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

Year Number of Results
1994 1
1999 7
2000 3
2001 2
2002 3
2003 1
2004 2
2005 3
2006 2
2008 2
2010 1
2013 4
2014 2
2018 1
2022 0
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32 results
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Page 1
[Hereditary macular dystrophies].
Rozet JM, Gerber S, Ducroq D, Hamel C, Dufier JL, Kaplan J. Rozet JM, et al. Among authors: ducroq d. J Fr Ophtalmol. 2005 Jan;28(1):113-24. doi: 10.1016/s0181-5512(05)81033-2. J Fr Ophtalmol. 2005. PMID: 15767907 Review. French.
Leber congenital amaurosis.
Perrault I, Rozet JM, Gerber S, Ghazi I, Leowski C, Ducroq D, Souied E, Dufier JL, Munnich A, Kaplan J. Perrault I, et al. Among authors: ducroq d. Mol Genet Metab. 1999 Oct;68(2):200-8. doi: 10.1006/mgme.1999.2906. Mol Genet Metab. 1999. PMID: 10527670 Review.
A third locus for dominant optic atrophy on chromosome 22q.
Barbet F, Hakiki S, Orssaud C, Gerber S, Perrault I, Hanein S, Ducroq D, Dufier JL, Munnich A, Kaplan J, Rozet JM. Barbet F, et al. Among authors: ducroq d. J Med Genet. 2005 Jan;42(1):e1. doi: 10.1136/jmg.2004.025502. J Med Genet. 2005. PMID: 15635063 Free PMC article. No abstract available.
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis.
Perrault I, Hanein S, Gerber S, Barbet F, Ducroq D, Dollfus H, Hamel C, Dufier JL, Munnich A, Kaplan J, Rozet JM. Perrault I, et al. Among authors: ducroq d. Am J Hum Genet. 2004 Oct;75(4):639-46. doi: 10.1086/424889. Epub 2004 Aug 20. Am J Hum Genet. 2004. PMID: 15322982 Free PMC article.
32 results