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

Year Number of Results
1997 1
2000 1
2003 1
2005 1
2007 1
2008 2
2009 3
2010 4
2011 2
2012 3
2013 4
2014 1
2016 1
2017 2
2018 3
2019 1
2020 1
2021 1
2024 0

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28 results

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Page 1
Retinal hyperreflective foci in Fabry disease.
Atiskova Y, Rassuli R, Koehn AF, Golsari A, Wagenfeld L, du Moulin M, Muschol N, Dulz S. Atiskova Y, et al. Among authors: du moulin m. Orphanet J Rare Dis. 2019 Dec 26;14(1):296. doi: 10.1186/s13023-019-1267-2. Orphanet J Rare Dis. 2019. PMID: 31878969 Free PMC article.
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism.
Coelho D, Kim JC, Miousse IR, Fung S, du Moulin M, Buers I, Suormala T, Burda P, Frapolli M, Stucki M, Nürnberg P, Thiele H, Robenek H, Höhne W, Longo N, Pasquali M, Mengel E, Watkins D, Shoubridge EA, Majewski J, Rosenblatt DS, Fowler B, Rutsch F, Baumgartner MR. Coelho D, et al. Among authors: du moulin m. Nat Genet. 2012 Oct;44(10):1152-5. doi: 10.1038/ng.2386. Epub 2012 Aug 26. Nat Genet. 2012. PMID: 22922874 Free article.
28 results