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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.

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Bibliografische gegevens
Hoofdauteur: J Gordon Millichap
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Pediatric Neurology Briefs Publishers 1996-04-01
Reeks:Pediatric Neurology Briefs
Onderwerpen:
Online toegang:https://www.pediatricneurologybriefs.com/articles/2535
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