Switching to ranibizumab in diabetic macular oedema refractory to bevacizumab treatment by Ashraf, M, Souka, A A, Daich Varela, M, El Kayal, H, Schlottmann, P G

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Switching to ranibizumab in diabetic macular oedema refractory to bevacizumab treatment by Ashraf, M., Souka, A.A., Daich Varela, M., el Kayal, H., Schlottmann, P.G.

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SynthEye: Investigating the Impact of Synthetic Data on Artificial Intelligence-assisted Gene Diagnosis of Inherited Retinal Disease by Veturi, Yoga Advaith, Woof, William, Lazebnik, Teddy, Moghul, Ismail, Woodward-Court, Peter, Wagner, Siegfried K., Cabral de Guimarães, Thales Antonio, Daich Varela, Malena, Liefers, Bart, Patel, Praveen J., Beck, Stephan, Webster, Andrew R., Mahroo, Omar, Keane, Pearse A., Michaelides, Michel, Balaskas, Konstantinos, Pontikos, Nikolas

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The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature by Varela, Malena Daich, Jani, Priyam, Zein, Wadih M., D'Souza, Precilla, Wolfe, Lynne, Chisholm, Jennifer, Zalewski, Christopher, Adams, David, Warner, Blake M., Huryn, Laryssa A., Hufnagel, Robert B.

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Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies by Daich Varela, Malena, Bellingham, James, Motta, Fabiana, Jurkute, Neringa, Ellingford, Jamie M, Quinodoz, Mathieu, Oprych, Kathryn, Niblock, Michael, Janeschitz-Kriegl, Lucas, Kaminska, Karolina, Cancellieri, Francesca, Scholl, Hendrik P N, Lenassi, Eva, Schiff, Elena, Knight, Hannah, Black, Graeme, Rivolta, Carlo, Cheetham, Michael E, Michaelides, Michel, Mahroo, Omar A, Moore, Anthony T, Webster, Andrew R, Arno, Gavin

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Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene) by Nguyen, Quang, Woof, William, Kabiri, Nathaniel, Sen, Sagnik, Daich Varela, Malena, Cabral De Guimaraes, Thales Antonio, Shah, Mital, Sumodhee, Dayyanah, Moghul, Ismail, Al-Khuzaei, Saoud, Liu, Yichen, Hollyhead, Catherine, Tailor, Bhavna, Lobo, Loy, Veal, Carl, Archer, Stephen, Furman, Jennifer, Arno, Gavin, Gomes, Manuel, Fujinami, Kaoru, Madhusudhan, Savita, Mahroo, Omar A, Webster, Andrew R, Balaskas, Konstantinos, Downes, Susan M, Michaelides, Michel, Pontikos, Nikolas, Hollyhead, Catherine, Tailor, Bhavna, Lobo, Loy, Veal, Carl, Archer, Stephen

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A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis by Schiff, Elena R., Daich Varela, Malena, Robson, Anthony G., Pierpoint, Karen, Ba‐Abbad, Rola, Nutan, Savita, Zein, Wadih M., Ullah, Ehsan, Huryn, Laryssa A., Tuupanen, Sari, Mahroo, Omar A., Michaelides, Michel, Burke, Derek, Harvey, Katie, Arno, Gavin, Hufnagel, Robert B., Webster, Andrew R.

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Ophthalmic genetics in South America by Daich Varela, Malena, Moya, Rene, Schlottmann, Patricio G., Hufnagel, Robert B., Arberas, Claudia, Fernández, Federico M., Inga, M. Eugenia, Lores, Juliana, Pachajoa, Harry, Prada, Carlos E., Sallum, Juliana M. Ferraz

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Multimodal evaluation of osteosarcoma choroidal metastasis by Fernández Mancebo, Federico M., Inga, M. Eugenia, Daich Varela, Malena

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Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina by Schlottmann, Patricio G., Luna, José D., Labat, Natalia, Yadarola, María Belén, Bainttein, Silvina, Esposito, Evangelina, Ibañez, Agustina, Barbaro, Evangelina Ivón, Álvarez Mendiara, Alejandro, Picotti, Carolina P., Chirino Misisian, Andrea, Andreussi, Luciana, Gras, Julieta, Capalbo, Luciana, Visotto, Mauro, Dipierri, José E., Alcoba, Emilio, Fernández Gabrielli, Laura, Ávila, Silvia, Aucar, María Emilia, Martin, Daniel M., Ormaechea, Gerardo Juan, Inga, M. Eugenia, Francone, Aníbal A., Charles, Martin, Zompa, Tamara, Pérez, Pablo Javier, Lotersztein, Vanesa, Nuova, Pedro J., Canonero, Ivana B., Mahroo, Omar A., Michaelides, Michel, Arno, Gavin, Daich Varela, Malena

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Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom by Woof, William A., de Guimarães, Thales A.C., Al-Khuzaei, Saoud, Daich Varela, Malena, Sen, Sagnik, Bagga, Pallavi, Mendes, Bernardo, Shah, Mital, Burke, Paula, Parry, David, Lin, Siying, Naik, Gunjan, Ghoshal, Biraja, Liefers, Bart J., Fu, Dun Jack, Georgiou, Michalis, Nguyen, Quang, Sousa da Silva, Alan, Liu, Yichen, Fujinami-Yokokawa, Yu, Sumodhee, Dayyanah, Patel, Praveen, Furman, Jennifer, Moghul, Ismail, Moosajee, Mariya, Sallum, Juliana, De Silva, Samantha R., Lorenz, Birgit, Holz, Frank G., Fujinami, Kaoru, Webster, Andrew R., Mahroo, Omar A., Downes, Susan M., Madhusudhan, Savita, Balaskas, Konstantinos, Michaelides, Michel, Pontikos, Nikolas

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