Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey von Mack, Heather G, Chen, Fred K, Grigg, John, Jamieson, Robyn, De Roach, John, O’Hare, Fleur, Britten-Jones, Alexis Ceecee, McGuinness, Myra, Tindill, Nicole, Ayton, Lauren, Cordero, Anai Gonzalez, Edwards, Thomas L, Hewitt, Alex W, Ho, Gladys, Hogden, Michael, Kwan, Anthony, Lamey, Tina, Ma, Alan, Mackey, David, Martin, Keith R, McLaren, Terri, Nash, Benjamin, Ruddle, Jon, Simunovic, Matthew, Sinnerbrink, Ingrid, Taranath, Deepa Ajay, Thompson, Jen, White, Jaclyn

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Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome von Sharan, Sapna, DNB, MNAMS, Swamy, Brighu, MBBS, Taranath, Deepa Ajay, MBBS, MS, Jamieson, Robyn, MBBS, FRACP, Yu, Tao, MD, Wargon, Orli, MBBS, FRACP, Grigg, John R., MBBS, FRACO

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Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders von Jurgens, Julie A., Barry, Brenda J., Chan, Wai-Man, MacKinnon, Sarah, Matos Ruiz, Paola M., England, Eleina M., Pais, Lynn, Groopman, Emily, Russell, Kathryn A., Di Gioia, Silvio Alessandro, Lee, Arthur S., Shaaban, Sherin, Bekele, Sarah, Toffoloni, Melissa, Foster, Emma E., Berube, Lindsay, Rivera-Quiles, Cristina, Mensching, Fiona M., Sanchis-Juan, Alba, Fu, Jack M., Wong, Isaac, Zhao, Xuefang, Wilson, Michael W., Lek, Monkol, Abarca-Barriga, Hugo, Al-Haddad, Christiane, Chacon-Camacho, Oscar Francisco, Chang, Lan, Christiansen, Stephen P., Ciccarelli, Maria Laura, Cordonnier, Monique, Cox, Gerald F., Curry, Cynthia J., Lee Dahm, Thomas, David, Karen L., De Berardinis, Teresa, Demer, Joseph L., Drack, Arlene V., Eggenberger, Eric, Elder, James E., Elliott, Alexandra T., Epley, K. David, Feldman, Hagit Baris, Ferreira, Carlos R., Gerth-Kahlert, Christina, Halliday, Dorothy J., Hanisch, Frank, Hay, Eleanor, Holder, Christopher, Iannaccone, Alessandro, Isenberg, Sherwin J., Kahana, Alon, Kazlas, Melanie, Kerr, Natalie C., Ko, Melissa W., Koc, Feray, Larsen, Dorte Ancher, Lay-Son, Guillermo, Ledoux, Danielle M., Levin, Alex V., Levy, Richard L., Mackey, David A., Mantagos, Iason S., Marti, Candice, Menezes, Manoj P., Mikail, Claudia N., Miller, Kathryn Bisceglia, Miyana, Kaori, Mullineaux, Lisa, Nishimura, Julie K., Noble, A. Gwendolyn, Pavone, Piero, Phalen, James A., Poduri, Annapurna, Polo, Claudia R., Prasov, Lev, Ramos, Feliciano J., Ramos-Caceres, Maria, Robb, Richard M., Rossillion, Béatrice, Smith, Lois E.H., Sorkin, Jeffrey A., Soul, Janet S., Stalker, Heather J., Stasheff, Steven F., Strassberg, Sonya, Thomas, Ioan Talfryn, VanderVeen, Deborah K., Vincent, Andrea L., Wabbels, Bettina, Wong, Agnes M.F., Wu, Carolyn, Yeung, Alison, Young, Terri L., Zwaan, Johan, Brand, Harrison, Talkowski, Michael E., MacArthur, Daniel G., Robson, Caroline D., Engle, Elizabeth C.

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Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series von White, Samuel, Taranath, Ajay, Hanagandi, Prasad, Taranath, Deepa A, To, Minh-Son, Souzeau, Emmanuelle, Siggs, Owen M, Craig, Jamie E

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Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality von Angkasa, Florencia, Mohammadi, Leila, Taranath, Deepa, Taranath, Ajay, Brecht, Marcus

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Aggressive posterior retinopathy of prematurity von Piotto, Lino, Taranath, Ajay, Gent, Roger, Taranath, Deepa

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Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality von Angkasa, Florencia, Mohammadi, Leila, Taranath, Deepa, Taranath, Ajay, Brecht, Marcus

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