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Cited by 269

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Hallervorden-Spatz Syndrome

Dooling, E. C., Schoene, W. C., Richardson, E. P.·1974·Archives of Neurology

Abstract

Two sisters with Hallervorden-Spatz syndrome (HSS) were treated with anti-Parkinson drugs. One showed the typical neuropathological lesions at death. The surviving sister has been treated with an iron-chelater without sustained effect, and with levodopa with improvement of motor abnormalities. Of 64 cases thought to represent HSS and studied post mortem, a group of 42 forms a distinct clinicopathologic entity. The remaining cases differ considerably from these, making their classification difficult at present. Hallervorden-Spatz syndrome may be the result of an inborn error of metabolism. Future studies of patients with HSS should include catecholamine analyses of cerebrospinal fluid and brain tissue and a search for viral infection, as iron studies have not been helpful.

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Crossref · 10.1001/archneur.1974.00490310072012

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Metadata

Authors
Dooling, E. C., Schoene, W. C., & Richardson, E. P.
Venue
Archives of Neurology
Published
1974-01-01
Volume
30
Issue
1
Pages
70-83
ISSN
0003-9942 (ISSN-L)
OpenAlex
W1974804543
Cited by
269
References
11
FWCI
2.99
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Hallervorden-Spatz Syndrome. https://app.cochat.ai/papers/10.1001/archneur.1974.00490310072012
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Dooling, E. C., Schoene, W. C., & Richardson, E. P. (1974). Hallervorden-Spatz Syndrome. Archives of Neurology. https://doi.org/10.1001/archneur.1974.00490310072012

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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