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Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness.
Davidson AE, Cheong SS, Hysi PG, Venturini C, Plagnol V, Ruddle JB, Ali H, Carnt N, Gardner JC, Hassan H, Gade E, Kearns L, Jelsig AM, Restori M, Webb TR, Laws D, Cosgrove M, Hertz JM, Russell-Eggitt I, Pilz DT, Hammond CJ, Tuft SJ, Hardcastle AJ. Davidson AE, et al. Among authors: gade e. PLoS One. 2014 Aug 5;9(8):e104163. doi: 10.1371/journal.pone.0104163. eCollection 2014. PLoS One. 2014. PMID: 25093588 Free PMC article.
Mortality in patients with central retinal vein occlusion.
Bertelsen M, Linneberg A, Christoffersen N, Vorum H, Gade E, Larsen M. Bertelsen M, et al. Among authors: gade e. Ophthalmology. 2014 Mar;121(3):637-42. doi: 10.1016/j.ophtha.2013.07.025. Epub 2013 Sep 17. Ophthalmology. 2014. PMID: 24053999
Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration.
Fagerberg CR, Taylor A, Distelmaier F, Schrøder HD, Kibæk M, Wieczorek D, Tarnopolsky M, Brady L, Larsen MJ, Jamra RA, Seibt A, Hejbøl EK, Gade E, Markovic L, Klee D, Nagy P, Rouse N, Agarwal P, Dolinsky VW, Bakovic M. Fagerberg CR, et al. Among authors: gade e. Brain. 2020 Jan 1;143(1):94-111. doi: 10.1093/brain/awz376. Brain. 2020. PMID: 31855247
Mortality in patients with branch retinal vein occlusion.
Christoffersen N, Gade E, Knudsen L, Juel K, Larsen M. Christoffersen N, et al. Among authors: gade e. Ophthalmology. 2007 Jun;114(6):1186-9. doi: 10.1016/j.ophtha.2007.01.031. Ophthalmology. 2007. PMID: 17544777
49 results