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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. Among authors: fumal a. 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
Belgian Fabry study: prevalence of Fabry disease in a cohort of 1000 young patients with cerebrovascular disease.
Brouns R, Thijs V, Eyskens F, Van den Broeck M, Belachew S, Van Broeckhoven C, Redondo P, Hemelsoet D, Fumal A, Jeangette S, Verslegers W, Baker R, Hughes D, De Deyn PP; BeFaS Investigators. Brouns R, et al. Among authors: fumal a. Stroke. 2010 May;41(5):863-8. doi: 10.1161/STROKEAHA.110.579409. Epub 2010 Apr 1. Stroke. 2010. PMID: 20360539 Free article.
[Neuroborreliosis].
Machurot PY, Fumal A, Sadzot B. Machurot PY, et al. Among authors: fumal a. Rev Med Liege. 2001 Jan;56(1):11-6. Rev Med Liege. 2001. PMID: 11256131 Review. French.
[Medication overuse headache].
Fumal A, Magis D, Schoenen J. Fumal A, et al. Rev Med Liege. 2006 Apr;61(4):217-22. Rev Med Liege. 2006. PMID: 16789606 Free article. Review. French.
45 results