2012
DOI: 10.1101/cshperspect.a009274
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Functional Neuroimaging in Parkinson's Disease

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Cited by 64 publications
(36 citation statements)
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References 199 publications
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“…PET and SPECT are molecular imaging methods that employ exogenous, radiolabeled agents (Hammoud et al, 2007; Niethammer et al, 2012; Price, 2012). In general, PET methods have better spatial resolution and sensitivity than SPECT.…”
Section: Neuroimaging Methodsmentioning
confidence: 99%
“…PET and SPECT are molecular imaging methods that employ exogenous, radiolabeled agents (Hammoud et al, 2007; Niethammer et al, 2012; Price, 2012). In general, PET methods have better spatial resolution and sensitivity than SPECT.…”
Section: Neuroimaging Methodsmentioning
confidence: 99%
“…In this regard, dopamine transporter (DAT) imaging with single-photon emission CT (DAT-SPECT) is a very useful approach, because it is sensitive for the detection of presynaptic dopaminergic neuron degeneration in the striatum (Kägi et al 2010a). None of these methods is able to distinguish PD from other causes of degenerative parkinsonism, but presynaptic dopamine imaging is normal in essential tremor, dystonic tremor, drug-induced, psychogenic tremor, and psychogenic parkinsonism (for more on details on functional imaging in PD please refer to the text by Niethammer et al 2012). In appropriate circumstances, genetic testing might be considered; whenever a pathogenic mutation is found, a definitive diagnosis of PD is achieved in vivo.…”
Section: Diagnosis Of Pd and Differential Diagnosis How To Diagnose Pdmentioning
confidence: 99%
“…In discussing this finding within the context of previous studies showing ventral thalamic activation during STN-DBS, the authors raise the possibility that activation of the neighboring STN may be the true source of some reported increases in thalamic blood flow and glucose metabolism. Interestingly, unmedicated Parkinson's patients at rest show hypermetabolism in the thalamus, part of the so-called Parkinson's Disease-Related Spatial Covariance Pattern (PDRP), which also includes GPi and primary motor cortex hyperactivity, as well as hypoactivity within supplementary motor cortices (Ma et al, 2007;Niethammer et al, 2012). In the context of the PDRP, the ventral thalamic inactivation reported by Geday et al may represent a normalization of pathological hyperactivity within the thalamocortical motor circuit.…”
Section: Circuit Modulations During Deep Brain Stimulation At the Stnmentioning
confidence: 99%