RECUPERACAO DE INFORMACAO PARAMICROPROCESSADORES.

Por SILVA Eduardo D., Rodrigues, Guilherme Chagas.
Publicado em S197

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 em 2013

Continuing Professional Development: Best Practices

Por Filipe, Helena P., Silva, Eduardo D., Stulting, Andries A., Golnik, Karl C.
Publicado em 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 no PLoS One (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 no Sci Rep (2016)

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 em 2014

Developmental Basis of Nanophthalmos: MFRP is Required for both Prenatal Ocular Growth and Postnatal Emmetropization

Por Sundin, Olof H., Dharmaraj, Sharola, Bhutto, Imran A., Hasegawa, Takuya, McLeod, D. Scott, Merges, Carol A., Silva, Eduardo D., Maumenee, Irene H., Lutty, Gerard A.
Publicado em 2008

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

Por Prasov, Lev, Masud, Tehmina, Khaliq, Shagufta, Mehdi, S. Qasim, Abid, Aiysha, Oliver, Edward R., Silva, Eduardo D., Lewanda, Amy, Brodsky, Michael C., Borchert, Mark, Kelberman, Daniel, Sowden, Jane C., Dattani, Mehul T., Glaser, Tom
Publicado em 2012

Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein

Por Sundin, Olof H., Leppert, Gregory S., Silva, Eduardo D., Yang, Jun-Ming, Dharmaraj, Sharola, Maumenee, Irene H., Santos, Luisa Coutinho, Parsa, Cameron F., Traboulsi, Elias I., Broman, Karl W., DiBernardo, Cathy, Sunness, Janet S., Toy, Jeffrey, Weinberg, Ethan M.
Publicado em 2005

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 no PLoS One (2016)