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

Year Number of Results
1923 1
1999 1
2000 1
2001 2
2002 2
2003 2
2004 1
2005 6
2006 2
2007 5
2008 2
2009 5
2010 8
2011 5
2012 19
2013 17
2014 15
2015 15
2016 20
2017 28
2018 25
2019 28
2020 43
2021 34
2022 33
2023 21
2024 0

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Similar articles for PMID: 29330335

285 results

Results by year

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Page 1
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young.
De Brabander I, Yperzeele L, Ceuterick-De Groote C, Brouns R, Baker R, Belachew S, Delbecq J, De Keulenaer G, Dethy S, Eyskens F, Fumal A, Hemelsoet D, Hughes D, Jeangette S, Nuytten D, Redondo P, Sadzot B, Sindic C, Sheorajpanday R, Thijs V, Van Broeckhoven C, De Deyn PP. De Brabander I, et al. Clin Neurol Neurosurg. 2013 Jul;115(7):1088-93. doi: 10.1016/j.clineuro.2012.11.003. Epub 2012 Dec 4. Clin Neurol Neurosurg. 2013. PMID: 23219219
Nationwide screening for Fabry disease in unselected stroke patients.
Tomek A, Petra R, Paulasová Schwabová J, Olšerová A, Škorňa M, Nevšímalová M, Šimůnek L, Herzig R, Fafejtová Š, Mikulenka P, Táboříková A, Neumann J, Brzezny R, Sobolová H, Bartoník J, Václavík D, Vachová M, Bechyně K, Havlíková H, Prax T, Šaňák D, Černíková I, Ondečková I, Procházka P, Rajner J, Škoda M, Novák J, Škoda O, Bar M, Mikulík R, Dostálová G, Linhart A; National Stroke Research Network, part of Czech Clinical Research Infrastructure Network (CZECRIN) and Czech Neurological Society, Cerebrovascular Section. Tomek A, et al. PLoS One. 2021 Dec 14;16(12):e0260601. doi: 10.1371/journal.pone.0260601. eCollection 2021. PLoS One. 2021. PMID: 34905550 Free PMC article.
Use of a rare disease registry for establishing phenotypic classification of previously unassigned GLA variants: a consensus classification system by a multispecialty Fabry disease genotype-phenotype workgroup.
Germain DP, Oliveira JP, Bichet DG, Yoo HW, Hopkin RJ, Lemay R, Politei J, Wanner C, Wilcox WR, Warnock DG. Germain DP, et al. J Med Genet. 2020 Aug;57(8):542-551. doi: 10.1136/jmedgenet-2019-106467. Epub 2020 Mar 11. J Med Genet. 2020. PMID: 32161151 Free PMC article.
Mutations of the GLA gene in young patients with stroke: the PORTYSTROKE study--screening genetic conditions in Portuguese young stroke patients.
Baptista MV, Ferreira S, Pinho-E-Melo T, Carvalho M, Cruz VT, Carmona C, Silva FA, Tuna A, Rodrigues M, Ferreira C, Pinto AA, Leitão A, Gabriel JP, Calado S, Oliveira JP, Ferro JM; PORTuguese Young STROKE Investigators. Baptista MV, et al. Stroke. 2010 Mar;41(3):431-6. doi: 10.1161/STROKEAHA.109.570499. Epub 2010 Jan 28. Stroke. 2010. PMID: 20110537 Clinical Trial.
Frequency of Fabry disease in male and female haemodialysis patients in Spain.
Gaspar P, Herrera J, Rodrigues D, Cerezo S, Delgado R, Andrade CF, Forascepi R, Macias J, del Pino MD, Prados MD, de Alegria PR, Torres G, Vidau P, Sá-Miranda MC. Gaspar P, et al. BMC Med Genet. 2010 Feb 1;11:19. doi: 10.1186/1471-2350-11-19. BMC Med Genet. 2010. PMID: 20122163 Free PMC article.
285 results