Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stages - Varani, K; Bachoud-Lévi, A-C; Mariotti, C; Tarditi, A; Abbracchio, M P; Gasperi, V; Borea, P A; Dolbeau, G; Gellera, C; Solari, A; Rosser, A; Naji, J; et al. (Neurobiology of disease, 2007)
Keywords: Adolescent; Adult; Age of Onset; Aged; Biomarkers - metabolism; Cell Polarity - physiology; Female; Friedreich Ataxia - genetics; Friedreich Ataxia - metabolism; Humans; Huntington Disease - drug therapy; Huntington Disease - genetics; Huntington Disease - metabolism; Lymphocytes - metabolism; Male; Membrane Fluidity - physiology; Middle Aged; Peptides - genetics; Peptides - metabolism; Receptors, Adrenergic, alpha-2 - genetics; Receptors, Adrenergic, alpha-2 - metabolism; Spinocerebellar Ataxias - genetics; Spinocerebellar Ataxias - metabolism; Trinucleotide Repeats