Multifocal Electroretinograms

Por Creel, Donnell J.
Publicado em 2011

An Inherited Disorder With Splenomegaly, Cytopenias, and Vision Loss

Por Tantravahi, Srinivas K., Williams, Lloyd B., Digre, Kathleen B., Creel, Donnell J., Smock, Kristi J., DeAngelis, Margaret M., Clayton, Frederic C., Vitale, Albert T., Rodgers, George M.
Publicado no Am J Med Genet A (2012)

ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement

Por Xu, Mingchu, Gelowani, Violet, Eblimit, Aiden, Wang, Feng, Young, Marielle P., Sawyer, Briana L., Zhao, Li, Jenkins, Glen, Creel, Donnell J., Wang, Keqing, Ge, Zhongqi, Wang, Hui, Li, Yumei, Hartnett, M. Elizabeth, Chen, Rui
Publicado no Invest Ophthalmol Vis Sci (2015)

EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy

Por Byrne, Susan, Jansen, Lara, U-King-Im, Jean-Marie, Siddiqui, Ata, Lidov, Hart G. W., Bodi, Istvan, Smith, Luke, Mein, Rachael, Cullup, Thomas, Dionisi-Vici, Carlo, Al-Gazali, Lihadh, Al-Owain, Mohammed, Bruwer, Zandre, Al Thihli, Khalid, El-Garhy, Rana, Flanigan, Kevin M., Manickam, Kandamurugu, Zmuda, Erik, Banks, Wesley, Gershoni-Baruch, Ruth, Mandel, Hanna, Dagan, Efrat, Raas-Rothschild, Annick, Barash, Hila, Filloux, Francis, Creel, Donnell, Harris, Michael, Hamosh, Ada, Kölker, Stefan, Ebrahimi-Fakhari, Darius, Hoffmann, Georg F., Manchester, David, Boyer, Philip J., Manzur, Adnan Y., Lourenco, Charles Marques, Pilz, Daniela T., Kamath, Arveen, Prabhakar, Prab, Rao, Vamshi K., Rogers, R. Curtis, Ryan, Monique M., Brown, Natasha J., McLean, Catriona A., Said, Edith, Schara, Ulrike, Stein, Anja, Sewry, Caroline, Travan, Laura, Wijburg, Frits A., Zenker, Martin, Mohammed, Shehla, Fanto, Manolis, Gautel, Mathias, Jungbluth, Heinz
Publicado no Brain (2016)