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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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Korsholm, Kirsten, Feldt-Rasmussen, Ulla, Granqvist, Henrik, Højgaard, Liselotte, Bollinger, Birgit, Rasmussen, Aase K., Law, Ian
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4667906/
https://ncbi.nlm.nih.gov/pubmed/26629990
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0143940
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