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List of works by Anna Rita Giovagnoli

A new neurobehavioral phenotype of familial Creutzfeldt-Jakob disease: impaired theory of mind

scientific article published on 27 November 2018

A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype.

scientific article published in January 2009

Analyzing theory of mind impairment in patients with behavioral variant frontotemporal dementia

scientific article published on 11 May 2019

Blurring in patients with temporal lobe epilepsy: clinical, high-field imaging and ultrastructural study

scientific article published on June 22, 2012

Can telerehabilitation deal with cognitive disturbances in epilepsy?

scientific article published on 24 September 2020

Cognitive Abilities of Musicians

scientific article published on October 1, 2011

Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2.

scientific article published on 10 August 2006

Combining drug and music therapy in patients with moderate Alzheimer's disease: a randomized study

scientific article published on 17 March 2018

Drawing from memory in focal epilepsy: A cognitive and neural perspective

scientific article published on February 16, 2011

Gliomatosis cerebri. Report of a case with isolated amnesic disorders

scientific article published on September 1, 1992

Investigation of cognitive impairments in people with brain tumors

scientific article published on 06 March 2012

Self-reporting of everyday memory in patients with epilepsy: relation to neuropsychological, clinical, pathological and treatment factors

scientific article published on September 1, 1997

The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy

scientific article published on 28 January 2022

The fusiform gyrus and theory of mind: a case study

scientific article published on 21 November 2019

The understanding of mental states and the cognitive phenotype of frontal lobe epilepsy

scientific article published on 03 March 2020

Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene.

scientific article