectious diseases.

Congenital toxoplasmosis transmitted from an immunologically competent mother infected before conception.

R. McLeod, R. Dorfman, J. Remington, 1996, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Neurologic and developmental outcome in treated congenital toxoplasmosis.

R. McLeod, P. Meier, J. Remington, 1995, Pediatrics.

Congenital lymphocytic choriomeningitis virus-an underdiagnosed fetal teratogen.

M. Mets, M. Kinori, Sudhi P Kurup, 2017, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

The eye and the chromosome.

I. Maumenee, M. Mets, 1983, Survey of ophthalmology.

Chorioretinal lesions in mothers of children with congenital toxoplasmosis in the National Collaborative Chicago-based, Congenital Toxoplasmosis Study.

R. McLeod, W. Mieler, P. Meier, 2010, Scientia medica.

Sudden dispersion of retinoblastoma shortly after initial chemotherapy treatment.

M. Mets, P. Bryar, Divya Srikumaran, 2009, American journal of ophthalmology.

Early and Longitudinal Evaluations of Treated Infants and Children and Untreated Historical Patients with Congenital Toxoplasmosis: The Chicago Collaborative Treatment Trial

R. McLeod, Charles R. Brown, P. Meier, 1994 .

Absence of Sensorineural Hearing Loss in Treated Infants and Children with Congenital Toxoplasmosis

R. McLeod, N. Kraus, T. Mcgee, 1992, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Neural larva migrans caused by the raccoon roundworm Baylisascaris procyonis.

A. T. Davis, S. Shulman, P. Gavin, 2002, The Pediatric infectious disease journal.

Phenotypes and functions of lymphocytes in congenital toxoplasmosis.

R. McLeod, N. Roizen, M. Mets, 1990, The Journal of laboratory and clinical medicine.

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

K. Arnos, A. Pandya, M. Bitner-Glindzicz, 2011, American journal of medical genetics. Part A.

Rhegmatogenous retinal detachments in children: risk factors and surgical outcomes.

D. Weinberg, M. Greenwald, M. Mets, 2003, Ophthalmology.

Iridocorneal adhesions in patients with the Marfan syndrome.

M. Greenwald, M. Mets, M. Donohoe, 1999, Ophthalmic genetics.

Preventing corneal abrasions in critically ill children receiving neuromuscular blockade: A randomized, controlled trial

K. Gauvreau, D. Hunter, M. Curley, 2009, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Crystalline retinopathy in primary hyperoxaluria.

Omar S. Punjabi, M. Mets, K. Riaz, 2011, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Branch Retinal Artery Occlusion Caused by Toxoplasmosis in an Adolescent

M. Shapiro, D. Goldstein, M. Mets, 2012, Case Reports in Ophthalmology.

Normal endothelial cell density range in childhood.

R Brancato, M B Mets, S. Shevell, 1990, Archives of ophthalmology.

The Long-term Visual Outcomes of Primary Congenital Glaucoma

H. Esfandiari, B. Rahmani, M. Mets, 2020, Journal of ophthalmic & vision research.

Long-term surgical outcomes of ab externo trabeculotomy in the management of primary congenital glaucoma.

A. Tanna, H. Esfandiari, B. Rahmani, 2019, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Spontaneous resolution of cytomegalovirus retinitis in an infant with congenital cytomegalovirus infection.

M. Mets, A. Noffke, 2001, Retina.

Lymphocytic choriomeningitis virus chorioretinitis mimicking ocular toxoplasmosis in two otherwise normal children.

M. Saron, A. Brézin, M. Mets, 2000, American journal of ophthalmology.

Eye manifestations of intrauterine infections and their impact on childhood blindness.

M. Mets, M. S. Chhabra, 2008, Survey of ophthalmology.

When may the posterior capsule be preserved in pediatric intraocular lens surgery?

M. Greenwald, M. Mets, S. Basti, 2002, Ophthalmology.

Eye manifestations of congenital toxoplasmosis.

M B Mets, R. McLeod, P. Meier, 1996, American journal of ophthalmology.

Necrotizing periorbital cellulitis.

M. Mets, J. Pensler, O. Placik, 1993, Annals of plastic surgery.

Eye findings of diffuse unilateral subacute neuroretinitis and multiple choroidal infiltrates associated with neural larva migrans due to Bbaylisascaris procyonis.

A. T. Davis, S. Shulman, P. Gavin, 2003, American journal of ophthalmology.

Anti-γ-enolase autoimmune retinopathy manifesting in early childhood.

R. Kardon, J. Folk, E. Stone, 2010, Archives of ophthalmology.

Leber's congenital amaurosis. Retrospective review of 43 cases and a new fundus finding in two cases.

I. Maumenee, M. Mets, R. Schroeder, 1987, Archives of ophthalmology.

Bilateral diffuse iris nodular nevi. Clinical and histopathologic characterization.

M. Tso, M. Mets, M. Rosner, 1995, Ophthalmology.

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

S. Kraft, L. Anson-Cartwright, R. Weleber, 1989, Genomics.

Novel miRNA-31 and miRNA-200a-Mediated Regulation of Retinoblastoma Proliferation

Hongmei Jiang, Hanli Fan, Gang Feng, 2015, PloS one.

The electroretinogram in children

M. Mets, Reut Parness-Yossifon, 2008, Current opinion in ophthalmology.

Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.

C. Ober, R. Hegele, O. Suchowersky, 2013, American journal of human genetics.

Recessive TRAPPC 11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability

C. Ober, R. Hegele, O. Suchowersky, 2013 .

Global Retinoblastoma Presentation and Analysis by National Income Level

Ankoor S. Shah, Z. J. Khan, C. Strahlendorf, 2020, JAMA oncology.

Cornea and iris changes in congenital ectropion uvea after trabeculotomy.

M. Mets, K. D. Khorram, 1997, Ophthalmic surgery and lasers.

The Natural History of Retinal Degeneration in Association with Cobalamin C (cbl C) Disease

M. Mets, A. Schimel, 2006, Ophthalmic genetics.

Chronic Granulomatous Disease: an Updated Experience, with Emphasis on Newly Recognized Features

Boris Katz, S. Shulman, M. Mets, 2022, Journal of Clinical Immunology.

Ocular findings in partial trisomy 10q syndrome.

K. Szego, M. Mets, K. Neely, 1988, American journal of ophthalmology.

Tonic upgaze in infancy.

M. Mets, 1990, Archives of ophthalmology.

Usher Syndrome: Characteristics and Outcomes of Pediatric Cochlear Implant Recipients

N. Young, K. Jatana, M. Mets, 2013, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Outcomes of a two‐drug chemotherapy regimen for intraocular retinoblastoma

P. Zage, R. Seshadri, M. Greenwald, 2008, Pediatric blood & cancer.

The ophthalmic practice of the future.

J. Schuman, E. Chew, E. Buckley, 2012, Archives of ophthalmology.

The Wagner syndrome versus hereditary arthroophthalmopathy.

I. Maumenee, M. Mets, H. Stoll, 1982, Transactions of the American Ophthalmological Society.

Early diagnosis of Usher syndrome in infants and children.

T. Hain, N. Young, M. Mets, 1996, The American journal of otology.

Cochlear Implants in Young Children with Usher'S Syndrome

T. Hain, N. Young, M. Mets, 1995, The Annals of otology, rhinology & laryngology. Supplement.

Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutation.

P. Sieving, L. Jampol, E. Bingham, 2001, A M A Archives of Ophthalmology.

Trisomy 4q with morning glory disc anomaly.

P. Nucci, M. Mets, E. B. Gabianelli, 1990, Ophthalmic paediatrics and genetics.

Long-term Clinical Outcomes of Ahmed and Baerveldt Drainage Device Surgery for Pediatric Glaucoma Following Cataract Surgery

A. Tanna, H. Esfandiari, B. Rahmani, 2019, Journal of glaucoma.

Microphthalmos with cyst and Edwards' syndrome.

E. Abboud, M. Mets, C. Guterman, 1990, American journal of ophthalmology.

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.

G. Fishman, B. Koop, K. Boycott, 1998, Nature genetics.

Inheritance of congenital esotropia.

T H Beaty, I H Maumenee, A Alston, 1986, Transactions of the American Ophthalmological Society.

Ocular biometry and determinants of refractive error in a founder population of European ancestry

M. Mets, Reut Parness-Yossifon, Sarah M. Hilkert, 2018, Ophthalmic genetics.

Anomalies of retinal architecture in Aicardi syndrome.

R. Tripathi, M. Mets, E. Torczynski, 1986, Archives of ophthalmology.

Neisseria meningitidis endogenous endophthalmitis presenting as anterior uveitis.

M. Mets, A. Noble, M. S. Chhabra, 2007, Journal of pediatric ophthalmology and strabismus.

Ocular abnormalities in a patient with congenital disorder of glycosylation type Ig

H. Esfandiari, M. Mets, Sudhi P Kurup, 2019, Ophthalmic genetics.

Histopathological features of ocular toxoplasmosis in the fetus and infant.

F. Roberts, D. Ferguson, R. McLeod, 2001, Archives of ophthalmology.

Contact lenses in the management of myopic anisometropic amblyopia.

M. Mets, R. L. Price, 1981, American journal of ophthalmology.

Stereoacuity outcomes following surgical correction of the nonaccommodative component in partially accommodative esotropia.

M. Mets, Sudhi P Kurup, Heath W. Barto, 2018, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Correction to: Chronic Granulomatous Disease: an Updated Experience, with Emphasis on Newly Recognized Features

Boris Katz, M. Mets, Z. Oikonomopoulou, 2022, Journal of Clinical Immunology.

Pupillary manifestations of Marfan syndrome: from the Marfan eye consortium of Chicago

M. Mets, Sudhi P Kurup, H. Ralay Ranaivo, 2018, Ophthalmic genetics.

Retinal Disease in Marfan Syndrome: From the Marfan Eye Consortium of Chicago.

A. Fawzi, S. Rahmani, I. Maumenee, 2013, Ophthalmic surgery, lasers & imaging retina.

A case of blepharophimosis: Freeman Sheldon syndrome

B. Rahmani, M. Mets, H. Ralay Ranaivo, 2021, Ophthalmic Genetics.

Differentially expressed miRNAs in retinoblastoma.

M. Soares, D. Scholtens, N. Laurie, 2013, Gene.

X-linked congenital stationary night blindness. Review and report of a family with hyperopia.

V. Smith, M. Mets, M. Wendell, 1991, Archives of ophthalmology.