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.
I tiakina i:
| Kaituhi matua: | |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Pediatric Neurology Briefs Publishers
1996-04-01
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| Rangatū: | Pediatric Neurology Briefs |
| Ngā marau: | |
| Urunga tuihono: | https://www.pediatricneurologybriefs.com/articles/2535 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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