Načítá se...
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...
Uloženo v:
| Vydáno v: | Indian J Radiol Imaging |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer - Medknow
2019
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|