Hallervorden-Spatz Disease: Clinicopathology
Clinical and pathological features of familial late infantile Hallervorden-Spatz disease (HSD) are reported in two sisters, one of whom died at 11 years, from the Institute for Neurological Sciences, University of Siena, Italy.
Bewaard in:
| Hoofdauteur: | |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Pediatric Neurology Briefs Publishers
1996-04-01
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| Reeks: | Pediatric Neurology Briefs |
| Onderwerpen: | |
| Online toegang: | https://www.pediatricneurologybriefs.com/articles/2535 |
| Tags: |
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