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Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [(11)C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2) (Articolo in rivista)
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- Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [(11)C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2) (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Antonini A., Moresco R.M., Gobbo C., De Notaris R., Panzacchi A., Barone P., Bonifati V., Pezzoli G., Fazio F. (2002)
Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [(11)C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2)
in Neurological sciences (Testo stamp.)
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- Antonini A., Moresco R.M., Gobbo C., De Notaris R., Panzacchi A., Barone P., Bonifati V., Pezzoli G., Fazio F. (literal)
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- Titolo
- Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [(11)C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2) (literal)
- Abstract
- Neuroimaging studies of striatal dopamine transporters (DAT) have shown
that this measurement is a specific marker of dopaminergic degeneration in
patients with Parkinson's disease. However, little data is available in
subjects with early disease onset, particularly in those with autosomal
recessive parkinsonism. We measured striatal DAT binding in 10 patients
with early onset PD (onset <40 years) and in 10 with late onset PD (onset
>50 years) using PET and the tracer [(11)C]FECIT. One early onset subject
presented a mutation in the parkin gene consistent with autosomal
recessive parkinsonism. Data were compared with those of 15 control
subjects. We found a comparable decrement of striatal DAT binding in early
and late onset PD. Loss was widespread and bilateral in the patient
carrying the Park2 mutation, suggesting a different pattern of denervation
in these individuals.
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