Federica Sorrentino
Milan, Italy
Last Updated: 09/26/2026
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Found 13 publications
Klotho Gene Expression Is Decreased in Peripheral Blood Mononuclear Cells in Patients with Alzheimer's Disease and Frontotemporal Dementia.
Journal: Journal of Alzheimer's disease : JAD
Published: July 02, 2023
Predominant right temporal lobe atrophy: Clinical, neuropsychological and structural differences based on amyloid status.
Journal: European journal of neurology
Published: May 31, 2023
Association between enlarged perivascular spaces and cerebrospinal fluid aquaporin-4 and tau levels: report from a memory clinic.
Journal: Frontiers in aging neuroscience
Published: March 22, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect.
Journal: GeroScience
Published: October 17, 2022
Circulating Non-Coding RNA Levels Are Altered in Autosomal Dominant Frontotemporal Dementia.
Journal: International journal of molecular sciences
Published: October 12, 2022
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia.
Journal: Acta neuropathologica communications
Published: May 24, 2022
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation.
Journal: Alzheimer's research & therapy
Published: February 19, 2022
Differences in Sex Distribution Between Genetic and Sporadic Frontotemporal Dementia.
Journal: Journal of Alzheimer's disease : JAD
Published: October 11, 2021
Niemann-Pick Type C 1 (NPC1) and NPC2 Gene Variability in Demented Patients with Evidence of Brain Amyloid Deposition.
Journal: Journal of Alzheimer's disease : JAD
Published: August 23, 2021
Analysis of C9orf72 Intermediate Alleles in a Retrospective Cohort of Neurological Patients: Risk Factors for Alzheimer's Disease?
Journal: Journal of Alzheimer's disease : JAD
Published: May 03, 2021
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation.
Journal: European journal of neurology
Published: July 03, 2020
Last Updated: 09/26/2026