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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Korsholm, Kirsten, Feldt-Rasmussen, Ulla, Granqvist, Henrik, Højgaard, Liselotte, Bollinger, Birgit, Rasmussen, Aase K., Law, Ian
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2015
Aiheet:
Research Article
Linkit: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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