The W.H.E.E.L.S. Preschool Vision Screening Program's Initial Outcomes for 12,402 Children Screened Using the Plusoptix Photoscreener

door Couser, Natario L.
Gepubliceerd in Int Sch Res Notices (2014)

Botulinum Toxin A Treatment of Consecutive Esotropia in Children

door Couser, Natario L., Lambert, Scott R.
Gepubliceerd in 2012

The Washington Metropolitan Pediatric Vision Screening Quality Control Assessment

door Couser, Natario L., Smith-Marshall, Janine
Gepubliceerd in 2011

Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases

door Kumar, Virang, Couser, Natario L., Pandya, Arti
Gepubliceerd in Case Rep Ophthalmol Med (2020)

Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review

door Stingl, Cybil S., Jackson-Cook, Colleen, Couser, Natario L.
Gepubliceerd in Case Rep Pediatr (2020)

Augmented Hummelsheim procedure to treat complete abducens nerve palsy

door Couser, Natario L., Lenhart, Phoebe D., Hutchinson, Amy K.
Gepubliceerd in 2012

Ocular Manifestations of the NAA10-Related Syndrome

door Gupta, Angela S., Saif, Hind Al, Lent, Jennifer M., Couser, Natario L.
Gepubliceerd in Case Rep Genet (2019)

An Adult Loa loa Worm in the Upper Eyelid: An Atypical Presentation of Loiasis in the United States

door Rodriguez, Linnet, White, Julia Michelle, Richards, Nikisha Q., You, Alan X., Couser, Natario L.
Gepubliceerd in Case Rep Ophthalmol Med (2021)

Candida Species Lens Abscesses in Infants with a History of Neonatal Candida Sepsis

door Couser, Natario L., Hubbard, G. Baker, Lee, Lyndon B., Hutchinson, Amy K., Lambert, Scott R.
Gepubliceerd in 2013

Corrigendum to “Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review”

door Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.
Gepubliceerd in Case Rep Genet (2020)

Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review

door Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.
Gepubliceerd in Case Rep Genet (2020)

The Phenotype of Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1: Report and Review

door Couser, Natario L., Masood, Maheer M., Strande, Natasha T., Foreman, Ann Katherine M., Crooks, Kristy, Weck, Karen E., Lu, Mei, Wilhelmsen, Kirk C., Roche, Myra, Evans, James P., Berg, Jonathan S., Powell, Cynthia M.
Gepubliceerd in Am J Med Genet A (2015)