Comorbidity in patients with branch retinal vein occlusion: case-control study

por Bertelsen, Mette, Linneberg, Allan, Rosenberg, Thomas, Christoffersen, Nynne, Vorum, Henrik, Gade, Else, Larsen, Michael
Publicado 2012

Xeroderma Pigmentosum-Trichothiodystrophy overlap patient with novel XPD/ERCC2 mutation

por Kralund, Henrik H., Ousager, Lilian, Jaspers, Nicolaas G., Raams, Anja, Pedersen, Erling B., Gade, Else, Bygum, Anette
Publicado 2013

Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness

por Davidson, Alice E., Cheong, Sek-Shir, Hysi, Pirro G., Venturini, Cristina, Plagnol, Vincent, Ruddle, Jonathan B., Ali, Hala, Carnt, Nicole, Gardner, Jessica C., Hassan, Hala, Gade, Else, Kearns, Lisa, Jelsig, Anne Marie, Restori, Marie, Webb, Tom R., Laws, David, Cosgrove, Michael, Hertz, Jens M., Russell-Eggitt, Isabelle, Pilz, Daniela T., Hammond, Christopher J., Tuft, Stephen J., Hardcastle, Alison J.
Publicado 2014