{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T13:56:38Z","timestamp":1781704598031,"version":"3.54.5"},"reference-count":12,"publisher":"Norwegian Medical Association","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Tidsskr Nor Legeforen","Tidsskriftet"],"DOI":"10.4045\/tidsskr.17.0802","type":"journal-article","created":{"date-parts":[[2018,8,22]],"date-time":"2018-08-22T09:49:22Z","timestamp":1534931362000},"source":"Crossref","is-referenced-by-count":0,"title":["En ten\u00e5ring med akutt bilateralt synstap"],"prefix":"10.4045","volume":"138","author":[{"given":"Eva Meling","family":"\u00d8degaard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1259-0653","authenticated-orcid":false,"given":"\u00d8ystein Kalsnes","family":"J\u00f8rstad","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emilia","family":"Kerty","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"2479","published-online":{"date-parts":[[2018,8,10]]},"reference":[{"key":"ref=1","doi-asserted-by":"crossref","unstructured":"J\u00f8rstad\u00a0\u00d8K, \u00d8degaard\u00a0EM, Heimdal\u00a0KR et al. Leber hereditary optic neuropathy caused by a mitochondrial DNA 10663T>C point mutation and its response to idebenone treatment. J Neuroophthalmol 2018; 38: 129\u201331. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=29210930&dopt=Abstract","DOI":"10.1097\/WNO.0000000000000598"},{"key":"ref=2","doi-asserted-by":"crossref","unstructured":"Hoorbakht\u00a0H, Bagherkashi\u00a0F. Optic neuritis, its differential diagnosis and management. Open Ophthalmol J 2012; 6: 65\u201372. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=22888383&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.2174%2F1874364101206010065","DOI":"10.2174\/1874364101206010065"},{"key":"ref=3","doi-asserted-by":"crossref","unstructured":"Vaphiades MS, Kline LB. Optic neuritis. I: Kline LB, Foroozan R, red. Optic nerve disorders. Second edition. Oxford: Oxford University Press, 2007: 65\u201384.","DOI":"10.1093\/oso\/9780195312812.003.0004"},{"key":"ref=4","doi-asserted-by":"crossref","unstructured":"Klopstock\u00a0T, Yu-Wai-Man\u00a0P, Dimitriadis\u00a0K et al. A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy. Brain 2011; 134: 2677\u201386. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=21788663&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1093%2Fbrain%2Fawr170","DOI":"10.1093\/brain\/awr170"},{"key":"ref=5","doi-asserted-by":"crossref","unstructured":"Brown\u00a0MD, Starikovskaya\u00a0E, Derbeneva\u00a0O et al. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J. Hum Genet 2002; 110: 130\u20138. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11935318&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1007%2Fs00439-001-0660-8","DOI":"10.1007\/s00439-001-0660-8"},{"key":"ref=6","doi-asserted-by":"crossref","unstructured":"Al-Enezi\u00a0M, Al-Saleh\u00a0H, Nasser\u00a0M. Mitochondrial disorders with significant ophthalmic manifestations. Middle East Afr J Ophthalmol 2008; 15: 81\u20136. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=21346843&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.4103%2F0974-9233.51998","DOI":"10.4103\/0974-9233.51998"},{"key":"ref=7","unstructured":"Wilhelm\u00a0H, Schabet\u00a0M. The diagnosis and treatment of optic neuritis. Dtsch Arztebl Int 2015; 112: 616\u201325, quiz 626. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=26396053&dopt=Abstract"},{"key":"ref=8","unstructured":"Newman\u00a0NJ. Hereditary optic neuropathies: from the mitochondria to the optic nerve. Am J Ophthalmol 2005; 140: 517\u201323. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16083845&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1016%2Fj.ajo.2005.03.017"},{"key":"ref=9","doi-asserted-by":"crossref","unstructured":"Moura\u00a0AL, Nagy\u00a0BV, La Morgia\u00a0C et al. The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cells. Invest Ophthalmol Vis Sci 2013; 54: 4471\u20137. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=23737476&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1167%2Fiovs.12-11137","DOI":"10.1167\/iovs.12-11137"},{"key":"ref=10","doi-asserted-by":"crossref","unstructured":"Yu-Wai-Man\u00a0P, Griffiths\u00a0PG, Hudson\u00a0G et al. Inherited mitochondrial optic neuropathies. J Med Genet 2009; 46: 145\u201358. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=19001017&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1136%2Fjmg.2007.054270","DOI":"10.1136\/jmg.2007.054270"},{"key":"ref=11","doi-asserted-by":"crossref","unstructured":"Sadun\u00a0AA, Carelli\u00a0V, Salomao\u00a0SR et al. Extensive investigation of a large Brazilian pedigree of 11778\/haplogroup J Leber hereditary optic neuropathy. Am J Ophthalmol 2003; 136: 231\u20138. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12888043&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1016%2FS0002-9394(03)00099-0","DOI":"10.1016\/S0002-9394(03)00099-0"},{"key":"ref=12","doi-asserted-by":"crossref","unstructured":"Carelli\u00a0V, Carbonelli\u00a0M, de Coo\u00a0IF et al. International consensus statement on the clinical and therapeutic management of Leber hereditary optic neuropathy. J Neuroophthalmol 2017; 37: 371\u201381. PubMed: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=28991104&dopt=Abstract, Crossref: http:\/\/dx.doi.org\/10.1097%2FWNO.0000000000000570","DOI":"10.1097\/WNO.0000000000000570"}],"container-title":["Tidsskrift for Den norske legeforening"],"original-title":[],"language":"no","deposited":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T13:16:16Z","timestamp":1781702176000},"score":1,"resource":{"primary":{"URL":"https:\/\/tidsskriftet.no\/2018\/08\/noe-laere-av\/en-tenaring-med-akutt-bilateralt-synstap"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,8,10]]},"references-count":12,"journal-issue":{"issue":"12","published-online":{"date-parts":[[2018,8,21]]}},"URL":"https:\/\/doi.org\/10.4045\/tidsskr.17.0802","relation":{},"ISSN":["0029-2001","0807-7096"],"issn-type":[{"value":"0029-2001","type":"print"},{"value":"0807-7096","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,8,10]]}}}