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Predicting amyloid status in corticobasal syndrome using modified clinical criteria, magnetic resonance imaging and fluorodeoxyglucose positron emission tomographyAtypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansionImaging markers for Alzheimer disease: which vs howExisting Pittsburgh Compound-B positron emission tomography thresholds are too high: statistical and pathological evaluationEvaluating and treating neurobehavioral symptoms in professional American football players: Lessons from a case series.Executive dysfunctionClinicopathological correlations in corticobasal degenerationAdvancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria.Abeta amyloid and glucose metabolism in three variants of primary progressive aphasiaSeizures and epileptiform activity in the early stages of Alzheimer diseaseEarly-onset Alzheimer's disease versus frontotemporal dementia: resolution with genetic diagnoses?Cerebrospinal fluid neurofilament concentration reflects disease severity in frontotemporal degeneration.Communicating mild cognitive impairment diagnoses with and without amyloid imaging.Seizures in corticobasal degeneration: a case report.Sporadic corticobasal syndrome due to FTLD-TDP.Increased metabolic vulnerability in early-onset Alzheimer's disease is not related to amyloid burdenDonepezil-associated bradyarrhythmia in a patient with dementia with Lewy bodies (DLB)Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease.Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.Cognition, glucose metabolism and amyloid burden in Alzheimer's disease.Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseasesShared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.Divergent CSF τ alterations in two common tauopathies: Alzheimer's disease and progressive supranuclear palsyProdromal posterior cortical atrophy: clinical, neuropsychological, and radiological correlation.Anomalous functional language lateralization in semantic variant PPAEarly 11C-PIB frames and 18F-FDG PET measures are comparable: a study validated in a cohort of AD and FTLD patientsRelationships between β-amyloid and functional connectivity in different components of the default mode network in agingTau, amyloid, and hypometabolism in a patient with posterior cortical atrophy.A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaquesBehavioral variant frontotemporal dementia with corticobasal degeneration pathology: phenotypic comparison to bvFTD with Pick's disease.Not quite PIB-positive, not quite PIB-negative: slight PIB elevations in elderly normal control subjects are biologically relevantCerebrospinal fluid biomarkers and cerebral atrophy in distinct clinical variants of probable Alzheimer's disease.Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysis.Amyloid imaging, risk disclosure and Alzheimer's disease: ethical and practical issues.Amyloid imaging in the differential diagnosis of dementia: review and potential clinical applications.Prevalence of amyloid PET positivity in dementia syndromes: a meta-analysisMapping the Progression of Atrophy in Early- and Late-Onset Alzheimer's DiseaseProgression of Microstructural Degeneration in Progressive Supranuclear Palsy and Corticobasal Syndrome: A Longitudinal Diffusion Tensor Imaging Study.The behavioural/dysexecutive variant of Alzheimer's disease: clinical, neuroimaging and pathological features.Amyloid in dementia associated with familial FTLD: not an innocent bystander.
P50
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P50
name
Gil D Rabinovici
@en
type
label
Gil D Rabinovici
@en
prefLabel
Gil D Rabinovici
@en