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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 3
1995 2
1996 1
1997 4
1999 3
2000 2
2001 9
2002 3
2003 1
2004 1
2005 5
2006 6
2007 2
2008 1
2009 2
2010 4
2011 3
2014 1
2015 2
2019 2
2024 0

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52 results

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Page 1
[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.
[Different indications of photodynamic therapy in ophthalmology].
Lang GE, Mennel S, Spital G, Wachtlin J, Jurklies B, Heimann H, Damato B, Meyer CH. Lang GE, et al. Among authors: jurklies b. Klin Monbl Augenheilkd. 2009 Sep;226(9):725-39. doi: 10.1055/s-0028-1109514. Epub 2009 Jul 14. Klin Monbl Augenheilkd. 2009. PMID: 19603375 Review. German.
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene.
Felden J, Baumann B, Ali M, Audo I, Ayuso C, Bocquet B, Casteels I, Garcia-Sandoval B, Jacobson SG, Jurklies B, Kellner U, Kessel L, Lorenz B, McKibbin M, Meunier I, de Ravel T, Rosenberg T, Rüther K, Vadala M, Wissinger B, Stingl K, Kohl S. Felden J, et al. Among authors: jurklies b. Hum Mutat. 2019 Aug;40(8):1145-1155. doi: 10.1002/humu.23768. Epub 2019 May 6. Hum Mutat. 2019. PMID: 31058429
Angiotensin II in the rabbit retina.
Kohler K, Wheeler-Schilling T, Jurklies B, Guenther E, Zrenner E. Kohler K, et al. Among authors: jurklies b. Vis Neurosci. 1997 Jan-Feb;14(1):63-71. doi: 10.1017/s0952523800008762. Vis Neurosci. 1997. PMID: 9057269
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.
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.
Zeitz C, Michiels C, Neuillé M, Friedburg C, Condroyer C, Boyard F, Antonio A, Bouzidi N, Milicevic D, Veaux R, Tourville A, Zoumba A, Seneina I, Foussard M, Andrieu C, N Preising M, Blanchard S, Saraiva JP, Mesrob L, Le Floch E, Jubin C, Meyer V, Blanché H, Boland A, Deleuze JF, Sharon D, Drumare I, Defoort-Dhellemmes S, De Baere E, Leroy BP, Zanlonghi X, Casteels I, de Ravel TJ, Balikova I, Koenekoop RK, Laffargue F, McLean R, Gottlob I, Bonneau D, Schorderet DF, L Munier F, McKibbin M, Prescott K, Pelletier V, Dollfus H, Perdomo-Trujillo Y, Faure C, Reiff C, Wissinger B, Meunier I, Kohl S, Banin E, Zrenner E, Jurklies B, Lorenz B, Sahel JA, Audo I. Zeitz C, et al. Among authors: jurklies b. Hum Mutat. 2019 Jun;40(6):765-787. doi: 10.1002/humu.23735. Epub 2019 Mar 28. Hum Mutat. 2019. PMID: 30825406
52 results