Sabina Pappata

Affiliations: 
CNR, New Rochelle, NY, United States 
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"Sabina Pappata"
Mean distance: 15.98 (cluster 23)
 
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Publications

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De Rosa A, Pellegrino T, Pappatà S, et al. (2015) Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism. Parkinsonism & Related Disorders
De Rosa A, Pellegrino T, Pappatà S, et al. (2015) Myocardial (123)I-metaiodobenzylguanidine scintigraphy in patients with homozygous and heterozygous parkin mutations. Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology
Aiello M, Salvatore E, Cachia A, et al. (2015) Relationship between simultaneously acquired resting-state regional cerebral glucose metabolism and functional MRI: a PET/MR hybrid scanner study. Neuroimage. 113: 111-21
Santangelo G, Vitale C, Picillo M, et al. (2015) Apathy and striatal dopamine transporter levels in de-novo, untreated Parkinson's disease patients. Parkinsonism & Related Disorders. 21: 489-93
Pellecchia MT, Picillo M, Santangelo G, et al. (2015) Cognitive performances and DAT imaging in early Parkinson's disease with mild cognitive impairment: a preliminary study. Acta Neurologica Scandinavica. 131: 275-81
Vicidomini C, Panico M, Greco A, et al. (2015) In vivo imaging and characterization of [(18)F]DPA-714, a potential new TSPO ligand, in mouse brain and peripheral tissues using small-animal PET. Nuclear Medicine and Biology. 42: 309-16
Peluso S, De Rosa A, Antenora A, et al. (2015) Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. Parkinsonism & Related Disorders. 21: 156-8
Zinnhardt B, Viel T, Wachsmuth L, et al. (2015) Multimodal imaging reveals temporal and spatial microglia and matrix metalloproteinase activity after experimental stroke Journal of Cerebral Blood Flow and Metabolism
Perani D, Della Rosa PA, Cerami C, et al. (2014) Validation of an optimized SPM procedure for FDG-PET in dementia diagnosis in a clinical setting. Neuroimage. Clinical. 6: 445-54
Olgiati S, De Rosa A, Quadri M, et al. (2014) PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family. Neurogenetics. 15: 183-8
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