360 results on '"Pappatà, Sabina"'
Search Results
2. Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosis
3. Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington’s disease
4. Singular cases of Alzheimer’s disease disclose new and old genetic “acquaintances”
5. Multimodal evaluation of the cerebrovascular reserve in Neurofibromatosis type 1 patients with Moyamoya syndrome
6. In vivo imaging of CNS microglial activation/macrophage infiltration with combined [18F]DPA-714-PET and SPIO-MRI in a mouse model of relapsing remitting experimental autoimmune encephalomyelitis
7. Different cortical excitability profiles in hereditary brain iron and copper accumulation
8. A new perspective for advanced positron emission tomography–based molecular imaging in neurodegenerative proteinopathies
9. Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families
10. Simultaneous resting-state FDG-PET/fMRI in Alzheimer Disease: Relationship between glucose metabolism and intrinsic activity
11. The role of molecular imaging in the frame of the revised dementia with Lewy body criteria
12. Movement Disorders: Focus on Parkinson’s Disease and Related Disorders
13. One novel GRN null mutation, two different aphasia phenotypes
14. Advances in SPECT Methodology
15. Apathy and striatal dopamine transporter levels in de-novo, untreated Parkinson's disease patients
16. Altered Patterns of Brain Glucose Metabolism Involve More Extensive and Discrete Cortical Areas in Treatment-resistant Schizophrenia Patients Compared to Responder Patients and Controls: Results From a Head-to-Head 2-[18F]-FDG-PET Study
17. Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutation
18. Myocardial 123I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations
19. Nonvascular Parkinsonism in Fabry Disease: Results From Magnetic Resonance and Dopamine Transporter Imaging.
20. Pathological laughter as onset symptom in atypical parkinsonisms
21. Anxiety is associated with striatal dopamine transporter availability in newly diagnosed untreated Parkinson's disease patients
22. Altered Patterns of Brain Glucose Metabolism Involve More Extensive and Discrete Cortical Areas in Treatment-resistant Schizophrenia Patients Compared to Responder Patients and Controls: Results From a Head-to-Head 2-[18F]-FDG-PET Study.
23. Correction to: The role of molecular imaging in the frame of the revised dementia with Lewy body criteria
24. Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD)
25. Dopamine transporter availability in motor subtypes of de novo drug-naïve Parkinson’s disease
26. GRN deletion in familial frontotemporal dementia showing association with clinical variability in 3 familial cases
27. Positron Emission Tomography with [11C]-Methyltacrine and [11C]-Physostigmine
28. PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family
29. Reduced cardiac 123I-metaiodobenzylguanidine uptake in patients with spinocerebellar ataxia type 2: a comparative study with Parkinson’s disease
30. Diagnostic challenges of Parkinsonism occurring in multiple sclerosis
31. Relationship between simultaneously acquired resting-state regional cerebral glucose metabolism and functional MRI: A PET/MR hybrid scanner study
32. Evaluation of age and sex-related metabolic changes in healthy subjects: An italian brain 18f-fdg pet study
33. Appropriate use criteria for amyloid PET imaging cannot replace guidelines: On behalf of the European Association of Nuclear Medicine
34. Nonvascular Parkinsonism in Fabry Disease: Results From Magnetic Resonance and Dopamine Transporter Imaging
35. Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome
36. Dysexecutive performance of healthy oldest old subjects on the Frontal Assessment Battery
37. Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability
38. SPECT imaging of GABAA/benzodiazepine receptors and cerebral perfusion in mild cognitive impairment
39. Complex phenotype in an Italian family with a novel mutation in SPG3A
40. Supratentorial and infratentorial damage in spinocerebellar ataxia 2: A diffusion-weighted MRI study
41. Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study
42. Comparison between a dual-head and a brain-dedicated SPECT system in the measurement of the loss of dopamine transporters with [123I]FP-CIT
43. Identification by [99mTc]ECD SPECT of anterior cingulate hypoperfusion in progressive supranuclear palsy, in comparison with Parkinson’s disease
44. Application of advanced brain positron emission tomography–based molecular imaging for a biological framework in neurodegenerative proteinopathies
45. Singular cases of Alzheimer’s disease disclose new and old genetic “acquaintances”
46. Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism
47. Voxel-based comparison of rCBF SPET images in frontotemporal dementia and Alzheimer's disease highlights the involvement of different cortical networks
48. The “eye of the tiger” sign in pure akinesia with gait freezing
49. Decreased carbon-11-flumazenil binding in early Alzheimer’s disease
50. Progression of Striatal and Extrastriatal Degeneration in Multiple System Atrophy: A Longitudinal Diffusion-Weighted MR Study
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