Reduced striatal [123I]FP-CIT binding in SCA2 patients without parkinsonism

Author:

Varrone Andrea,Salvatore Elena,De Michele Giuseppe,Barone Paolo,Sansone Valeria,Pellecchia Maria Teresa,Castaldo Imma,Coppola Giovanni,Brunetti Arturo,Salvatore Marco,Pappatà Sabina,Filla Alessandro

Funder

Amersham Health

Italian Ministry of University and FIRB

FIRB (Fondo per gli Investimenti nella Ricerca di Base)

Ministry of Health

Biological Markers in Par-kinson's Disease 2000, Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference17 articles.

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2. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families;Cancel;Hum Mol Genet,1997

3. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia;Geschwind;Am J Hum Genet,1997

4. Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine families;Zhou;Neurology,1998

5. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings;Orozco;J Neurol Sci,1989

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