Retinal, visual, and refractive development in retinopathy of prematurity

por Moskowitz, Anne, Hansen, Ronald M, Fulton, Anne B
Publicado 2016

Multifocal ERG Responses in Subjects With a History of Preterm Birth

por Altschwager, Pablo, Moskowitz, Anne, Fulton, Anne B., Hansen, Ronald M.
Publicado 2017

Increment Threshold Functions in Retinopathy of Prematurity

por Hansen, Ronald M., Moskowitz, Anne, Bush, Jennifer N., Fulton, Anne B.
Publicado 2016

The Development of Retinal Function and Refractive Error in Children With Retinopathy of Prematurity

por De Bruyn, Hanna, Hansen, Ronald M., Akula, James D., Fulton, Anne B.
Publicado 2023

High prevalence of strabismic visual field expansion in pediatric homonymous hemianopia

por Bronstad, P. Matthew, Peli, Eli, Liu, Rui, Doherty, Amy, Fulton, Anne B.
Publicado 2018

Non-Rigid Registration for High-Resolution Retinal Imaging

por Mujat, Mircea, Akula, James D., Fulton, Anne B., Ferguson, R. Daniel, Iftimia, Nicusor
Publicado 2023

Evaluation of the Relationship Between Preferential Looking Testing and Visual Evoked Potentials as a Biomarker of Cerebral Visual Impairment

por Raja, Sruti, Emadi, Batool Sahar, Gaier, Eric D., Gise, Ryan A., Fulton, Anne B., Heidary, Gena
Publicado 2021

A Simplified Model of Activation and Deactivation of Human Rod Phototransduction—An Electroretinographic Study

por Akula, James D., Lancos, Annie M., AlWattar, Bilal K., De Bruyn, Hanna, Hansen, Ronald M., Fulton, Anne B.
Publicado 2023

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

por Luo, Shiyu, Alwattar, Bilal, Li, Qifei, Bora, Kiran, Blomfield, Alexandra K., Lin, Jasmine, Fulton, Anne, Chen, Jing, Agrawal, Pankaj B.
Publicado 2023

The neurovascular relation in oxygen-induced retinopathy

por Akula, James D., Mocko, Julie A., Benador, Ilan Y., Hansen, Ronald M., Favazza, Tara L., Vyhovsky, Tanya C., Fulton, Anne B.
Publicado 2008

ISCEV guide to visual electrodiagnostic procedures

por Robson, Anthony G., Nilsson, Josefin, Li, Shiying, Jalali, Subhadra, Fulton, Anne B., Tormene, Alma Patrizia, Holder, Graham E., Brodie, Scott E.
Publicado 2018

The importance of genetic testing as demonstrated by two cases of CACNA1F-associated retinal generation misdiagnosed as LCA

por Men, Clara J., Bujakowska, Kinga M., Comander, Jason, Place, Emily, Bedoukian, Emma C., Zhu, Xiaosong, Leroy, Bart P., Fulton, Anne B., Pierce, Eric A.
Publicado 2017

The Fovea in Retinopathy of Prematurity

por Akula, James D., Arellano, Ivana A., Swanson, Emily A., Favazza, Tara L., Bowe, Theodore S., Munro, Robert J., Ferguson, R. Daniel, Hansen, Ronald M., Moskowitz, Anne, Fulton, Anne B.
Publicado 2020

Extrafoveal Cone Packing in Eyes With a History of Retinopathy of Prematurity

por Ramamirtham, Ramkumar, Akula, James D., Soni, Garima, Swanson, Matthew J., Bush, Jennifer N., Moskowitz, Anne, Swanson, Emily A., Favazza, Tara L., Tavormina, Jena L., Mujat, Mircea, Ferguson, R. Daniel, Hansen, Ronald M., Fulton, Anne B.
Publicado 2016

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

por Kruijt, Charlotte C., Gradstein, Libe, Bergen, Arthur A., Florijn, Ralph J., Arveiler, Benoit, Lasseaux, Eulalie, Zanlonghi, Xavier, Bagdonaite-Bejarano, Laura, Fulton, Anne B., Yahalom, Claudia, Blumenfeld, Anat, Perez, Yonatan, Birk, Ohad S., de Wit, Gerard C., Schalij-Delfos, Nicoline E., van Genderen, Maria M.
Publicado 2022

Panel-based Genetic Diagnostic Testing for Inherited Eye Diseases is Highly Accurate and Reproducible and More Sensitive for Variant Detection Than Exome Sequencing

por Consugar, Mark B., Navarro-Gomez, Daniel, Place, Emily M., Bujakowska, Kinga M., Sousa, Maria E., Fonseca-Kelly, Zoë D., Taub, Daniel G., Janessian, Maria, Wang, Dan Yi, Au, Elizabeth D., Sims, Katherine B., Sweetser, David A., Fulton, Anne B., Liu, Qin, Wiggs, Janey L., Gai, Xiaowu, Pierce, Eric A.
Publicado 2014

Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD

por Sangermano, Riccardo, Deitch, Iris, Peter, Virginie G., Ba-Abbad, Rola, Place, Emily M., Zampaglione, Erin, Wagner, Naomi E., Fulton, Anne B., Coutinho-Santos, Luisa, Rosin, Boris, Dunet, Vincent, AlTalbishi, Ala’a, Banin, Eyal, Sousa, Ana Berta, Neves, Mariana, Larson, Anna, Quinodoz, Mathieu, Michaelides, Michel, Ben-Yosef, Tamar, Pierce, Eric A., Rivolta, Carlo, Webster, Andrew R., Arno, Gavin, Sharon, Dror, Huckfeldt, Rachel M., Bujakowska, Kinga M.
Publicado 2021