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

Year Number of Results
1983 1
1991 1
1999 2
2000 1
2001 2
2002 4
2003 4
2004 5
2005 12
2006 10
2007 9
2008 2
2009 8
2010 7
2011 6
2012 9
2013 11
2014 9
2015 19
2016 13
2017 20
2018 19
2019 13
2020 18
2021 17
2022 2
2024 1

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PubMed (Bookshelf cited) for id: 8083

189 results

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Page 1
A review and recommendations for oral chaperone therapy in adult patients with Fabry disease.
Nowicki M, Bazan-Socha S, Błażejewska-Hyżorek B, Kłopotowski MM, Komar M, Kusztal MA, Liberek T, Małyszko J, Mizia-Stec K, Oko-Sarnowska Z, Pawlaczyk K, Podolec P, Sławek J; Polish Fabry Disease Collaborative Group. Nowicki M, et al. Orphanet J Rare Dis. 2024 Jan 18;19(1):16. doi: 10.1186/s13023-024-03028-w. Orphanet J Rare Dis. 2024. PMID: 38238782 Free PMC article. Review.
Fabry Cardiomyopathy: Current Treatment and Future Options.
Vardarli I, Weber M, Rischpler C, Führer D, Herrmann K, Weidemann F. Vardarli I, et al. J Clin Med. 2021 Jul 7;10(14):3026. doi: 10.3390/jcm10143026. J Clin Med. 2021. PMID: 34300196 Free PMC article. Review.
Fabry Disease and the Heart: A Comprehensive Review.
Azevedo O, Cordeiro F, Gago MF, Miltenberger-Miltenyi G, Ferreira C, Sousa N, Cunha D. Azevedo O, et al. Int J Mol Sci. 2021 Apr 23;22(9):4434. doi: 10.3390/ijms22094434. Int J Mol Sci. 2021. PMID: 33922740 Free PMC article. Review.
The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.
Germain DP, Moiseev S, Suárez-Obando F, Al Ismaili F, Al Khawaja H, Altarescu G, Barreto FC, Haddoum F, Hadipour F, Maksimova I, Kramis M, Nampoothiri S, Nguyen KN, Niu DM, Politei J, Ro LS, Vu Chi D, Chen N, Kutsev S. Germain DP, et al. Mol Genet Genomic Med. 2021 May;9(5):e1666. doi: 10.1002/mgg3.1666. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33835733 Free PMC article. Review.
189 results