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....

Full description

Saved in:
Bibliographic Details
Published in:Neuroimage Clin
Main Authors: Hellewell, Sarah C., Welton, Thomas, Eisenhuth, Kate, Tchan, Michel C., Grieve, Stuart M.
Format: Artigo
Language:Inglês
Published: Elsevier 2021
Subjects:
Regular Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7814191/
https://ncbi.nlm.nih.gov/pubmed/33461111
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2020.102555
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items