Excitotoxic Lesions of the Neostriatum as an Animal Model of Huntington’s Disease
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4899-1447-7_8
Reference292 articles.
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2. Aquidonius, S.M., Eckernas, S.A., and Sundwall, A., 1975, Regional distribution of choline acetyltransferase in the human brain: Changes in Huntington’s chorea, J. Neurol. Neurosurg. Psychiatry 38:669–677.
3. Araki, M., McGeer, P.L., and McGeer, E.G., 1985, Striatonigral and pallidonigral pathways studied by a combination of retrograde horseradish peroxidase tracing and pharmacohistochemical method for gamma aminobutyric acid transaminase, Brain Res. 331:17–24.
4. Arregui, A., Bennett, J.P., Jr., Bird, E.D., Yamamura, H.I., Iversen, L.I., and Snyder, S.H., 1977, Huntington’s chorea: Selective depletion of activity of angiotensin converting enzyme in the corpus striatum, Ann. Neurol. 2: 294–298.
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