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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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2012 | 1 |
2013 | 2 |
2020 | 1 |
2024 | 0 |
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Functional characterisation of alpha-galactosidase a mutations as a basis for a new classification system in fabry disease.
PLoS Genet. 2013;9(8):e1003632. doi: 10.1371/journal.pgen.1003632. Epub 2013 Aug 1.
PLoS Genet. 2013.
PMID: 23935525
Free PMC article.
Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy.
Terryn W, Deschoenmakere G, De Keyser J, Meersseman W, Van Biesen W, Wuyts B, Hemelsoet D, Pascale H, De Backer J, De Paepe A, Poppe B, Vanholder R.
Terryn W, et al.
Int J Cardiol. 2013 Sep 10;167(6):2555-60. doi: 10.1016/j.ijcard.2012.06.069. Epub 2012 Jul 16.
Int J Cardiol. 2013.
PMID: 22805550
Clinical Trial.
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Correlation between GLA variants and alpha-Galactosidase A profile in dried blood spot: an observational study in Brazilian patients.
Varela P, Mastroianni Kirsztajn G, Motta FL, Martin RP, Turaça LT, Ferrer HLF, Gomes CP, Nicolicht P, Mara Marins M, Pessoa JG, Braga MC, D'Almeida V, Martins AM, Pesquero JB.
Varela P, et al.
Orphanet J Rare Dis. 2020 Jan 29;15(1):30. doi: 10.1186/s13023-019-1274-3.
Orphanet J Rare Dis. 2020.
PMID: 31996269
Free PMC article.
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