PET in Huntington’s Disease
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-54307-4_30
Reference63 articles.
1. Andrews TC, Weeks RA, Turjanski N et al (1999) Huntington’s disease progression. PET and clinical observations. Brain 122(Pt 12):2353–2363
2. Antonini A, Leenders KL, Spiegel R et al (1996) Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington’s disease. Brain 119(Pt 6):2085–2095
3. Antonini A, Leenders KL, Eidelberg D (1998) [11C]raclopride-PET studies of the Huntington’s disease rate of progression: relevance of the trinucleotide repeat length. Ann Neurol 43:253–255
4. Bachoud-Levi AC, Deglon N, Nguyen JP et al (2000a) Neuroprotective gene therapy for Huntington’s disease using a polymer encapsulated BHK cell line engineered to secrete human CNTF. Hum Gene Ther 11:1723–1729
5. Bachoud-Levi AC, Remy P, Nguyen JP et al (2000b) Motor and cognitive improvements in patients with Huntington’s disease after neural transplantation. Lancet 356:1975–1979
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