The 3-Nitropropionic Acid Model of Huntington’s Disease
Author:
Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-59259-692-8_10.pdf
Reference51 articles.
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2. Kuhl DE, Phelps ME, Markham CH, Metter EJ, Riege WH, Winter P. Cerebral metabolism and atrophy in Huntington’s disease determined by 18FDG and computerised tomography. Ann Neurol 1982; 12: 425–434.
3. Sax DS, Powser R, Kim A, Bhatia R, Cupples LA, Myers RH. Evidence of cortical metabolic dysfunction in early Huntington’s disease by single-photonemission computed tomography. Mov Disord 1996; 11: 671–677.
4. Martin WRW, Clark C, Ammann W, Stoessl AJ, Shytbel W, Hayden MR. Cortical glucose metabolism in Huntington’s disease. Neurology 1992; 42: 223–229.
5. Antonini A, Leenders KL, Spiegel R, et al. Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington’ s disease. Brain 1996; 119: 2085–2095.
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