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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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| Publicado no: | Neuroimage Clin |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2021
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| Assuntos: | |
| Acesso em linha: | 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 |
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