Spectral-Domain Optical Coherence Tomography for Macular Edema von Sallum, Juliana F., Prodocimo, Larissa Maria, Novais, Eduardo, Badaró, Emmerson

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Characterization of Retinal Architecture in Spinocerebellar Ataxia Type 3 and Correlation with Disease Severity von Rezende Filho, Flávio Moura, Jurkute, Neringa, Andrade, João Brainer Clares, Marianelli, Bruna Ferraço, Ferraz Sallum, Juliana M., Yu‐Wai‐Man, Patrick, Barsottini, Orlando G., Pedroso, José Luiz

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Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS von Rezende Filho, Flávio Moura, Parkinson, Michael H., Pedroso, José Luiz, Poh, Roy, Faber, Ingrid, Lourenço, Charles Marques, Júnior, Wilson Marques, França Junior, Marcondes Cavalcante, Kok, Fernando, Sallum, Juliana M. Ferraz, Giunti, Paola, Barsottini, Orlando Graziani Póvoas

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Giant annular posttraumatic choroidal rupture von Unonius, Nichard, MD, Araújo, Jodeilson, MD, Farah, Michel E., MD, Ferraz Sallum, Juliana M., MD, Calucci, Daniela, COMT

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Genetic Heterogeneity of Dominant Optic Atrophy, Kjer Type: Identification of a Second Locus on Chromosome 18q12.2-12.3 von Kerrison, John B, Arnould, Veronique J, Ferraz Sallum, Juliana M, Vagefi, M. Reza, Barmada, M. Michael, Li, Yingying, Zhu, Danping, Maumenee, Irene H

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Síndrome de Wolfram: relato de caso von Fontes, Bruno Machado, Chen, Jane, Príncipe, André Hasler, Sallum, Juliana M. Ferraz, Chicani, Carlos Filipe

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Córnea plana congênita: relato de caso e revisão de literatura von Mascaro, Vera L. D. M., Alvarenga, Lênio S., Sallum, Juliana M. Ferraz, Freitas, Denise de

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Síndrome de Wolfram: relato de caso von Fontes, Bruno Machado, Chen, Jane, Príncipe, André Hasler, Sallum, Juliana M. Ferraz, Chicani, Carlos Filipe

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Classificação diagnóstica dos portadores de doenças degenerativas de retina, integrantes dos grupos Retina São Paulo e Retina Vale do Paraíba von Unonius, Nichard, Farah, Michel Eid, Sallum, Juliana M. Ferraz

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Córnea plana congênita: relato de caso e revisão de literatura von Mascaro, Vera L. D. M., Alvarenga, Lênio S., Sallum, Juliana M. Ferraz, Freitas, Denise de

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Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil von de Melo, Mônica Barbosa, Mandal, Anil K, Tavares, Ivan M, Ali, Mohammed Hasnat, Kabra, Meha, de Vasconcellos, José Paulo Cabral, Senthil, Sirisha, Sallum, Juliana M F, Kaur, Inderjeet, Betinjane, Alberto J, Moura, Christiane R, Paula, Jayter S, Costa, Karita A, Sarfarazi, Mansoor, Paolera, Mauricio Della, Finzi, Simone, Ferraz, Victor E F, Costa, Vital P, Belfort, Jr, Rubens, Chakrabarti, Subhabrata

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics von Khan, Mubeen, Cornelis, Stéphanie S., Pozo-Valero, Marta Del, Whelan, Laura, Runhart, Esmee H., Mishra, Ketan, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F., van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian, Dudakova, Lubica, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian, Glavač, Damjan, Gorin, Michael B., Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M., Hoischen, Alexander, Hoyng, Carel B., Hufendiek, Karsten, Jägle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W., Kousal, Bohdan, Lamey, Tina M., MacDonald, Ian M., Matynia, Anna, McLaren, Terri L., Mena, Marcela D., Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika, Pieterse, Marc, Podhajcer, Osvaldo L., Puech, Bernard, Ramesar, Raj, Rüther, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P., Thompson, Jennifer A., Thuillier, Caroline, Tracewska, Anna M., van Zweeden, Martine, Vincent, Andrea L., Zanlonghi, Xavier, Liskova, Petra, Stöhr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa, Weber, Bernhard H. F., Dhaenens, Claire‐Marie, Cremers, Frans P. M.

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Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease von Runhart, Esmee H, Khan, Mubeen, Cornelis, Stéphanie S, Roosing, Susanne, Del Pozo-Valero, Marta, Lamey, Tina M, Liskova, Petra, Roberts, Lisa, Stöhr, Heidi, Klaver, Caroline C. W, Hoyng, Carel B, Cremers, Frans P. M, Dhaenens, Claire-Marie

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A Prospective, Observational, Non-interventional Clinical Study of Participants With Choroideremia: The NIGHT Study von MACLAREN, ROBERT E., LAM, BYRON L., FISCHER, M. DOMINIK, HOLZ, FRANK G., PENNESI, MARK E., BIRCH, DAVID G., SANKILA, EEVA-MARJA, MEUNIER, ISABELLE ANNE, STEPIEN, KIMBERLY E., SALLUM, JULIANA MARIA FERRAZ, LI, JIANG, YOON, DAN, PANDA, SUSHIL, GOW, JAMES A.

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Clinical and Genetic Characterization of RDH12-Retinal Dystrophy in a South American Cohort von Daich Varela, Malena, Moya, Rene, Azevedo Souza Amaral, Rebeca, Schlottmann, Patricio G, Álvarez Mendiara, Alejandro, Francone, Aníbal, Guazi Resende, Rosane, Capalbo, Luciana, Gelvez, Nancy, López, Greizy, Morales-Acevedo, Ana M, Ossa, Rafael H, Arno, Gavin, Michaelides, Michel, Tamayo, Martha L, Ferraz Sallum, Juliana Maria

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Towards uncovering the role of incomplete penetrance in maculopathies through sequencing of 105 disease-associated genes von Hitti-Malin, Rebekkah J, Panneman, Daan M, Corradi, Zelia, Boonen, Erica G. M, Astuti, Galuh, Dhaenens, Claire-Marie, Stoehr, Heidi, Weber, Bernhard H. F, Sharon, Dror, Banin, Eyal, Karali, Marianthi, Banfi, Sandro, Ben-Yosef, Tamar, Glavac, Damjan, Farrar, G. Jane, Ayuso, Carmen, Liskova, Petra, Dudakova, Lubica, Vajter, Marie, Oldak, Monika, Szaflik, Jacek P, Matynia, Anna, Gorin, Michael B, Kaempjaervi, Kati, Bauwens, Miriam, De Baere, Elfride, Hoyng, Carel B, Li, Catherina H. Z, Klaver, Caroline C. W, Inglehearn, Chris F, Fujinami, Kaoru, Rivolta, Carlo, Allikmets, Rando, Zernant, Jana, Lee, Winston, Podhajcer, Osvaldo L, Fakin, Ana, Sajovic, Jana, Altalbishi, Alaa, Valeina, Sandra, Taurina, Gita, Vincent, Andrea L, Roberts, Lisa, Ramesar, Raj, Sartor, Giovanna, Luppi, Elena, Downes, Susan M, van den Born, L. Ingeborgh, Mclaren, Terri L, De Roach, John N, Lamey, Tina M, Thompson, Jennifer A, Chen, Fred K, Tracewska, Anna M, Kamakari, Smaragda, Sallum, Juliana Maria Ferraz, Bolz, Hanno J, Kayserili, Huelya, Roosing, Susanne, Cremers, Frans P. M

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Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes von Hitti-Malin, Rebekkah J, Panneman, Daan M, Corradi, Zelia, Boonen, Erica G M, Astuti, Galuh, Dhaenens, Claire-Marie, Stöhr, Heidi, Weber, Bernhard H F, Sharon, Dror, Banin, Eyal, Karali, Marianthi, Banfi, Sandro, Ben-Yosef, Tamar, Glavač, Damjan, Farrar, G Jane, Ayuso, Carmen, Liskova, Petra, Dudakova, Lubica, Vajter, Marie, Ołdak, Monika, Szaflik, Jacek P, Matynia, Anna, Gorin, Michael B, Kämpjärvi, Kati, Bauwens, Miriam, De Baere, Elfride, Hoyng, Carel B, Li, Catherina H Z, Klaver, Caroline C W, Inglehearn, Chris F, Fujinami, Kaoru, Rivolta, Carlo, Allikmets, Rando, Zernant, Jana, Lee, Winston, Podhajcer, Osvaldo L, Fakin, Ana, Sajovic, Jana, AlTalbishi, Alaa, Valeina, Sandra, Taurina, Gita, Vincent, Andrea L, Roberts, Lisa, Ramesar, Raj, Sartor, Giovanna, Luppi, Elena, Downes, Susan M, van den Born, L Ingeborgh, McLaren, Terri L, De Roach, John N, Lamey, Tina M, Thompson, Jennifer A, Chen, Fred K, Tracewska, Anna M, Kamakari, Smaragda, Sallum, Juliana Maria Ferraz, Bolz, Hanno J, Kayserili, Hülya, Roosing, Susanne, Cremers, Frans P M

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XOLARIS: A 24-Month, Prospective, Natural History Study of 201 Participants with Retinitis Pigmentosa GTPase Regulator-Associated X-Linked Retinitis Pigmentosa von MacLaren, Robert E., Fischer, M. Dominik, Lam, Byron L., Meunier, Isabelle, Pennesi, Mark E., Sankila, Eeva-Marja K., Gow, James A., Li, Jiang, Tsang, So-Fai, Gregory-Evans, Kevin, Koenekoop, Robert, Sankila, Eeva-Marja K., Riikonen, Antti, Meunier, Isabelle, Fischer, M. Dominik, Stingl, Katarina, Vaheb, Yousof, Richter, Paul, Wozar, Fabian, Reichel, Felix, Gassel, Caroline, Wolfram, Lasse, Fischer, Nora, Peters, Tobias, Wilhelm, Barbara, Seitz, Immanuel, Holz, Frank, Reinking, Katharina, Clemens, Amelie, Völker, Desiree, Herrmann, Philipp, Schipper, Pascal, Weber, Constance, Bulirsch, Louisa, Hoyng, Carel, Klaver, Caroline, Van Huet, Ramon, Boon, Camiel, Nguyen, X.T., Talib, M., Trzcionkowska, Kasia, Tussenbroek, Thomas, MacLaren, Robert E., Taylor, Laura J., Cehajic-Kapetanovic, Jasmina, Josan, Amandeep S., Yusuf, Imran H., Jasani, Kirti, Menghini, Moreno, Nanda, Anika, Rehman, Salwah, Jolly, Jasleen K., Buckley, Thomas M.W., Lotery, Andrew, Thulsidharan, Suresh, Khandhadia, Samir, Tsokolas, Georgios, Black, Graeme, Megaw, Roly, Bishop, Paul, Mukherjee, Rajarshi, Mohla, Aditi, McKibbin, Martin, Mukherjee, Raj, Lam, Byron L., Mendoza-Santiesteban, Carlos, Horowitz, Jason, Tsang, Stephen, Pennesi, Mark E., Yang, Paul, Lauer, Andreas K., Weleber, Richard G., Birch, David, Coors, Lori, Spencer, Rand, Csaky, Karl, Wang, Yi-Zhong, Gorin, Michael, Stepien, Kimberly, Duncan, Jacque L., Stewart, Jay, Moore, Anthony, Stout, J. Timothy, Weng, Christina, Leung, Ella, Schlle, Tahira, Bakall, Benjamin, Klein, Kendra, Bernstein, Paul, Hartnett, Mary Elizabeth, Mathias, Marc, Siringo, Frank, Pecen, Paula, Aleman, Tomas, McGuire, Albert, Nagiel, Aaron, Larsen, Michael, Ferraz Sallum, Juliana Maria, Ribeiro, Lucas, de Azevedo Amaral, Rebeca

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics von Khan, Mubeen, Cornelis, Stephanie S, Del Pozo-Valero, Marta, Whelan, Laura, Runhart, Esmee H, Mishra, Ketan, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F, van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian, Dudakova, Lubica, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian, Glavac, Damjan, Gorin, Michael B, Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M, Hoischen, Alexander, Hoyng, Carel B, Hufendiek, Karsten, Jaegle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W, Kousal, Bohdan, Lamey, Tina M, MacDonald, Ian M, Matynia, Anna, McLaren, Terri L, Mena, Marcela D, Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika, Pieterse, Marc, Podhajcer, Osvaldo L, Puech, Bernard, Ramesar, Raj, Ruether, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P, Thompson, Jennifer A, Thuillier, Caroline, Tracewska, Anna M, van Zweeden, Martine, Vincent, Andrea L, Zanlonghi, Xavier, Liskova, Petra, Stoehr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa, Weber, Bernhard H. F, Dhaenens, Claire-Marie, Cremers, Frans P. M

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Clinical and genetic characterization of RDH12-retinal dystrophy in a South American cohort von Daich Varela, Malena, Moya, Rene, Azevedo Souza Amaral, Rebeca, Schlottmann, Patricio G, Álvarez Mendiara, Alejandro, Francone, Aníbal, Guazi Resende, Rosane, Capalbo, Luciana, Gelvez, Nancy, López, Greizy, Morales-Acevedo, Ana M, Ossa, Rafael H, Arno, Gavin, Michaelides, Michel, Tamayo, Martha L, Ferraz Sallum, Juliana Maria

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