Diffusion kurtosis imaging detects subclinical white matter abnormalities in Phenylketonuria

OBJECTIVE: Phenylketonuria (PKU) is an autosomal recessive disorder whereby deficiencies in phenylalanine metabolism cause progressive neurological dysfunction. Managing PKU is challenging, with disease monitoring focussed on short-term phenylalanine control rather than measures of neuronal damage....

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Detalles Bibliográficos
Autores principales: Hellewell, Sarah C., Welton, Thomas, Eisenhuth, Kate, Tchan, Michel C., Grieve, Stuart M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814191/
https://www.ncbi.nlm.nih.gov/pubmed/33461111
http://dx.doi.org/10.1016/j.nicl.2020.102555

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814191/
https://www.ncbi.nlm.nih.gov/pubmed/33461111
http://dx.doi.org/10.1016/j.nicl.2020.102555

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