Neurological manifestations in Fabry's disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/ncpneuro0407.pdf
Reference114 articles.
1. Desnick RJ et al. (1995) Fabry disease: alpha-Galactosidase A deficiency. In The Metabolic and Molecular Bases of Inherited Disease, 2741–2784 (Eds Scriver CR et al.) New York: McGraw Hill
2. Meikle PJ et al. (1999) Prevalence of lysosomal storage disorders. JAMA 281: 249–254
3. Spada M et al. (2006) High incidence of later-onset fabry disease revealed by newborn screening. Am J Hum Genet 79: 31–40
4. Nakao S et al. (2003) Fabry disease: detection of undiagnosed hemodialysis patients and identification of a “renal variant” phenotype. Kidney Int 64: 801–807
5. Rolfs A et al. (2005) Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study. Lancet 366: 1794–1796
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