Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalities

por Violante, Inês R, Ribeiro, Maria J, Silva, Eduardo D, Castelo-Branco, Miguel
Publicado 2013

Continuing Professional Development: Best Practices

por Filipe, Helena P., Silva, Eduardo D., Stulting, Andries A., Golnik, Karl C.
Publicado 2014

Cultural Adaptation of the Portuguese Version of the “Sniffin’ Sticks” Smell Test: Reliability, Validity, and Normative Data

por Ribeiro, João Carlos, Simões, João, Silva, Filipe, Silva, Eduardo D., Hummel, Cornelia, Hummel, Thomas, Paiva, António
Publicado 2016

Accelerated age-related olfactory decline among type 1 Usher patients

por Ribeiro, João Carlos, Oliveiros, Bárbara, Pereira, Paulo, António, Natália, Hummel, Thomas, Paiva, António, Silva, Eduardo D.
Publicado 2016

Novel Insights in the Management of Vernal Keratoconjunctivitis (VKC): European Expert Consensus Using a Modified Nominal Group Technique

por Dahlmann-Noor, Annegret, Bonini, Stefano, Bremond-Gignac, Dominique, Heegaard, Steffen, Leonardi, Andrea, Montero, Jesús, Silva, Eduardo D.
Publicado 2023

Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits

por Ribeiro, Maria J, d’Almeida, Otília C, Ramos, Fabiana, Saraiva, Jorge, Silva, Eduardo D, Castelo-Branco, Miguel
Publicado 2014

Amblyopia screening effectiveness at 3–4 years old: a cohort study

por Guimaraes, Sandra, Soares, Andreia, Freitas, Cristina, Barros, Pedro, Leite, Ricardo Dourado, Costa, Patrício Soares, Silva, Eduardo D
Publicado 2021

Brain damage serum biomarkers induced by COVID-19 in patients from northeast Brazil

por Silva, Ryan C., da Rosa, Michelle M., Leão, Heloísa I., Silva, Eduardo D. L., Ferreira, Nathália T., Albuquerque, Amanda P. B., Duarte, Gisele S., Siqueira, André M., Pereira, Michelly C., Rêgo, Moacyr J. B. M., Pitta, Maira G. R.
Publicado 2023

The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene

por Peter, Virginie G., Quinodoz, Mathieu, Pinto-Basto, Jorge, Sousa, Sergio B., Di Gioia, Silvio Alessandro, Soares, Gabriela, Ferraz Leal, Gabriela, Silva, Eduardo D., Pescini Gobert, Rosanna, Miyake, Noriko, Matsumoto, Naomichi, Engle, Elizabeth C., Unger, Sheila, Shapiro, Frederic, Superti-Furga, Andrea, Rivolta, Carlo, Campos-Xavier, Belinda
Publicado 2019

SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma

por Young, Terri L., Whisenhunt, Kristina N., Jin, Jing, LaMartina, Sarah M., Martin, Sean M., Souma, Tomokazu, Limviphuvadh, Vachiranee, Suri, Fatemeh, Souzeau, Emmanuelle, Zhang, Xue, Dan, Yongwook, Anagnos, Evie, Carmona, Susana, Jody, Nicole M., Stangel, Nickie, Higuchi, Emily C., Huang, Samuel J., Siggs, Owen M., Simões, Maria José, Lawson, Brendan M., Martin, Jacob S., Elahi, Elahe, Narooie-Nejad, Mehrnaz, Motlagh, Behzad Fallahi, Quaggin, Susan E., Potter, Heather D., Silva, Eduardo D., Craig, Jamie E., Egas, Conceição, Maroofian, Reza, Maurer-Stroh, Sebastian, Bradfield, Yasmin S., Tompson, Stuart W.
Publicado 2020

Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome

por Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M., Williamson, Kathleen A., Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre, Meire, Francoise, Fantes, Judy, Franco, Brunella, Lorenz, Birgit, Taylor, David S., Stewart, Fiona, Willoughby, Colin E., McEntagart, Meriel, Khaw, Peng Tee, Clericuzio, Carol, Van Maldergem, Lionel, Williams, Denise, Newbury-Ecob, Ruth, Traboulsi, Elias I., Silva, Eduardo D., Madlom, Mukhlis M., Goudie, David R., Fleck, Brian W., Wieczorek, Dagmar, Kohlhase, Juergen, McTrusty, Alice D., Gardiner, Carol, Yale, Christopher, Moore, Anthony T., Russell-Eggitt, Isabelle, Islam, Lily, Lees, Melissa, Beales, Philip L., Tuft, Stephen J., Solano, Juan B., Splitt, Miranda, Hertz, Jens Michael, Prescott, Trine E., Shears, Deborah J., Nischal, Ken K., Doco-Fenzy, Martine, Prieur, Fabienne, Temple, I. Karen, Lachlan, Katherine L., Damante, Giuseppe, Morrison, Danny A., van Heyningen, Veronica, FitzPatrick, David R.
Publicado 2016