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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2002
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| 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 |