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Positron Emission Tomography and Magnetic Resonance Imaging of the Brain in Fabry Disease: A Nationwide, Long-Time, Prospective Follow-Up

BACKGROUND: Fabry disease is a rare metabolic glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme α-galactosidase A—leading to cellular accumulation of globotriasylceramide in different organs, vessels, tissues, and nerves. The disease is associated with an increased risk...

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Detalles Bibliográficos
Autores principales:	Korsholm, Kirsten, Feldt-Rasmussen, Ulla, Granqvist, Henrik, Højgaard, Liselotte, Bollinger, Birgit, Rasmussen, Aase K., Law, Ian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667906/ https://www.ncbi.nlm.nih.gov/pubmed/26629990 http://dx.doi.org/10.1371/journal.pone.0143940

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