Pseudo-Foster Kennedy Syndrome due to unilateral optic nerve hypoplasia: a case report

بواسطة Bansal, Shveta, Dabbs, Timothy, Long, Vernon
منشور في 2008

Paediatric case of peripapillary choroidal neovascularisation associated with optic disc drusen treated with aflibercept

بواسطة Gan, Weh Loong, Long, Vernon W
الحاوية / القاعدة BMJ Case Rep (2019)

A rare cause of upper airway obstruction in neonates

بواسطة Alia, Rana, Jeeva, Irfan, Miall, Lawrence, Long, Vernon
الحاوية / القاعدة BMJ Case Rep (2012)

Exudative retinopathy in a girl with alström syndrome due to a novel mutation

بواسطة Gogi, Devina, Bond, Jackie, Long, Vernon, Sheridan, Eammon, Woods, C G
منشور في 2007

Retinopathy of prematurity in the United Kingdom: retreatment rates, visual and structural 1-year outcomes

بواسطة Adams, Gillian GW, Bunce, Catey, Xing, Wen, Butler, Lucilla, Long, Vernon, Reddy, Aravind, Dahlmann-Noor, Annegret H.
الحاوية / القاعدة Eye (Lond) (2018)

Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at risk

بواسطة Adams, Gillian G W, Bunce, Catey, Xing, Wen, Butler, Lucilla, Long, Vernon, Reddy, Aravind, Dahlmann-Noor, Annegret H
الحاوية / القاعدة BMJ Open (2017)

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

بواسطة Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina
منشور في 2012

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

بواسطة Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina
منشور في 2012