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Results by year

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

Year Number of Results
1979 1
1982 1
1985 2
1986 1
1987 1
1988 1
1989 1
1992 5
1994 3
1997 2
1999 1
2000 2
2001 1
2006 1
2008 1
2009 3
2010 1
2011 3
2012 3
2013 5
2014 2
2015 2
2016 1
2017 1
2018 2
2024 0

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45 results

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Page 1
Correspondence.
Boon CJ, van den Born LI, Keunen JE, Bergen AA, Riemslag FC, Florijn RJ, van Schooneveld MJ. Boon CJ, et al. Among authors: riemslag fc. Retina. 2015 Sep;35(9):e57-8. doi: 10.1097/IAE.0000000000000696. Retina. 2015. PMID: 26312452 No abstract available.
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.
Littink KW, Stappers PTY, Riemslag FCC, Talsma HE, van Genderen MM, Cremers FPM, Collin RWJ, van den Born LI. Littink KW, et al. Among authors: riemslag fcc. Genes (Basel). 2018 Jan 30;9(2):68. doi: 10.3390/genes9020068. Genes (Basel). 2018. PMID: 29385733 Free PMC article.
A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.
Kohl S, Coppieters F, Meire F, Schaich S, Roosing S, Brennenstuhl C, Bolz S, van Genderen MM, Riemslag FC; European Retinal Disease Consortium; Lukowski R, den Hollander AI, Cremers FP, De Baere E, Hoyng CB, Wissinger B. Kohl S, et al. Among authors: riemslag fc. Am J Hum Genet. 2012 Sep 7;91(3):527-32. doi: 10.1016/j.ajhg.2012.07.006. Epub 2012 Aug 16. Am J Hum Genet. 2012. PMID: 22901948 Free PMC article.
The electrooculogram: a refinement of the method.
Riemslag FC, Verduyn Lunel HF, Spekreijse H. Riemslag FC, et al. Doc Ophthalmol. 1989 Dec;73(4):369-75. doi: 10.1007/BF00154492. Doc Ophthalmol. 1989. PMID: 2637119
45 results