Barbara Borroni
Barbara Borroni
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Criteria for the diagnosis of corticobasal degeneration
MJ Armstrong, I Litvan, AE Lang, TH Bak, KP Bhatia, B Borroni, AL Boxer, ...
Neurology 80 (5), 496-503, 2013
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET
L Mosconi, D Perani, S Sorbi, K Herholz, B Nacmias, V Holthoff, E Salmon, ...
Neurology 63 (12), 2332-2340, 2004
Progranulin deficiency promotes circuit-specific synaptic pruning by microglia via complement activation
H Lui, J Zhang, SR Makinson, MK Cahill, KW Kelley, HY Huang, Y Shang, ...
Cell 165 (4), 921-935, 2016
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
JD Rohrer, JM Nicholas, DM Cash, J van Swieten, E Dopper, L Jiskoot, ...
The Lancet Neurology 14 (3), 253-262, 2015
Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease
D Anchisi, B Borroni, M Franceschi, N Kerrouche, E Kalbe, ...
Archives of neurology 62 (11), 1728-1733, 2005
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
JD Rohrer, T Lashley, JM Schott, JE Warren, S Mead, AM Isaacs, J Beck, ...
Brain 134 (9), 2565-2581, 2011
Incidence of and risk factors for hallucinations and delusions in patients with probable AD
JS Paulsen, DP Salmon, LJ Thal, R Romero, C Weisstein–Jenkins, ...
Neurology 54 (10), 1965-1971, 2000
A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ...
Human mutation 34 (2), 363-373, 2013
Mutation within TARDBP leads to Frontotemporal Dementia without motor neuron disease
B Borroni, C Bonvicini, A Alberici, E Buratti, C Agosti, S Archetti, A Papetti, ...
Human mutation 30 (11), E974-E983, 2009
Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence
V Garibotto, B Borroni, E Kalbe, K Herholz, E Salmon, V Holtoff, S Sorbi, ...
Neurology 71 (17), 1342-1349, 2008
Frontotemporal dementia and its subtypes: a genome-wide association study
R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ...
The Lancet Neurology 13 (7), 686-699, 2014
Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status
L Piccio, Y Deming, JL Del-Águila, L Ghezzi, DM Holtzman, AM Fagan, ...
Acta neuropathologica 131 (6), 925-933, 2016
Platelet APP, ADAM 10 and BACE alterations in the early stages of Alzheimer disease
F Colciaghi, E Marcello, B Borroni, M Zimmermann, C Caltagirone, ...
Neurology 62 (3), 498-501, 2004
Synapse-associated protein-97 mediates α-secretase ADAM10 trafficking and promotes its activity
E Marcello, F Gardoni, D Mauceri, S Romorini, A Jeromin, R Epis, ...
Journal of Neuroscience 27 (7), 1682-1691, 2007
α-Secretase ADAM10 as Well as α APPs Is Reduced in Platelets and CSF of Alzheimer Disease Patients
F Colciaghi, B Borroni, L Pastorino, E Marcello, M Zimmermann, ...
Molecular medicine 8 (2), 67-74, 2002
Action and object naming in frontotemporal dementia, progressive supranuclear palsy, and corticobasal degeneration.
M Cotelli, B Borroni, R Manenti, A Alberici, M Calabria, C Agosti, ...
Neuropsychology 20 (5), 558, 2006
Diffusion tensor imaging and voxel based morphometry study in early progressive supranuclear palsy
A Padovani, B Borroni, SM Brambati, C Agosti, M Broli, R Alonso, P Scifo, ...
Journal of Neurology, Neurosurgery & Psychiatry 77 (4), 457-463, 2006
Combined 99mTc-ECD SPECT and neuropsychological studies in MCI for the assessment of conversion to AD
B Borroni, D Anchisi, B Paghera, B Vicini, N Kerrouche, V Garibotto, ...
Neurobiology of aging 27 (1), 24-31, 2006
Neurofilament light chain: a biomarker for genetic frontotemporal dementia
LH Meeter, EG Dopper, LC Jiskoot, R Sanchez‐Valle, C Graff, L Benussi, ...
Annals of clinical and translational neurology 3 (8), 623-636, 2016
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