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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
2009 | 1 |
2010 | 1 |
2016 | 1 |
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2019 | 1 |
2024 | 0 |
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Baseline characteristics of patients enrolled in the Canadian Fabry Disease Initiative.
Mol Genet Metab. 2010 Apr;99(4):367-73. doi: 10.1016/j.ymgme.2009.11.001. Epub 2009 Nov 16.
Mol Genet Metab. 2010.
PMID: 20022777
Clinical Trial.
Two novel mutations (L32P) and (G85N) among five different missense mutations in six Danish families with Fabry's disease.
Madsen KM, Hasholt L, Sørensen SA, Fermér ML, Dahl N.
Madsen KM, et al.
Hum Mutat. 1995;5(3):277-8. doi: 10.1002/humu.1380050316.
Hum Mutat. 1995.
PMID: 7599642
No abstract available.
Item in Clipboard
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study.
Hughes DA, Nicholls K, Shankar SP, Sunder-Plassmann G, Koeller D, Nedd K, Vockley G, Hamazaki T, Lachmann R, Ohashi T, Olivotto I, Sakai N, Deegan P, Dimmock D, Eyskens F, Germain DP, Goker-Alpan O, Hachulla E, Jovanovic A, Lourenco CM, Narita I, Thomas M, Wilcox WR, Bichet DG, Schiffmann R, Ludington E, Viereck C, Kirk J, Yu J, Johnson F, Boudes P, Benjamin ER, Lockhart DJ, Barlow C, Skuban N, Castelli JP, Barth J, Feldt-Rasmussen U.
Hughes DA, et al.
J Med Genet. 2017 Apr;54(4):288-296. doi: 10.1136/jmedgenet-2016-104178. Epub 2016 Nov 10.
J Med Genet. 2017.
PMID: 27834756
Free PMC article.
Clinical Trial.
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Prevalence of Fabry disease in male dialysis patients: Argentinean screening study.
Frabasil J, Durand C, Sokn S, Gaggioli D, Carozza P, Carabajal R, Politei J, Schenone AB.
Frabasil J, et al.
JIMD Rep. 2019 May 2;48(1):45-52. doi: 10.1002/jmd2.12035. eCollection 2019 Jul.
JIMD Rep. 2019.
PMID: 31392112
Free PMC article.
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