Enzyme replacement reverses abnormal cerebrovascular responses in Fabry disease

BACKGROUND: Fabry disease is a lysosomal X-linked enzyme deficiency of α-galactosidase A associated with an increased mortality and morbidity due to renal failure, cardiac disease and early onset stroke. METHODS: We examined the functional blood flow response of the brain after visual stimulation (r...

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Detalles Bibliográficos
Autores principales: Moore, David F, Altarescu, Gheona, Herscovitch, Peter, Schiffmann, Raphael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC116601/
https://www.ncbi.nlm.nih.gov/pubmed/12079501
http://dx.doi.org/10.1186/1471-2377-2-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC116601/
https://www.ncbi.nlm.nih.gov/pubmed/12079501
http://dx.doi.org/10.1186/1471-2377-2-4

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