Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Gade, Else"'
Autor:
Bertelsen, Mette, Linneberg, Allan, Christoffersen, Nynne, Vorum, Henrik, Gade, Else, Larsen, Michael
Publikováno v:
In Ophthalmology March 2014 121(3):637-642
Akademický článek
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Autor:
Bertelsen, Mette, Linneberg, Allan, Rosenberg, Thomas, Christoffersen, Nynne, Vorum, Henrik, Gade, Else, Larsen, Michael
Publikováno v:
BMJ: British Medical Journal, 2012 Dec . 345(7887), 17-17.
Externí odkaz:
https://www.jstor.org/stable/23493303
Publikováno v:
In Ophthalmology 2007 114(6):1186-1189
Akademický článek
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Autor:
Fagerberg, Christina R, Taylor, Adrian, Distelmaier, Felix, Schrøder, Henrik D, Kibæk, Maria, Wieczorek, Dagmar, Tarnopolsky, Mark, Brady, Lauren, Larsen, Martin J, Jamra, Rami A, Seibt, Annette, Hejbøl, Eva Kildall, Gade, Else, Markovic, Ljubo, Klee, Dirk, Nagy, Peter, Rouse, Nicholas, Agarwal, Prasoon, Dolinsky, Vernon W, Bakovic, Marica
Publikováno v:
Brain: A Journal of Neurology; Jan2020, Vol. 143 Issue 1, p94-111, 18p
Autor:
Madsen, Mads Brok Molbech, Gade, Else
Publikováno v:
Madsen, M B M & Gade, E 2016, ' God social funktion hos et barn med kraftig synsnedsættelse på grund af korioretinale kolobomer ', Ugeskrift for Laeger, bind 178, nr. 6, V10150805, s. 534-535 .
A child born with bilateral colobomas was referred to the department of ophthalmology. At birth the child was assumed to be blind. During the follow-up period of seven years his visual acuity improved to 0.08 and he became a socially and intellectual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::ff9ca755b44f458a34e9c959ec329cac
https://portal.findresearcher.sdu.dk/da/publications/e1f76290-90b1-4116-8dfa-01b4c7844eec
https://portal.findresearcher.sdu.dk/da/publications/e1f76290-90b1-4116-8dfa-01b4c7844eec
Autor:
Fagerberg, Christina R, Taylor, Adrian, Distelmaier, Felix, Schrøder, Henrik D, Kibæk, Maria, Wieczorek, Dagmar, Tarnopolsky, Mark, Brady, Lauren, Larsen, Martin J, Jamra, Rami A, Seibt, Annette, Hejbøl, Eva Kildall, Gade, Else, Markovic, Ljubo, Klee, Dirk, Nagy, Peter, Rouse, Nicholas, Agarwal, Prasoon, Dolinsky, Vernon W, Bakovic, Marica
Publikováno v:
Brain: A Journal of Neurology; Jan2019, Vol. 142 Issue 1, p94-111, 18p
Autor:
Andersen, Maria Rene, Gade, Else
Publikováno v:
Andersen, M R & Gade, E 2014, ' Udvikling af opticusneuropati efter beskedent øjetraume ', Ugeskrift for Laeger, bind 176, nr. 3A, V05130330, s. 2-3 .
Traumatic optic neuropathy (TON) is a rare and potentially vision-threatening condition caused by ocular or head trauma. The treatment of TON is controversial with no evidence-based guidelines. We describe a case of an eight-year-old boy, who lost hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::985a04bf346f3641fcdab504d8392998
https://portal.findresearcher.sdu.dk/da/publications/08e1fca6-c491-443c-9198-36bdd0034cb5
https://portal.findresearcher.sdu.dk/da/publications/08e1fca6-c491-443c-9198-36bdd0034cb5
Autor:
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
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104163 (2014)
PLoS ONE
Davidson, A E, Cheong, S-S, Hysi, P G, Venturini, C, Plagnol, V, Ruddle, J B, Ali, H, Carnt, N, Gardner, J C, Hassan, H, Gade, E, Kearns, L, Jelsig, A M, Restori, M, Webb, T R, Laws, D, Cosgrove, M, Hertz, J M, Russell-Eggitt, I, Pilz, D T, Hammond, C J, Tuft, S J & Hardcastle, A J 2014, ' Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness ', PLOS ONE, vol. 9, no. 8, e104163 . https://doi.org/10.1371/journal.pone.0104163
PLoS ONE
Davidson, A E, Cheong, S-S, Hysi, P G, Venturini, C, Plagnol, V, Ruddle, J B, Ali, H, Carnt, N, Gardner, J C, Hassan, H, Gade, E, Kearns, L, Jelsig, A M, Restori, M, Webb, T R, Laws, D, Cosgrove, M, Hertz, J M, Russell-Eggitt, I, Pilz, D T, Hammond, C J, Tuft, S J & Hardcastle, A J 2014, ' Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness ', PLOS ONE, vol. 9, no. 8, e104163 . https://doi.org/10.1371/journal.pone.0104163
We describe novel CHRDL1 mutations in ten families with X-linked megalocornea (MGC1). Our mutation-positive cohort enabled us to establish ultrasonography as a reliable clinical diagnostic tool to distinguish between MGC1 and primary congenital glauc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0caec273642a0b4e592a6838276a00bd
http://europepmc.org/articles/PMC4122416?pdf=render
http://europepmc.org/articles/PMC4122416?pdf=render