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

Year Number of Results
1931 1
1990 1
1991 1
1993 1
1998 1
2000 2
2001 1
2003 2
2006 3
2007 1
2008 2
2009 2
2010 4
2011 12
2012 13
2013 6
2014 8
2015 8
2016 12
2017 10
2018 7
2019 2
2020 7
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Similar Articles for PMID: 30300315

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Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.
Meunier I, Manes G, Bocquet B, Marquette V, Baudoin C, Puech B, Defoort-Dhellemmes S, Audo I, Verdet R, Arndt C, Zanlonghi X, Le Meur G, Dhaenens CM, Hamel CP. Meunier I, et al. Ophthalmology. 2014 Dec;121(12):2406-14. doi: 10.1016/j.ophtha.2014.06.028. Epub 2014 Jul 29. Ophthalmology. 2014. PMID: 25085631
Adult-onset foveomacular vitelliform dystrophy: A fresh perspective.
Chowers I, Tiosano L, Audo I, Grunin M, Boon CJ. Chowers I, et al. Prog Retin Eye Res. 2015 Jul;47:64-85. doi: 10.1016/j.preteyeres.2015.02.001. Epub 2015 Feb 11. Prog Retin Eye Res. 2015. PMID: 25681578 Review.
Best Vitelliform Macular Dystrophy.
MacDonald IM, Lee T. MacDonald IM, et al. 2003 Sep 30 [updated 2013 Dec 12]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301346 Free Books & Documents. Review.
Mutations in IMPG1 cause vitelliform macular dystrophies.
Manes G, Meunier I, Avila-Fernández A, Banfi S, Le Meur G, Zanlonghi X, Corton M, Simonelli F, Brabet P, Labesse G, Audo I, Mohand-Said S, Zeitz C, Sahel JA, Weber M, Dollfus H, Dhaenens CM, Allorge D, De Baere E, Koenekoop RK, Kohl S, Cremers FP, Hollyfield JG, Sénéchal A, Hebrard M, Bocquet B, Ayuso García C, Hamel CP. Manes G, et al. Am J Hum Genet. 2013 Sep 5;93(3):571-8. doi: 10.1016/j.ajhg.2013.07.018. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993198 Free PMC article.
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