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

Year Number of Results
1997 1
1999 2
2000 1
2002 4
2003 2
2005 1
2007 4
2008 4
2009 1
2010 4
2011 5
2012 11
2013 10
2014 8
2015 6
2016 6
2017 2
2018 9
2019 4
2020 4
2021 3
2022 4
2023 4
2024 0

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84 results

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Page 1
Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study.
Arends M, Biegstraaten M, Wanner C, Sirrs S, Mehta A, Elliott PM, Oder D, Watkinson OT, Bichet DG, Khan A, Iwanochko M, Vaz FM, van Kuilenburg ABP, West ML, Hughes DA, Hollak CEM. Arends M, et al. Among authors: sirrs s. J Med Genet. 2018 May;55(5):351-358. doi: 10.1136/jmedgenet-2017-104863. Epub 2018 Feb 7. J Med Genet. 2018. PMID: 29437868 Free PMC article.
Echocardiographic Assessment of Patients with Fabry Disease.
Yeung DF, Sirrs S, Tsang MYC, Gin K, Luong C, Jue J, Nair P, Lee PK, Tsang TSM. Yeung DF, et al. Among authors: sirrs s. J Am Soc Echocardiogr. 2018 Jun;31(6):639-649.e2. doi: 10.1016/j.echo.2018.01.016. Epub 2018 Mar 29. J Am Soc Echocardiogr. 2018. PMID: 29606333 Review.
Consensus clinical management guidelines for Niemann-Pick disease type C.
Geberhiwot T, Moro A, Dardis A, Ramaswami U, Sirrs S, Marfa MP, Vanier MT, Walterfang M, Bolton S, Dawson C, Héron B, Stampfer M, Imrie J, Hendriksz C, Gissen P, Crushell E, Coll MJ, Nadjar Y, Klünemann H, Mengel E, Hrebicek M, Jones SA, Ory D, Bembi B, Patterson M; International Niemann-Pick Disease Registry (INPDR). Geberhiwot T, et al. Among authors: sirrs s. Orphanet J Rare Dis. 2018 Apr 6;13(1):50. doi: 10.1186/s13023-018-0785-7. Orphanet J Rare Dis. 2018. PMID: 29625568 Free PMC article. Review.
The Genetic Challenges and Opportunities in Advanced Heart Failure.
Hannah-Shmouni F, Seidelmann SB, Sirrs S, Mani A, Jacoby D. Hannah-Shmouni F, et al. Among authors: sirrs s. Can J Cardiol. 2015 Nov;31(11):1338-50. doi: 10.1016/j.cjca.2015.07.735. Epub 2015 Aug 21. Can J Cardiol. 2015. PMID: 26518444 Free PMC article. Review.
84 results