Diagnosing Paraproteinemic Keratopathy: A Case Report

por Mok, Eugenie, Kam, Ka Wai, Aldave, Anthony J., Young, Alvin L.
Publicado 2021

Primary graft failure associated with epithelial downgrowth: a case report

por Aldave, Anthony J, Hollander, David A, Branco, Bruno, Crawford, Brooks, Abbott, Richard L
Publicado 2005

Sutured Custom Foldable Silicone Artificial Iris Implantation Combined With Intraocular Lens Implantation and Penetrating Keratoplasty: Safety and Efficacy Outcomes

por Bonnet, Clemence, Vazirnia, Parsia, Deng, Sophie X., Aldave, Anthony J., Miller, Kevin M.
Publicado 2021

Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal d...

por Bakhtiari, Pejman, Frausto, Ricardo F., Roldan, Ashley N., Wang, Cynthia, Yu, Fei, Aldave, Anthony J.
Publicado 2013

Investigating the Molecular Basis of PPCD3: Characterization of ZEB1 Regulation of COL4A3 Expression

por Chung, Duk-Won D., Frausto, Ricardo F., Chiu, Stephan, Lin, Benjamin R., Aldave, Anthony J.
Publicado 2016

Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus

por Le, Derek J., Chung, Duk-Won D., Frausto, Ricardo F., Kim, Michelle J., Aldave, Anthony J.
Publicado 2016

Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy

por Chung, Doug D., Frausto, Ricardo F., Lin, Benjamin R., Hanser, Evelyn M., Cohen, Zack, Aldave, Anthony J.
Publicado 2017

Identification of a novel partial deletion of STS associated with pre-Descemet corneal dystrophy and X-linked ichthyosis

por Williams, Dominic, Onyia, Onyinye, Chung, Doug D., Kirakosyan, Artak, Hovakimyan, Anna, Payne, Carter, Moshirfar, Majid, Aldave, Anthony J.
Publicado 2023

The utility of next-generation sequencing in the evaluation of the posterior polymorphous corneal dystrophy 1 locus

por Lai, Isabella N., Yellore, Vivek S., Rayner, Sylvia A., D’Silva, Nerissa C., Nguyen, Catherine K., Aldave, Anthony J.
Publicado 2010

Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy

por Lin, Benjamin R., Frausto, Ricardo F., Vo, Rosalind C., Chiu, Stephan Y., Chen, Judy L., Aldave, Anthony J.
Publicado 2016

Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12

por Kim, Michelle J., Frausto, Ricardo F., Rosenwasser, George O. D., Bui, Tina, Le, Derek J., Stone, Edwin M., Aldave, Anthony J.
Publicado 2014

Identification of novel PIKFYVE gene mutations associated with Fleck corneal dystrophy

por Gee, Jessica A., Frausto, Ricardo F., Chung, Duk-Won D., Tangmonkongvoragul, Chulaluck, Le, Derek J., Wang, Cynthia, Han, Jonathan, Aldave, Anthony. J.
Publicado 2015

Twelve-Month Clinical and Histopathological Performance of a Novel Synthetic Cornea Device in Rabbit Model

por Akpek, Esen Karamursel, Aldave, Anthony J., Amescua, Guillermo, Colby, Kathryn A., Cortina, Maria S., de la Cruz, Jose, Parel, Jean-Marie A., Li, Gavin
Publicado 2023

Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell function

por Zakharevich, Marina, Kattan, Jaffer M., Chen, Judy L., Lin, Benjamin R., Cervantes, Aleck E., Chung, Doug D., Frausto, Ricardo F., Aldave, Anthony J.
Publicado 2017

Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies

por Zhang, Wenlin, Frausto, Ricardo, Chung, Doug D., Griffis, Christopher G., Kao, Liyo, Chen, Angela, Azimov, Rustam, Sampath, Alapakkam P., Kurtz, Ira, Aldave, Anthony J.
Publicado 2020

Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy

por Chen, Judy L., Lin, Benjamin R., Gee, Katherine M., Gee, Jessica A., Chung, Duk-Won D., Frausto, Ricardo F., Deng, Sophie X., Aldave, Anthony J.
Publicado 2015

Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1

por Chung, Doug D., Frausto, Ricardo F., Cervantes, Aleck E., Gee, Katherine M., Zakharevich, Marina, Hanser, Evelyn M., Stone, Edwin M., Heon, Elise, Aldave, Anthony J.
Publicado 2017

Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously M...

por Lin, Benjamin R., Le, Derek J., Chen, Yabin, Wang, Qiwei, Chung, D. Doug, Frausto, Ricardo F., Croasdale, Christopher, Yee, Richard W., Hejtmancik, Fielding J., Aldave, Anthony J.
Publicado 2016

Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy

por Dong, Pham Ngoc, Cung, Le Xuan, Sam, Tran Khanh, Hang, Do Thi Thuy, Chung, Doug D., Alkadi, Turad A., Buckshey, Arjun, Zhang, Junwei, Kassels, Alexa, Aldave, Anthony J.
Publicado 2020

Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy

por Igo, Robert P., Kopplin, Laura J., Joseph, Peronne, Truitt, Barbara, Fondran, Jeremy, Bardenstein, David, Aldave, Anthony J., Croasdale, Christopher R., Price, Marianne O., Rosenwasser, Miriam, Lass, Jonathan H., Iyengar, Sudha K.
Publicado 2012