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[Multifocal electroretinography (mfERG)].
Seeliger MW, Jurklies B, Kellner U, Palmowski A, Bach M, Kretschmann U. Seeliger MW, et al. Among authors: jurklies b. Ophthalmologe. 2001 Nov;98(11):1112-27; quiz 1128-9. doi: 10.1007/s003470170036. Ophthalmologe. 2001. PMID: 11729748 Review. German. No abstract available.
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, Kellner U, Lorenz B, Salati R, Jurklies B, Farkas A, Andreasson S, Weleber RG, Jacobson SG, Rudolph G, Castellan C, Dollfus H, Legius E, Anastasi M, Bitoun P, Lev D, Sieving PA, Munier FL, Zrenner E, Sharpe LT, Cremers FP, Wissinger B. Kohl S, et al. Among authors: jurklies b. Eur J Hum Genet. 2005 Mar;13(3):302-8. doi: 10.1038/sj.ejhg.5201269. Eur J Hum Genet. 2005. PMID: 15657609
CNGA3 mutations in hereditary cone photoreceptor disorders.
Wissinger B, Gamer D, Jägle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklies B, Rosenberg T, Jacobson SG, Sener EC, Tatlipinar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FP, Apfelstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S. Wissinger B, et al. Among authors: jurklies b. Am J Hum Genet. 2001 Oct;69(4):722-37. doi: 10.1086/323613. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536077 Free PMC article.
EFEMP1 is not associated with sporadic early onset drusen.
Sauer CG, White K, Kellner U, Rudolph G, Jurklies B, Pauleikhoff D, Weber BH. Sauer CG, et al. Among authors: jurklies b. Ophthalmic Genet. 2001 Mar;22(1):27-34. doi: 10.1076/opge.22.1.27.2239. Ophthalmic Genet. 2001. PMID: 11262647
[Comparison of superselective intraarterial fibrinolysis with conservative therapy. Use in patients with acute non-arteritic central retinal artery occlusion].
Wolf A, Schumacher M, Neubauer AS, Schmoor C, Gall C, Jurklies B, Wanke I, Solymosi L, Brückmann H, Schmidt D, Feltgen N; European Assessment Group for Lysis in the Eye Studien Gruppe. Wolf A, et al. Among authors: jurklies b. Ophthalmologe. 2010 Sep;107(9):799-805. doi: 10.1007/s00347-010-2247-z. Ophthalmologe. 2010. PMID: 20821332 Clinical Trial. German.
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.
den Hollander AI, Heckenlively JR, van den Born LI, de Kok YJ, van der Velde-Visser SD, Kellner U, Jurklies B, van Schooneveld MJ, Blankenagel A, Rohrschneider K, Wissinger B, Cruysberg JR, Deutman AF, Brunner HG, Apfelstedt-Sylla E, Hoyng CB, Cremers FP. den Hollander AI, et al. Among authors: jurklies b. Am J Hum Genet. 2001 Jul;69(1):198-203. doi: 10.1086/321263. Epub 2001 May 24. Am J Hum Genet. 2001. PMID: 11389483 Free PMC article.
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