Cinzia Tiloca

Milan, 20145, Italy

Last Updated: 09/26/2026

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Found 34 publications

Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patients.

Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patients.

Journal: Journal of neurology

Published: February 13, 2025

Coexistence of Amyotrophic Lateral Sclerosis and Alzheimer's Disease: Case Report and Review of the Literature.

Coexistence of Amyotrophic Lateral Sclerosis and Alzheimer's Disease: Case Report and Review of the Literature.

Journal: Journal of Alzheimer's disease : JAD

Published: September 11, 2023

Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study.

Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study.

Journal: Frontiers in aging neuroscience

Published: August 03, 2023

Correction to: Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.

Correction to: Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.

Journal: Journal of neurology

Published: March 13, 2023

TARDBP mutations in a cohort of Italian patients with Parkinson's disease and atypical parkinsonisms.

TARDBP mutations in a cohort of Italian patients with Parkinson's disease and atypical parkinsonisms.

Journal: Frontiers in aging neuroscience

Published: August 16, 2022

Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.

Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.

Journal: Journal of neurology

Published: August 09, 2022

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.

Journal: JAMA neurology

Published: August 30, 2021

Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis.

Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: May 30, 2020

CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum.

CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: December 20, 2019

PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival.

PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: November 04, 2018

Response to the commentary "The effect of C9orf72 intermediate repeat expansions in neurodegenerative and autoimmune diseases" by Biasiotto G and Zanella I.✰.

Response to the commentary "The effect of C9orf72 intermediate repeat expansions in neurodegenerative and autoimmune diseases" by Biasiotto G and Zanella I.✰.

Journal: Multiple sclerosis and related disorders

Published: October 02, 2018

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.

Journal: Neurobiology of aging

Published: April 18, 2018

Showing 1-12 of 34

Last Updated: 09/26/2026