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Congenital biotinidase deficiency – MRI findings in two cases
Congenital biotinidase deficiency is a rare inborn error of metabolism that most commonly presents in infantile age group. Diffusion changes on magnetic resonance imaging (MRI) are sparsely described in the literature. We are presenting diffusion-weighted MRI findings in two confirmed cases of conge...
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| Publicado no: | Indian J Radiol Imaging |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6467045/ https://ncbi.nlm.nih.gov/pubmed/31000952 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijri.IJRI_159_18 |
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