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

Year Number of Results
2003 1
2004 2
2005 3
2006 3
2007 3
2008 5
2009 2
2010 3
2011 3
2012 3
2013 3
2014 2
2015 1
2016 3
2017 1
2018 2
2021 3
2022 1
2023 3
2024 3

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Page 1
Artificial intelligence extension of the OSCAR-IB criteria.
Petzold A, Albrecht P, Balcer L, Bekkers E, Brandt AU, Calabresi PA, Deborah OG, Graves JS, Green A, Keane PA, Nij Bijvank JA, Sander JW, Paul F, Saidha S, Villoslada P, Wagner SK, Yeh EA; IMSVISUAL, ERN-EYE Consortium. Petzold A, et al. Ann Clin Transl Neurol. 2021 Jul;8(7):1528-1542. doi: 10.1002/acn3.51320. Epub 2021 May 19. Ann Clin Transl Neurol. 2021. PMID: 34008926 Free PMC article. Review.
MCAT Mutations Cause Nuclear LHON-like Optic Neuropathy.
Gerber S, Orssaud C, Kaplan J, Johansson C, Rozet JM. Gerber S, et al. Among authors: orssaud c. Genes (Basel). 2021 Apr 2;12(4):521. doi: 10.3390/genes12040521. Genes (Basel). 2021. PMID: 33918393 Free PMC article.
Persisting reversed clock syndrome.
Orssaud C, Halimi P, Le Jeunne C, Dufier JL. Orssaud C, et al. Behav Neurol. 2005;16(4):233-6. doi: 10.1155/2005/463428. Behav Neurol. 2005. PMID: 16518014 Free PMC article.
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations.
Perrault I, Saunier S, Hanein S, Filhol E, Bizet AA, Collins F, Salih MA, Gerber S, Delphin N, Bigot K, Orssaud C, Silva E, Baudouin V, Oud MM, Shannon N, Le Merrer M, Roche O, Pietrement C, Goumid J, Baumann C, Bole-Feysot C, Nitschke P, Zahrate M, Beales P, Arts HH, Munnich A, Kaplan J, Antignac C, Cormier-Daire V, Rozet JM. Perrault I, et al. Among authors: orssaud c. Am J Hum Genet. 2012 May 4;90(5):864-70. doi: 10.1016/j.ajhg.2012.03.006. Epub 2012 Apr 12. Am J Hum Genet. 2012. PMID: 22503633 Free PMC article.
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy.
Leruez S, Verny C, Bonneau D, Procaccio V, Lenaers G, Amati-Bonneau P, Reynier P, Scherer C, Prundean A, Orssaud C, Zanlonghi X, Rougier MB, Tilikete C, Miléa D. Leruez S, et al. Among authors: orssaud c. Orphanet J Rare Dis. 2018 Feb 17;13(1):33. doi: 10.1186/s13023-018-0773-y. Orphanet J Rare Dis. 2018. PMID: 29454364 Free PMC article. Clinical Trial.
44 results